Anti-Aging Activity and Modes of Action of Compounds from Natural Food Sources
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Key Laboratory of Biomedical Materials of Zhangjiakou, College of Lab Medicine, Hebei North University, Zhangjiakou 075000, China
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College of Life and Geographic Sciences, Kashi University, Kashi 844000, China
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Xinjiang Key Laboratory of Biological Resources and Ecology of Pamirs Plateau, Kashi 844000, China
4
Department of Marine Biology, Institute of Evolution & Marine Biodiversity, Ocean University of China, 5 Yushan Road, Qingdao 266003, China
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Author to whom correspondence should be addressed.
Biomolecules 2023, 13(11), 1600; https://doi.org/10.3390/biom13111600
Submission received: 4 September 2023
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Revised: 21 October 2023
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Accepted: 28 October 2023
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Published: 31 October 2023
Abstract
:Aging is a natural and inescapable phenomenon characterized by a progressive deterioration of physiological functions, leading to increased vulnerability to chronic diseases and death. With economic and medical development, the elderly population is gradually increasing, which poses a great burden to society, the economy and the medical field. Thus, healthy aging has now become a common aspiration among people over the world. Accumulating evidence indicates that substances that can mediate the deteriorated physiological processes are highly likely to have the potential to prolong lifespan and improve aging-associated diseases. Foods from natural sources are full of bioactive compounds, such as polysaccharides, polyphenols, carotenoids, sterols, terpenoids and vitamins. These bioactive compounds and their derivatives have been shown to be able to delay aging and/or improve aging-associated diseases, thereby prolonging lifespan, via regulation of various physiological processes. Here, we summarize the current understanding of the anti-aging activities of the compounds, polysaccharides, polyphenols, carotenoids, sterols, terpenoids and vitamins from natural food sources, and their modes of action in delaying aging and improving aging-associated diseases. This will certainly provide a reference for further research on the anti-aging effects of bioactive compounds from natural food sources.
Keywords:
foods; bioactive compounds; polysaccharides; polyphenols; carotenoids; sterols; terpenoids; vitamins; anti-aging; lifespan
1. Introduction
We humans all age without exception. Aging is a natural and inescapable phenomenon characterized by a progressive deterioration of physiological functions, leading to increased vulnerability to chronic diseases and death. With economic and medical development, the lifespan of human beings continues to grow throughout the world. It is estimated that there will be more than 795 million people aged 65 years old or over globally by 2023 [1], and this figure will reach 994 million by 2030 and 1.6 billion by 2050, respectively [2]. Aging is usually accompanied by many age-related diseases such as cancer, cardiovascular disease, metabolic disease, kidney disease, liver disease, neurodegenerative disease, autoimmune disease and inflammation, and dysbiosis (Figure 1), as well as other chronic diseases, creating pressure on social health insurances and causing a large economic burden in most countries. Thus, healthy aging has now become a common aspiration among people all over the world.
Aging and anti-aging have attracted curiosity and inspired imagination throughout the history of humankind. In both Eastern and Western civilizations, achieving longevity while postponing aging, or immortality, had long been a fantasy of certain ancient people [3,4]. With the tremendous progress of aging studies over the past three decades, today, anti-aging appears to be no longer a fantasy because the rate of aging can be controlled, at least to some extent, by genetic pathways and biochemical processes conserved in evolution [5,6,7,8]. Numerous theories have been proposed to explain the aging progress, such as mitochondrial free radical theory [9,10], telomere theory [11,12], DNA damage theory [13] and error theory [14]. Broadly speaking, aging theories can be categorized into two major groups: (1) program theory, which suggests that aging is not a random occurrence but instead is genetically programmed in our genetic information, and (2) wear-and-tear theory, proposed by Weismann in 1889 [15], which proposes that aging occurs when cells and tissues are worn down by risk factors over the years. Whatever the theory, aging is generally accompanied by the impairment of various physiological processes such as mitochondrial dysfunction, decline in immunity, slowing down of basal metabolism, imbalance of apoptosis and autophagy, alteration of intestinal flora, reduction in activities of antioxidant enzymes, cellular senescence, and so on [16,17,18,19]. In accordance, substances that can mediate the physiological processes above are highly likely to have the potential to prolong lifespan and improve aging-associated diseases.
Foods from natural sources are full of bioactive compounds such as polysaccharides, polyphenols, carotenoids, sterols, terpenoids and vitamins [20,21]. These bioactive compounds and their derivatives have been shown to be able to delay aging and/or improve aging-associated diseases, thereby prolonging lifespan [22,23,24], via the regulation of various physiological processes, including antioxidant reactions, anti-inflammatory response, immunity, telomere activation, anti-apoptosis and mitochondrial repair, etc. [25,26]. Below, we will discuss the state-of-the-art understanding of the anti-aging activities of the compounds, polysaccharides, polyphenols, carotenoids, sterols, terpenoids and vitamins from natural food sources, and their modes of action in delaying aging and improving aging-associated diseases.
2. Anti-Aging Effects of Compounds from Food Sources
Bioactive compounds from natural food sources refer to the extra-nutritional constituents that are typically present in small quantities in foods. Many bioactive compounds have been discovered. These compounds, including polysaccharides, polyphenols, carotenoids, sterols, terpenoids and vitamins, are being intensively studied to evaluate their effects on health, and many of them appear to have anti-aging activities.
2.1. Polysaccharides
Polysaccharides are macromolecules consisting of tens to thousands of monosaccharides that are linked by α-1,4, β-1,3, α-1,6 or β-1,6 glycosidic bonds. It has been shown that the polysaccharides with β-(1,3)-D-glucan main-chain structure usually have important bioactive activity [27]. There exist two groups of polysaccharides, homopolysaccharide and heteropolysaccharide, with the former composed of the same monosaccharide, and the latter two or more different monosaccharides. Polysaccharides occur widely present in plants, algae, fungi and bacteria. Many studies have demonstrated that some polysaccharides and their derivatives, extracted from natural food sources, show various pharmacological effects, such as anti-diabetic, anti-tumor, cholesterol-lowering, wound-healing, anti-inflammatory, antioxidative, immune-modulatory and even anti-aging activities [28,29,30]. In addition, polysaccharides have unique advantages in terms of side effects and long-term use due to their low cytotoxicity, which is expected to contribute to the development of novel anti-aging drugs or supplements [30]. Here, we describe the anti-aging activity of polysaccharides from food sources and their modes of action (Table 1).
2.1.1. Plant Polysaccharides
Many studies have demonstrated that plant polysaccharides often display anti-aging effects. Chinese wolfberry Lycium barbarum serves as both medicine and food. L. barbarum polysaccharide (LBP), the main bioactive substance of wolfberry, was shown to be able to prolong the lifespan of the fruit fly Drosophila melanogaster and the nematode Caenorhabditis elegans [31,32], and to reverse the estrogen deficiency-induced learning and memory impairments of ovariectomized mice [33]. Moreover, LBP was found to partially protect against UVB-induced photodamage [34] as well as the PM2.5-induced mitophagy and mitochondrial damage of the human keratinocyte HaCaT cells [35], showing anti-skin-aging activity. The edible and medicinal ginseng Chuanminshen violaceum polysaccharides (CVPs) were also found to increase the body weight and spleen index of D-galactose (D-gal)-induced-aging mice, suggesting the presence of anti-aging activity [37], and the polysaccharides from ginsenoside residues (GRPs) were found to extend the lifespan of C. elegans [38]. Similarly, sweet tea Rubus suavissmus polysaccharides (STP-60a) were demonstrated to increase the mean lifespan of C. elegans, reduce the lipofuscin (LF) level and improve the survival rate of worms under heat stress and oxidative stress [39].
2.1.2. Algal Polysaccharides
Edible marine algae are rich in bioactive polysaccharides that are widely used in the food and chemical industries as well as in medicine and healthcare due to their benefits to health [45,61]. The kelp Laminaria japonica, a marine macroalga, is a common and important sea food for human consumption. L. japonica polysaccharide (LJP) was shown to possess an anti-aging effect. LJP could enhance the acute oxidation resistance of C. elegans when exposed to high temperatures, prolong the lifespan of worms, and decrease the accumulation of malondialdehyde (MDA), LF and reactive oxygen species (ROS) [45]. The laver Pyropia haitanensis, a red alga, is another common sea food. The P. haitanensis polysaccharide, porphyrin, was able to significantly ameliorate the learning and memory impairment in Alzheimer’s disease (AD)-model mice, to increase choline acetyltransferase (ChAT) activity, and to decrease acetylcholinesterase (AChE) activity in the cortical and hippocampal tissue of AD-model mice [46]. The asparagus Gracilaria lemaneiformis, a brown seaweed, is usually eaten as a vegetable. G. lemaneiformis polysaccharides (GPs) could extend the mean lifespan of C. elegans and significantly increase the reproduction duration of worms [47].
2.1.3. Fungal Polysaccharides
Edible fungi contain rich bioactive components that have both nutritional and medicinal values, thus making them a potent dietary supplement to attenuate aging and prevent age-related diseases in humans [54,62]. Increasing evidence has shown that polysaccharides are one of the main bioactive components that exhibit anti-aging activity in edible fungi [54,63]. For example, the polysaccharides derived from the bolete Lanmaoa asiatica (FLAPs) and the yellow mushroom Hohenbuehelia serotina (FHSPs), and the β-glucans derived from the maitake Grifola frondosa (GFGs) and the monkey head mushroom Hericium erinaceus (HEGs), were all able to prolong the lifespans of C. elegans [51] and D. melanogaster [52], respectively. The intracellular zinc polysaccharides (IZPs) of G. frondosa not only decreased the MDA content but also ameliorated the anile condition of D-gal-induced-aging mice [53]. It was also shown that the sulfated polysaccharides of the golden mushroom Flammulina velutipes (SFPs) reversed the D-gal-induced weight loss and tissue damage of aging mice [54], and the polysaccharides of the common cultivated mushroom Agaricus bisporus (WMPs) improved the locomotor activity and spatial and recognition memory of the aging mice [55]. Interestingly, WMPs extracted by different methods such as acidic-extraction (AcAPs) and enzyme-assisted extraction (EnAPs) all displayed potential anti-aging effects against D-gal-induced-aging diseases on the liver, kidney, brain and skin [56,57].
2.2. Polyphenols
Polyphenols are the secondary metabolites of plants, characterized by at least two phenyl rings and one or more hydroxyl substituents [64]. Based on whether their chemical structure contains sugar or not, and whether it is hydrolyzed or condensed, polyphenols are usually divided into five groups: phenolic acids, flavonoids, stilbenes, lignans and tannins [65]. Polyphenols are found in high quantities in beverages such as tea and red wine, in vegetables such as red pepper, eggplant, garlic and carrot, and in fruits such as grape and mulberry [66,67]. Marine algae also contain rich polyphenols [68]. Previous studies have shown that polyphenols possess multiple biological effects, including antioxidant, anti-aging, anti-inflammatory, neuroprotective, anti-cancer and anti-diabetic activities [69,70,71,72]. For example, walnuts and their by-products, rich in phenolic components, were shown to decrease the levels of ROS and inflammatory cytokines, modulate the Nrf2/EpRE, PI3K/Akt/mTOR and NF-κB signaling pathways, prevent mitochondrial dysfunction, and regulate energy homeostasis, thus presenting anti-aging potential [73]. Here, we describe the anti-aging activity of polyphenols, including phenolic acids, flavonoids, stilbenes, lignans and tannins from natural food sources, and their possible anti-aging mechanisms (Table 2).
2.2.1. Phenolic Acids
Phenolic acids contain an aromatic benzene ring and a carboxylic acid group and mainly exist in wine, sorghum, dried dates, blackberries, apple juice, olives, chicory and black tea. Phenolic acids are subdivided into hydroxybenzoic acid and hydroxycinnamic acid [97]. Previous studies have reported that phenolic acids display prominent anti-aging effects. Chlorogenic acid (CGA), a predominant class of phenolic acids extracted from coffee and tea, could extend the lifespan of C. elegans by up to 20.1%, delay the age-related decline of body movement, and improve stress resistance. Moreover, CGA activated the Forkhead box O (FoxO) transcription factor DAF-16, heat shock transcription factor-1 (HSF-1), SKiNhead-1 (SKN-1), and hypoxia-inducible factor-1 (HIF-1), and thus extended the lifespan of C. elegans mainly via DAF-16 in the insulin/IGF-1 signaling (IIS) pathway [74]. Similarly, p-Coumaric acid, a kind of hydroxycinnamic acid abundant in peanuts, carrots, and garlic, could increase the survival of C. elegans under oxidative and osmosis-stressed conditions. In addition, treatment with p-Coumaric acid could result in a significant reduction of intercellular ROS levels and a marked increase in antioxidant capacity through the regulation of skn-1, an ortholog of the nuclear factor erythroid 2-related factor 2 (Nrf2) transcriptional factor [75].
2.2.2. Flavonoids
Flavonoids are subdivided into flavonols, flavanones, isoflavones, flavones, anthocyanins, and flavan-3-ols according to their chemical structure and have all been shown to possess anti-aging activity. Quercetin, belonging to the flavonols, has been demonstrated to have a positive effect on longevity and stress resistance in various animal models. It was shown that feeding with quercetin prolonged lifespan, suppressed age-related motility retardation, improved motility recovery after heat stress, and reduced the production of both intercellular and mitochondrial ROS in C. elegans through the modulation of the insulin-like and mitogen-activated protein kinase (MAPK) pathways [77]. It was also shown that a diet containing quercetin or rutin diminished several early signs of AD-model mice, and the administration of quercetin or rutin increased the glutathione/oxidized glutathione (GSH/GSSG) ratio, diminished the MDA level, and favored the enzyme antioxidant capacity. Moreover, exposure to quercetin or rutin could diminish amyloid precursor protein (APP) synthesis, β-site APP-cleaving enzyme 1 (BACE1) activity, and the expression of the inflammatory markers interleukin-1β (IL-1β) and interferon-γ (IFN-γ) in AD mice [79].
Apigenin, luteolin and genkwanin are other important classes of flavonoids. They were found to possess antioxidant and anti-inflammatory properties capable of inhibiting ROS production and carcinogenesis and modulating the activity of the enzymes involved in neurological function, thereby contributing to anti-aging action [98,99,100]. For example, apigenin was shown to reduce ROS and MDA levels via enhancing activities of the antioxidant enzymes catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPX), as well as upregulating the levels of antioxidant response proteins, such as Nrf2 and AMPK [98]. An in-vitro study indicated that apigenin prevented the injury response of lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophage cells by enhancing the reduction of NO. Apigenin also decreased the levels of pro-inflammatory cytokines TNF-α, IL-18, and IL-6; downregulated the expression of cyclooxygenase (COX-2) and inducible nitric oxide synthase (iNOS); and reduced intracellular ROS production [98]. In addition, apigenin was able to inhibit the activity of intracellular cell-adhesion molecules (ICAMS), monocyte inflammatory protein (MIP-1α), and monocyte chemotactic protein (MCP-1α) inhibitors induced by LPS, resulting in an anti-inflammatory response [101,102].
Anthocyanins are found in a wide variety of colored vegetables, fruits, and cereal, especially in various berry fruits such as bilberries, blueberries, blackberries, blackcurrants, chokeberries, strawberries, and elderberries [80,103]. It was found that anthocyanin extracted from purple wheat extended the mean lifespan of wild-type nematodes and mev-1 (hn1) mutants, which are sensitive to oxidative stress, by up to 10.5 and 9.2%, respectively, through the activation of DAF-16/FoxO transcription factors [80]. Anthocyanins from the honeysuckle Lonicera pallasii were also shown to prolong the median and maximum lifespan of the fruit fly by up to 8% and enhance the integrity of the intestinal barrier. Interestingly, all these effects were accompanied by the increased expression of Hif1 (pro-longevity gene) and decreased expression of Keap1 (anti-longevity gene). RNA interference-mediated experiments indicated that the positive effects inspired by anthocyanin administration were associated with Sirt6 activation [81].
2.2.3. Stilbenes
The most important representative of stilbene compounds is resveratrol, which is mainly present in grape peels, grape seeds, blueberries, peanuts, red wine and some traditional Chinese herbal medicines such as rhubarb Rheum palmatum and giant knotweed Polygonum cuspidatum [104,105,106]. Resveratrol is usually recommended as a dietary supplement to maintain redox balance and delay aging [107]. Previous studies have shown that resveratrol could extend the lifespans of various organisms, including yeast, nematodes, fruit flies, Mexican fruit flies, turquoise killifish and mice [72]. Resveratrol was revealed to prolong the lifespan of both male and female adult fruit flies through scavenging ROS and neuroprotection [83]. Resveratrol also prolonged the lifespan, improved the cognitive ability, and attenuated the aging-related histological markers of aged annual fish Nothobranchius guentheri (N. guentheri) [84], and delayed ovarian aging in N. guentheri by alleviating inflammation and endoplasmic reticulum (ER) stress through Sirt1/Nrf2 [85]. Interestingly, resveratrol not only extended the lifespan but also delayed the worsening of the motor phenotype of HtrA2 knockout mice [86].
2.2.4. Lignans
Lignans, phenolic dimers possessing a 2,3-dibenzylbutane structure, are found in legumes, grains, seeds and vegetable oils. Sesamin is a major lignan constituent of sesame and has anti-aging activity. It was reported that sesamin could prolong the lifespan of nematodes and reduce amyloid-β toxicity [91]. Sesamin was also able to extend the lifespan of the mev-1 mutant nematodes that produced abundant superoxide anions [92]. Moreover, sesamin was capable of making nematodes more resistant to infection by the pathogen Legionella pneumophila and more resistant to oxidative stressors such as paraquat and H2O2 treatment [92].
2.2.5. Tannins
Tannic acid (TA) and ellagic acid (EA) are two common tannins with anti-aging effects. It was shown that exposure to low concentrations of TA exhibited potent life-prolonging properties in C. elegans and enhanced both thermal-stress resistance and oxidative-stress resistance [93]. EA was also able to prolong the lifespan of nematodes [94]. Moreover, oenothein B (OEB), a dimeric hydrolyzable tannin of macrocyclic structure [95], and pentagalloyl glucose (PGG), a xanthoyl tannin [96], both induced the lifespan extension of nematodes through the regulation of the IIS and dietary restriction (DR) pathway and the mitochondrial electron transport chain. Recently, urolithin A, a kind of intestinal microbiota metabolite of ellagitannin-rich foods, was also shown to exhibit anti-aging activities by enhancing stress resistance, reducing mitochondrial function decrease, and inhibiting the age-related decrease in C. elegans [42].
2.3. Carotenoids
Carotenoids are a group of pigments that mainly exist in fruits (e.g., pineapple and papaya), flowers (e.g., marigold flower and sunflower), vegetables (e.g., tomato and carrot), algae (e.g., microalgae and brown algae) and seafood (e.g., krill and fish). Organisms containing carotenoids may present yellow, orange or red colors. Carotenoids comprise eight isoprene units, resulting in multiple cis- and trans-isomers, with the latter being more abundant in nature [108] (p. 379) and [109] (p. 681). Carotenoids are divided into two groups, carotenes and xanthophylls, on the basis of their chemical structure. Common carotenes include α-carotene, β-carotene, γ-carotene and lycopene, which are highly soluble in organic solvents [108]. Xanthophylls are the oxygenated derivatives of carotenes. Common xanthophylls are astaxanthin, fucoxanthin, lutein, violaxanthin and canthaxanthin, which are soluble in polar solvents and organic solvents [108,109]. Previous studies have shown that carotenoids have multiple biological effects, including immune-system modulation, cell communication, antioxidant activity, anti-aging effects, anti-inflammatory response, anti-angiogenic activity and antiproliferative activity [110,111]. Here, we describe the anti-aging activities of carotenes and xanthophylls from natural food source and their possible anti-aging mechanisms (Table 3).
2.3.1. Carotenes
β-Carotene is an antioxidant that has been shown to be a cancer suppressor and an anti-inflammatory agent in various animal and cell models [126]. Recently, β-carotene has been reported to possess an anti-aging effect [112]. Exposure to β-carotene reduced the activity of SA-β-Gal, the production of P21, P16 and P53, and levels of pro-inflammatory factors such as IL-1β, IL-6, and tumor necrosis factor-α (TNF-α), accompanied by the downregulation of nuclear factor-kappaB (NF-κB) phosphorylation level, in the senescent mesenchymal stem cells (MSCs) model induced by H2O2. Exposure to β-carotene also reduced the levels of ROS and MDA but increased the level of SOD. Moreover, exposure to β-carotene not only enhanced learning and memory ability, alleviated anxiety, and improved the physical fitness of aged Y-maze mice, but it also slowed down the aging of tissues and organs and diminished the level of tissue and organ fibrosis. Furthermore, a prospective study of 960 participants of the Memory and Aging Project indicated that in older adults (over 60 years old), the intake of dark green vegetables rich in β-carotene, α-tocopherol, and phylloquinone benefited certain domains of cognition, including learning and memory [127]. All these facts indicate that β-carotene has anti-aging effects. It appears that β-carotene exerts the anti-aging effect through the regulation of the lysine acetyltransferase 7 (KAT7)-P15 (a cyclin that induces a G1-phase cell-cycle arrest) axis [112].
Lycopene is the primary phytochemical of tomatoes, with a potent anti-aging effect. The administration of lycopene was shown to protect the liver, brain, kidney and skin of adult mice against oxidative stress through the enhancement of the activities of antioxidant enzymes [113]. Lycopene was also found to rescue the reduced antioxidant capacity by promoting the activities of antioxidases and activating the Nrf2/Heme oxygenase-1 (HO-1) pathway in both D-gal-induced and naturally aged ovaries of chickens, as well as to promote cell proliferation and inhibit apoptosis in both D-gal-induced and naturally aged ovaries. In addition, lycopene could alleviate D-gal-induced mitochondrial damage in living granulosa cells [114].
Crocin is a natural carotenoid antioxidant obtained from the stigma of saffron flowers [128]. It has recently been reported that crocin possesses anti-aging properties. Middle-aged rats fed with diets containing crocin displayed a relative decline in body weight gain and a reduction in age-associated serum triglyceride levels. Notably, both age-associated macromolecular damage and a decline in endogenous antioxidants as well as an increase in intracellular calcium concentration in the cerebral cortex were all reversed due to the oral administration of crocin. Crocin also improved acetylcholine content and enhanced mitochondrial function [117].
2.3.2. Xanthophylls
Astaxanthin (ATX), naturally found in krill and the microalgae Haematococcus, belongs to a group of xanthophylls with greater antioxidative activity due to the presence of 2 oxygenated groups on each ring structure [129]. ATX has been shown to possess anti-aging activity in both yeast and nematodes [120,130,131,132]. In D-gal-induced-aging rats, ATX was found to be able to decrease MDA content, enhance antioxidative activity, and reduce oxidative stress, ultimately resulting in the repair of damaged liver, due to its ability to activate the Keap1/Nrf2 pathway and suppress the NF-κB pathway [118]. Similarly, ATX administration decreased the levels of oxidative stress markers, including MDA, nitric oxide (NO) and advanced protein oxidation product (APOP), and increased the activities of antioxidant enzymes SOD and CAT in the brains of young and aged mice, thus contributing to the retardation of aging [119].
Canthaxanthin widely exists in marine animals, algae and a few terrestrial plants. It was found that treatment with canthaxanthin decreased the activity of SA-β-Gal, the levels of ROS and MDA, and the expression of pro-inflammatory factors (IL-6, IL-1β, TNF-α), chemokines (CXCL1) and metalloproteinases (MMP-1) but increased the levels of SOD and GSH and the proliferation of the aging-model liver cells (AML12) stressed by H2O2. An in-vivo study also showed that canthaxanthin could reduce the liver fibrosis area of aged mice, decrease serum ALT and AST levels, and downregulate the expression of TNF-α and IL-1β, exhibiting an anti-aging effect on aged livers [123]. These facts indicate that canthaxanthin exhibits anti-aging activity.
Lutein is a superior antioxidant naturally present in green plants and in the fat of plant-eating animals, egg yolk and the retina. It is known that the exposure of skin to UV radiation (photo-aging) leads to a loss of cell viability, membrane damage, and the deposition of excessive elastotic material. Interestingly, lutein was shown to not only improve the viability and membrane integrity of UV-exposed fibroblasts but also to suppress elastin synthesis by the inhibition of the level of matrix metalloproteinases (MMPs). Thus, lutein has anti-skin-aging activity [124].
2.4. Sterols
Sterols are essential components of the membranes of all eukaryotic organisms, including fungi, plants, invertebrates and vertebrates, and play roles in controlling membrane fluidity and permeability. In some plants, sterols have a specific function in cell proliferation, signal transduction and the modulation of the activity of membrane-bound enzymes [133,134]. Sterols also exhibit a wide range of pharmacological effects, including immunomodulatory, hepatoprotective, anti-cancer, antimicrobial, antifungal, anti-inflammatory, cardiotonic and anti-aging activities [135,136,137]. Here, we describe the anti-aging activities of sterols from natural food sources and their possible anti-aging mechanisms (Table 4).
2.4.1. Phytosterols
Plant sterols and their saturated derivatives are called phytosterols. The human body cannot synthesize phytosterols, and we must obtain from the diet [148]. More than 250 phytosterols have already been isolated from dietary and medicinal plants [149]. They are divided into sterols and stanols, representing the unsaturated and saturated molecules, respectively [150]. Stigmasterol, β-sitosterol, campesterol, guggulsterone, diosgenin, sarsasapogenin, physalin A and dioscin are the most common phytosterols found in the diet, including in vegetable oils, whole grains, nuts, fruits, and vegetables [151,152]. Vegetable oils and their products are the richest natural sources of plant sterols [153].
The anti-aging activity of phytosterols has attracted much attention in recent years. It was shown that the phytosterols from the seeds of the dodder Cuscuta chinensis decreased ROS levels, increased heat-stress resistance, and extended the lifespan of aged C. elegans [153]. Our study demonstrated that diosgenin (DG), a naturally occurring steroidal sapogenin found predominantly in the roots of yam Dioscorea villosa and the seeds of fenugreek Trigonella foenum-graecum, exhibited conspicuous anti-aging activity. We clearly showed that DG remarkably extended both the mean and maximum lifespans of the aged male N. guentheri. DG administration also significantly reduced the accumulation of histological aging biomarkers, LF and SA-β-Gal, and decreased the levels of ROS, protein oxidation and lipid peroxidation in aged fish [138]. β-Sitosterol, abundant in nuts, legumes and olive oil, was able to prevent H2O2-treated human dermal fibroblast (HDF) and human permanent epidermal (HaCaT) cells from death, and to exert anti-skin-aging activity by the promotion of the biosynthesis of hyaluronic acid (HA) and the enhancement of skin barrier function [139]. Daucosterol palmitate (DSP), a plant steroid from the herb Alpinia oxyphylla, could ameliorate Aβ-induced learning and memory impairments and inhibit ROS production in a male Alzheimer’s disease rat model [140].
2.4.2. Animal Sterols
Animal sterols contain cholesterol, vitamin D and steroid hormones. Cholesterol, the main animal sterol, acts as a precursor for the synthesis of steroid hormones, vitamin D, bile acids and oxysterols [154]. Vitamin D has two forms: D3 (cholecalciferol) and D2 (ergocalciferol). Animal sterols are present in many animal-derived products, including the flesh of fish, fish oils, egg yolk, beef liver, chicken liver and veal steak [155].
Vitamin D3 is well known for its activities in maintaining and regulating calcium and phosphorus homeostasis and in modulating both male and female reproductive processes [156,157]. The production of vitamin D declines with age in male rodents, leading to the reduction of sperm count, motility and mating ability. This age-associated decline in vitamin D3 level suggests a connection between vitamin D3 and aging [158]. Actually, previous studies have already shown that vitamin D3 was able to improve the aged-associated impaired spermatogenesis of D-gal-induced-aging rats [143] and to alleviate H2O2-induced DNA damage [144]. In addition, it was found that the sterol compounds isolated from the mussel Mytilidae, including cholesterol (CHOL), brassicasterol, crinosterol and 24-methylenecholesterol, could all expand the lifespan of yeast, exhibiting apparent anti-aging activity [145].
2.4.3. Fungal Sterols
Fungi are rich in bioactive compounds, including sterols. Fungal sterols are widely distributed in edible mushrooms [146,159], Chinese cordyceps [147] and yeast [160]. The main type of fungal sterols are ergosterols, which can be used for the synthesis of vitamin D and steroid hormones in animals. Ergosterols are also widely applied in pharmaceuticals, advanced biofuels and perfume ingredients [159].
Several studies have shown that fungal sterols have anti-aging activity. It was shown that ergosterol derivatives, ganodermasides A and B, isolated from the spores of the glossy Ganoderma Ganoderma lucidum, extended the replicative lifespan of the yeast Saccharomyces cerevisiae [146]. Cerevisterol, another sterol isolated from Chinese cordyceps, not only improved the survival rate of H9C2 cells under hypoxia but also exhibited anti-aging effects in mice [147].
2.5. Terpenoids
Terpenoids, composed of five carbon isoprene units, are a large class of natural products that includes more than 40,000 structures widely used in the flavor, fragrance, chemical and pharmaceutical industries [161]. Based on their structures, terpenoids are divided into eight subclasses: hemiterpenoids, monoterpenoids, sesquiterpenoids, diterpenoids, sesterterpenoids, triterpenoids, tetraterpenoids and polyterpenoids [162]. Previous studies have shown that terpenoids have multiple biological effects, including anti-cancer, antioxidant, anti-inflammatory, antibacterial, neuroprotective, anti-diabetic and anti-aging activities [163,164,165,166,167,168,169]. Now, we will describe the anti-aging activity of several representative terpenoids from natural food sources. Table 5 lists the representative terpenoids with possible anti-aging mechanisms, and Figure 2 shows the chemical structures of the different types of terpenoids.
2.5.1. Hemiterpenoids
The hemiterpene compound 3,3-dimethylallyl alcohol (prenol) is an unsaturated prenyl alcohol and one of the simplest members of the terpenoid family. It is present in citrus fruits like lemon, orange and pomelo, where it serves as an aroma constituent and acts as a key precursor of several biological molecules [198]. Prenol has recently been reported to possess anti-aging potential. Prenol supplementation was found to extend the lifespan of wild-type C. elegans up to 22.8% compared to control worms [170]. Moreover, suspended amyloid-β-induced paralysis and reduced α-synuclein aggregation were observed in prenol-treated worms. This lifespan-prolonging property of prenol appeared to be correlated with ameliorated physiological parameters and increased stress (heat and oxidative) tolerance in the nematodes. Both in-silico and gene-specific mutant studies revealed that the longevity transcription factors DAF-16, HSF-1, and SKN-1 were involved in the improved lifespan and health span of prenol-treated worms.
2.5.2. Monoterpenoids
Cuminaldehyde, an aromatic monoterpenoid volatile compound, is an aromatic oily aldehyde found in essential oils obtained from the cumin Cuminum cyminum [171]. Cuminaldehyde was shown to be able to upregulate the expression of Bdnf, Icam and ApoE but downregulate the expression of IL-6 in the brains of aged rats, suggesting that cuminaldehyde has a neuroprotective effect [171]. Asperuloside is the main bioactive compound of iridoid, belonging to monoterpenoid extracted from the Chinese herb Du Zhong Eucommia ulmoides male flower. It was reported that asperuloside could delay the muscle aging of C. elegans through a DAF-16-mediated improvement in mitochondrial dysfunction [172]. Limonene is a naturally occurring cyclic monoterpene, available in a variety of fruits and vegetables, such as citrus and conifer plants. Limonene was able to protect HaCaT cells (human skin keratinocytes) against UVB-induced photodamage and photo-aging through the activation of the Nrf2-dependent antioxidant defense system [173]. Carvacrol (CAR) is a phenolic monoterpenoid present in the essential oils of the oregano Origanum vulgare, the thyme Thymus vulgaris, the pepperwort Lepidium flavum and the wild bergamot Citrus aurantium bergamia [199]. CAR was found to decrease the content of MDA and the relative mRNA expression of p53, p21 and B-cell lymphoma-2 associated X protein (Bax); to increase the activity of total antioxidant capacity (TAC) and GPX; and to upregulate the level of glutathione S-transferase (GST) in the brains of D-gal-induced aged rats. CAR was thus considered a promising natural protective compound capable of delaying aging and maintaining health [174].
2.5.3. Sesquiterpenoids
Dihydro-β-agarofuran-type sesquiterpenoids are the primary secondary metabolites in the seeds of the medicinal plant genus Celastrus [175,200]. Twelve dihydro-β-agarofuran-type sesquiterpenoids have been purified from the seeds of Celastrus virens, and compounds 1, 2, 5, 6, 8, and 9 (at 50 μM) were found to extend the mean survival time of C. elegans. It was further revealed that the extension of lifespan mediated by compounds 1, 6, 8, and 9 was dependent on the transcription factors skn-1 and hsf-1 [175]. Both α- and β-santalol are the most abundant sesquiterpenoids found in the sandalwood Santalum paniculatum. Treatment with α- and β-santalol was shown to retard aging, improve health span, and inhibit the aggregation of toxic amyloid-β (Aβ1−42) and polyglutamine repeats (Q35, Q40, and HtnQ150) in a C. elegans models for Alzheimer’s and Huntington’s disease, respectively. Moreover, α- and β-santalol selectively regulated the transcription factors SKN-1/Nrf2 and EOR-1/promyelocytic leukemia zinc finger (PLZF) through the receptor tyrosine kinase/Ras GTPase/MAP kinase (RTK/Ras/MAPK)-dependent signaling axis capable of triggering the expression of several antioxidant genes and protein aggregation inhibitory genes, such as gst-4, gcs-1, gst-10, gsr-1, hsp-4, and skr-5, which contribute to extending longevity and helping minimize age-induced protein oxidation and aggregation [176]. Patchouli alcohol (PA), a kind of sesquiterpene extracted from the patchouli Pogostemon cablin, was also shown to produce an anti-aging effect. PA could inhibit D-gal-induced oxidative stress and ameliorate the quality of aging cartilage via the activation of the Nrf2/HO-1 pathway in mice [177].
2.5.4. Diterpenoids
Erinacine A (EA) is a diterpenoid derivative extracted from the mycelium of the mushroom Hericium erinaceus (HEM). EA has been reported to reverse spatial learning disabilities in aging mice. It was demonstrated that both HEM- and EA-treated mice had shorter mean daily escape latencies than control group mice. HEM- and EA-treated mice also showed a decrease in the expression of TNF-α and IL-1β. Moreover, HEM and EA could reduce body weight, abdominal fat, plasma glucose, serum and liver total cholesterol and liver triacylglycerol. Thus, HEM and EA may be potential health-promoting supplements for minimizing the progression of aging and obesity-induced neurodegeneration by decreasing metabolic abnormalities and neuroinflammatory cytokines and increasing neurogenesis factors [178]. Carnosol, a phenolic diterpene, is one of the main constituents of the aromatic herb Rosmarinus. Carnosol was able to increase the health span of C. elegans. It effectively decreased ROS accumulation under normal or oxidative stress conditions, significantly increased the activity of CAT, SOD and GPX, and reduced MDA content. Moreover, carnosol-mediated longevity required the upregulated expression of sod-3, sod-5, hsf-1, hsp-16.1, and hsp-16.2, and was dependent on hsf-1 gene. This suggests that carnosol can be used as a potential dietary supplement to slow down aging [179]. Andrographolide (ANDRO) is a diterpenoid lactone, which is the main active constituent of the Chinese traditional herb Chuan Xin Lian Andrographis paniculata. ANDRO administration could increase the recognition memory and preference for novel experiences, restore social recognition and long-term memory, and enhance basal synaptic activity and long-term potentiation (LTP) in aged female degus (a long-lived rodent) Octodon degus. Moreover, ANDRO increased the level of N-methyl D-aspartate receptor subtype 2B (NR2B) in both adult and aged degus, and the level of post-synaptic density protein-95 (PSD95) and Homer1 (homer scaffolding protein 1) in aged degus. Thus, the long-term administration of ANDRO is able to improve age-dependent behavioral and synaptic dysfunction impairment in long-lived female degus [180].
2.5.5. Triterpenes
Compound K (CK) is a secondary ginsenoside biotransformed from major ginsenosides of the herb Panax ginseng, which is more bioavailable and soluble than its parent ginsenosides. Ginsenoside CK was found to improve the memory function in scopolamine-injured mice by regulating Aβ aggregation and promoting the transduction of the Nrf2/Keap1 signaling pathway, thereby resulting in a reduction in oxidative damage to neurons and the inhibition of neuronal apoptosis [181]. Similarly, CK treatment attenuated chronic cerebral hypoperfusion (CCH)-induced Aβ1–42 deposition and ameliorated cognition impairment in vascular-dementia rats by upregulating the expression of both pSer9-glycogen synthase kinase 3β (pSer9-GSK3β) and insulin-degrading enzyme (IDE), which are responsible for the production and clearance of Aβ1–42 [182]. This suggests that CK may serve as a potential agent for the prevention and treatment of aging-induced Alzheimer’s disease. In addition, CK supplementation could diminish the production of COX-2 and metalloproteinase-1 (MMP-1) in NIH3T3 cells treated with UV-B and modulate the expression of type I collagen [183]. Rg1, another kind of ginsenoside, also possesses anti-aging activity [184,201]. It was found that Rg1 could exert anti-aging functions by suppressing mitochondrial pathway-mediated apoptosis and activating the sirtuin 3 (SIRT3)/SOD2 pathway in Sca-1⁺ HSC/HPC cells in a D-gal-induced-aging rat model [184]. Moreover, 20-O-β-D-glucopyranosyl20(S)-protopanaxadiol (20GPPD), the primary bioactive metabolite of ginsenoside Rb1, enhanced the production of hyaluronic acid by acting as an upstream modulator of ERK and Akt activity mediated by Src kinase in human keratinocytes [186].
Ganoderic acid D (GA-D) is a triterpenoid compound produced by the Ganoderma G. lucidum. It was shown that GA-D treatment inhibited the activity of SA-β-Gal, decreased the ROS level and the expression of P21 and P16 proteins, relieved the cell-cycle arrest, and enhanced the telomerase activity in senescent human amniotic mesenchymal stem cells (hAMSCs). Furthermore, GA-D was able to alleviate the senescence of hAMSCs through the activation of the CaM/CaMKII/Nrf2 (Ca2+ calmodulin/CaM-dependent protein kinase II/nuclear erythroid 2-related factor 2) signal pathway [187,188]. Maslinic acid (MA) is a triterpene derivative obtained from the olive tree Olea europaea. MA showed antioxidant activity and was capable of reducing the endogenous plasma lipoperoxide levels and susceptibility to lipid peroxidation in rats, thus offering some advantages in the anti-aging process [189]. Ursolic acid (UA) is a natural triterpenoid compound extensively present in apple peels. UA was found to promote skeletal muscle rejuvenation by enhancing SIRT1 expression and satellite cell proliferation [190,202]. Moreover, UA treatment also reversed the aging of the liver by enhancing SIRT1 and SIRT6 levels and promoting the production of PGC-1β (peroxisome proliferator-activated receptor γ coactivator 1) and Klotho [191]. Cycloastragenol (CA) is a natural triterpenoid saponin compound obtained from the milkvetch root Astragali radix. Both CA and its new derivatives could significantly extend the lifespan of C. elegans [192].
2.6. Vitamins
Vitamins are a structurally dissimilar group of organic compounds that share the common features of being essential for normal cellular functions, growth and development. Most vitamins cannot be produced in human body, and they must be obtained through dietary intake. Vitamins are divided into two groups: water-soluble vitamins and fat-soluble vitamins. The former are soluble in water and polar solvents and mainly consist of B vitamins and vitamin C, and the latter are insoluble in water but soluble in fat and organic solvents and comprise vitamins A, D, E and K [203]. Previous studies have shown that vitamins have multiple biological effects, including antioxidant, anti-aging, anti-inflammatory, anti-nociceptive and anti-cancer properties [204,205]. Here, we describe the anti-aging activities of water-soluble vitamins and fat-soluble vitamins from natural food sources and their possible anti-aging mechanisms (Table 6).
2.6.1. Water-Soluble Vitamins
B vitamins include vitamins B1 (thiamin), B2 (riboflavin), B3 (nicotinic acid/niacinamide), B5 (pantothenic acid), B6 (pyridoxine), B7 (biotin), B9 (folate) and B12 (cobalamin), which are grouped together due to their water solubility, though they are a diverse group of molecules with varied metabolic functions related to energy production, protein metabolism and hemopoiesis [215]. Chemically, riboflavin (RF) is 7, 8-dimethyl-10-ribityl-isoalloxazine and consists of a flavin isoalloxazine ring bound to a sugar side chain, ribitol [216]. RF, or vitamin B2, is heat-stable. Cooking does not lower levels of RF; however, exposure to light could destroy it. RF can be found in a wide variety of foods and from natural sources, especially in milk and organ meats—mostly in calf liver, egg, fish, nuts, certain fruits and legumes, wild rice, mushrooms, dark green leafy vegetables, yeast, beer, cheese and dietary products [217,218]. Previous studies have demonstrated that RF has anti-aging effects. For example, the supplementation of RF was shown to significantly extend the lifetime and strengthen the reproduction of fruit flies by enhancing the activity of antioxidant enzymes [206]. PVN, a topical liquid formula of polydeoxyribonucleotide (PDRN), vitamin C, and niacinamide (a kind of vitamin B3 derivant), was shown to be capable of resisting UV-B-induced skin aging. PVN treatment increased the expression of Nrf2/HO-1 and the activity of SOD and decreased the activities of nicotinamide adenine dinucleotide phosphate hydrogen oxidase and tyrosinase, as well as the expression of tumor protein p53 and microphthalmia-associated transcription factor, in UV-B-radiated animal skin. PVN also decreases melanin content in the skin. Moreover, PVN treatment decreased the expression of the nuclear factor kappa-light-chain enhancer of activated B cells and MMP2/3/9 but increased the expression of the collagen type I α1 chain [207].
Vitamin C, or ascorbic acid, is an essential dietary nutrient and one of the naturally occurring antioxidants in nature [219,220]. It has been shown that vitamin C is capable of repairing DNA, alleviating oxidative stress, and modulating the activity of telomeres in the aging process, thereby eventually leading to longevity [221]. Vitamin C was generally used as a supplement in cosmetic and dermatologic products for anti-skin-aging purposes [208,222,223,224]. For instance, a split-face, randomized controlled trial indicated that vitamins C and E improved skin color, elasticity, radiance, smoothness, scaliness, and wrinkles of fifty female volunteers aged 30–65 years [225]. Additionally, it was reported that vitamin C delayed liver aging by reducing lipid deposition [209]. Vitamin C administration also decreased the expression of fatty acid synthase (FAS), acetyl-CoA carboxylase (ACC), and ATP-citrate lyase (ACL), and reduced the contents of total cholesterol ratio (TC), triglycerides (TGs) and non-esterified fatty acids (NEFAs) through the regulation of GSK-3β/mTOR signaling in the liver of zebrafish treated with LiCl [209].
2.6.2. Fat-Soluble Vitamins
Retinol is the bioavailable form of vitamin A and has been reported to possess the ability to reduce skin discoloration, stimulate collagen production, reduce rhytids, and improve acne and uneven skin texture, thus exhibiting anti-skin-aging activity [226,227]. Recently, retinol has also been shown to exert anti-skin-aging activity by decreasing glycan metabolism, enhancing protein synthesis/folding, and being involved in cytoskeletal rearrangement [228].
Vitamin E includes eight structurally related lipid-soluble compounds with potent antioxidant properties, consisting of four tocopherols and four tocotrienols: α (alpha), β (beta), γ (gamma) and δ (delta) [229]. α-Tocopherol is the most abundant and bioavailable form of vitamin E in humans and rodents [230,231] and serves as a strong ROS scavenger that protects polyunsaturated fatty acids in cellular membranes and lipoproteins from peroxidation [232]. In a DNA repair-deficient mutant mouse (Xpg−/−), vitamin E supplementation exhibited an obvious neuroprotective effect. Vitamin E resulted in a delayed onset of age-related body weight decline and the appearance of tremors and considerably prevented DNA damage-induced liver abnormalities such as changes in polyploidy. Additionally, the intake of vitamin E reduced the number of p53-positive cells throughout the brain, indicative of a lower number of cells dying due to DNA damage accumulated over time [210]. A previous study also reported that vitamin E, or velvet antler polypeptide, could significantly improve the learning and cognitive abilities of D-gal-induced-aging mice, increase the activities of SOD, GPX, and CAT in the serum, and decrease the MDA content. Intestinal microecological analysis showed that vitamin E, or velvet antler polypeptide, markedly increased the abundance of the beneficial bacterial genus Lactobacillus. Metabolism analysis showed that vitamin E, or velvet antler polypeptide, promoted fatty acid metabolism by activating peroxisome proliferator-activated receptor α (PPARα) and upregulating the expression of the downstream enzymes carnitinepalmitoyl transferase-1 A and acyl-CoA oxidase 1 while downregulating that of apolipoprotein E4 (APOE4). Thus, vitamin E, or velvet antler polypeptide, is able to exert anti-aging activity through the modulation of the gut microbiota and the regulation of the PPARα/APOE4 pathway [211]. Similarly, dietary quercetin and vitamin E were also shown to improve intestinal function in aged breeder hens by protecting intestinal structure and integrity [212]. Quercetin and vitamin E exerted synergistic effects on intestinal morphology by promoting villi height and crypt depth, mitigating the intestinal inflammatory damage of the aged hens, decreasing the concentration of serum D-lactate and diamine oxidase, and increasing the levels of secretory immunoglobulin A and Mucin-2 mRNA. Furthermore, the expression of intestinal tight junction protein genes including occludin, ZO1, and claudin-1 was increased by quercetin and vitamin E. Quercetin and vitamin E could also lower the expression of the pro-inflammatory genes (TNF-α, IL-6, and IL-1β) and increase the expression of anti-inflammatory genes (IL-10 and IL-4). Moreover, quercetin and vitamin E protected the small intestinal tract from oxidative damage by increasing the levels of SOD, GPX, and CAT and the expression of SOD1 and GPX-2, and decreased MDA levels in the intestine [212]. Vitamin E was also reported to be able to prevent age-related neuronal disorders by suppressing oxidative stress and enhancing antioxidant enzyme activity [233,234], protecting the integrity of the skin barrier, thus possessing anti-skin-aging activity [235,236,237].
Vitamin K is another kind of fat-soluble vitamin with a common chemical structure: a 2-methyl-1,4-naphthoquinone ring and a variable aliphatic side chain. The variable aliphatic chain differentiates two isoforms: vitamin K1, or phylloquinone, and vitamin K2, usually designated as menaquinone. Vitamin K is abundant in dark green leafy vegetables, several fruits (e.g., dried prunes, kiwifruit, avocado, blueberries, blackberries, grapes), some nuts (pine nuts, cashews, pistachios), cheeses, eggs, and meats [238]. Previous studies demonstrated that vitamin K is a vital cofactor in activating several proteins that act against aging and age-related diseases [239,240]. Thus, vitamin K status is closely associated with aging and age-related diseases [241,242,243]. Vitamin K was initially discovered as a co-factor for γ-glutamyl carboxylase (GGCX), which could add a carboxyl group to the gamma-position carbon of glutamate residues in the substrate proteins [244,245]. A recent study demonstrated that vitamin K could alleviate aging-related musculoskeletal disorders such as osteoporosis, osteoarthritis, and sarcopenia by enhancing GGCX activity [246]. Meanwhile, other modes of vitamin K actions, such as the regulation of transcription by activating steroid and xenobiotic receptor (SXR), physical association to 17β-hydroxysteroid dehydrogenase type 4 (17β-HSD4), covalent modification of Bcl-2 antagonist killer 1 (Bak) and modulation of protein kinase A (PKA) activity, were also reported [246]. Vitamin K could improve aging and aging-related diseases through its antioxidant properties. Treatment with vitamin K was shown to decrease ROS and lipid peroxidation levels, increase the glutathione (GSH) level and the activities of both GPX and alkaline phosphatase (ALP), and promote DNA proliferation in human osteoblasts cultured in the presence of hydroxyapatite-based biomaterials that cause oxidative stress [213]. A 4-week randomized controlled trial in middle-aged and older individuals indicated that dietary intake of vitamin K-rich green leafy vegetables decreased the fracture risk of individuals by substantially reducing serum total osteoblasts, osteocalcin (OC) and undercarboxylated OC, which suggests the increased entry of OC into the bone matrix, where it may improve the material properties of bones [247]. An increase in the intake of dietary vitamin K was associated with better cognitive function scores in an older adult Mediterranean population with high cardiovascular risk [248] and in adults with chronic kidney disease [249]. Recently, vitamin K2 was reported to extend the lifespan of C. elegans and improve the resistance to pathogenic infection, heat stress and H2O2-induced inner oxidative stress [214]. Interestingly, the roles of vitamin K2 on aging and stress resistance were shown to be dependent on enhanced fat metabolism but not due to its antioxidant effects, suggesting that vitamin K2 could enhance fat degradation and digestion to improve survival, supporting the effectiveness of vitamin K2-based medical treatments [214].
3. Anti-Aging Mechanisms of Compounds from Food Sources
We have provided a brief introduction to compounds from natural food sources, including polysaccharides, polyphenols, carotenoids, sterols, terpenoids and vitamins above. They have been shown to display anti-aging effects in different organism models, including yeast, nematode, fruit flies, fish, hens and mice. Now, we will discuss their modes of anti-aging action. Currently, the anti-aging mechanisms of the compounds are mainly found to be associated with several modes of action, such as improved antioxidant capacity, regulation of age-related gene expression, improved immune function, regulation of apoptosis, intestinal flora regulation, regulation of autophagy and suppression of cellular senescence.
3.1. Suppression of Oxidative Stress
All animals produce ROS during normal physiological activity, especially in the course of oxidative phosphorylation. At the same time, ROS-scavenging systems including the antioxidant enzymes CAT, SOD and GPX also run in parallel in the body. However, the balance between the ROS and ROS-scavenging systems is becoming increasingly difficult to maintain with increased age, resulting in an excess of ROS. Excess ROS can cause the peroxidation of lipids, the oxidation of proteins, and DNA and mitochondria damage, thereby impairing cellular integrity and functionality, ultimately leading to the deteriorated health status of an organism and accelerating aging [250]. The Keap1/Nrf2/AREs (Kelch-like ECH-associated protein 1/nuclear factor erythroid 2-related factor 2/antioxidant-response elements) signaling pathway is a defensive transduction system for animals to regulate oxidative stress. Keap1 is an inhibitor of Nrf2. Normally, Nrf2 is bound to Keap1 and remains inactive in cytoplasm [251]. When stimulated by internal and external free radicals or chemicals, the conformation of Keap1-Nrf2 changes and Nrf2 dissociates from Keap1 and translocates into the nucleus and interacts with the AREs, eventually activating a series of antioxidant genes such as heme oxygenase-1 (HO-1), nicotinamide adenine dinucleotide phosphate (NADPH), GST, SOD, and GPX [252,253].
It is known that polysaccharides, polyphenols, carotenoids, sterols, terpenoids and vitamins can all have anti-aging effects through the suppression of oxidative stress. Polysaccharides, including LBP, CPs (polysaccharides of the dangshen Codonopsis pilosula), SCPs (sulfated polysaccharides of C. pilosula) and SFPs (polysaccharides of the hijiki Sargassum fusiforme), were all able to exert anti-aging activity through the activation of the Keap1/Nrf2/ARE pathway, which enhances antioxidant system activity, ultimately resulting in the scavenging of ROS, a reduction in DNA damage, and the protection of lipids and proteins from oxidation [34,40,49,50]. Polyphenols such as quercetin, rutin, anthocyanin, resveratrol, flavonoid and phenolic acids also exhibited antioxidant activity by regulating the production and activity of endogenous antioxidant enzymes SOD, GPX, GSH, NADP(H) quinone oxidoreductase 1 (NQO1), GST, and HO-1, which involves the Keap1/Nrf2/AREs-mediated pathway [79,80,254,255]. Carotenoids like lutein were shown to protect cells from H2O2-induced senescence by promoting the expression of antioxidant effectors such as NADPH quinone dehydrogenase 1, HO-1 and sirtuins [125]. Interestingly, astaxanthin (ATX) exerted anti-aging effects through the regulation of both antioxidative activity and anti-immunosenescence activity, which are mediated by Keap1/Nrf2 and NF-κB pathways, respectively [118]. The sterol vitamin D3 was found to improve age-associated spermatogenesis impairment through the regulation of antioxidant system activity via enhancing SOD, GSH and CAT activity [143], and treatment with vitamin K and D3 decreased the ROS and lipid peroxidation levels and increased the glutathione (GSH) level and the activity of GPX in the presence of hydroxyapatite-based biomaterials that cause oxidative stress [213]. Notably, we found that DG extended both the mean and maximum lifespans of the aged male fish N. guentheri through the enhancement of the activity of antioxidant enzymes, including CAT, SOD and GPX; the promotion of the proteolytic activity of the ubiquitin–proteasome pathway; and the suppression of the phosphatidylinositol 3-kinase/protein kinase/molecular target of the rapamycin (PI3K/AKT/mTOR) signaling pathway [138]. The monoterpenoid limonene and terpenoid platycodin D both suppressed intracellular ROS generation by increasing the production of endogenous antioxidant enzymes [173,194], which are associated with enhanced Nrf2. Similarly, the terpenoid ginsenoside Re (GRe) attenuated increased NADPH oxidase (NOX) activity and ROS levels, increased GPX activity, and improved cognitive dysfunction in Klotho-deficiency-induced-aging mice via the upregulation of Nrf2/GPX signaling [195].
3.2. Regulation of Age-Related Genes and Pathways
Quite a few genes, including those coding for Sirtuin1 (SIRT1), cellular tumor antigen p53 (p53), cyclin-dependent kinase inhibitor 1 (p21) and the 66-kDa isoform of ShcA (p66Shc), and several pathways, such as the IIS pathway and the rat sarcoma/protein kinase A (Ras/PKA) pathway, have been identified as related to aging and longevity. Mutations and/or changes in the expression of the genes and pathways can significantly impact the lifespan of organisms.
SIRT1 is a member of the sirtuins (SIRTs) family, which plays a protective role in the development of many age-related diseases, including cardiovascular disease, neurodegeneration and cancer [256,257]. Previous studies have shown that the expression of SIRT1 leads to an increase in the DNA stability and survival rate of animals [258]. SIRT1 has been found to regulate many biological processes, including cellular senescence, apoptosis, glucose homeostasis, aging and longevity. The protein p53, a short-lived tumor suppressor, is normally ubiquitinated rapidly by mouse double minute 2 protein (MDM2), a p53-specific E3 ubiquitin ligase, and subsequently targeted for degradation by the ubiquitin–proteasome system. In contrast, in the presence of DNA damage, p53 is activated by post-translational modifications, which inhibit the interaction of p53 with MDM2 and lead to the stabilization and accumulation of p53. As p53 not only triggers apoptosis but also induces DNA damage, the expression of the p53 gene is thus related to both cell senescence and cell-cycle arrest, thereby exerting an influence on aging [259]. The cell-cycle inhibitor p21 (CDKN1A) is involved in many important cellular processes, including apoptosis and DNA replication. CDKN1A is also a cell-cycle regulatory protein capable of inhibiting the activities of various cell-cycle-dependent kinases, ultimately resulting in cell-cycle arrest [260]. Polysaccharides have been reported to affect the aging process by interfering with the cell cycle via the regulation of the expression of both SIRT1 and p53 as well as the CDKN1A genes. For example, the polysaccharide extracted from the root of Yulangsan Millettia pulchra Kurz (YLSP) was able to reduce the expression of p53 and p21 genes in D-gal-induced mice, which is responsible for the delay of liver and brain senescence [41]. Tremella fuciformis polysaccharides (TFPs) could attenuate hydrogen peroxide (H2O2)-induced cell oxidative stress and apoptosis through the upregulation of the SIRT1 pathway [60], and LBP alleviated cell apoptosis and aging through the p53-mediated pathway [36]. Similarly, β-carotene reduced aging rates in tissues and organs in vivo and appeared to inhibit aging caused by antioxidative stress by regulating KAT7-P15 signaling [112], and the polyphenol resveratrol protected the impairment of learning and memory ability and suppressed neuronal apoptosis in aged rats induced by sevoflurane and nitrous oxide through upregulating the expression of Sirt1 [87]. Interestingly, the water-soluble vitamin B3 derivant niacinamide also exhibited a protective effect against UV-light-induced DNA damage and aging in epidermal melanocytes by increasing the components of various signaling pathways, such as Sirt1 and Nrf2 [261].
p66Shc, a growth factor adapter protein, has been shown to affect ROS production by reducing ROS scavenging, by increasing membrane oxidase activity, or through mitochondrial respiratory chain leakage. It can also suppress the expression of antioxidant genes by inhibiting Forkhead box O 3a (FoxO3a) activity [262,263,264]. Our previous study demonstrated that β-1,3-glucans administration increased the activities of antioxidant enzymes, including CAT, GPX, and SOD, by decreasing the level of p66Shc. This resulted in the reduction of ROS levels, which in turn slows down protein oxidation, lipid peroxidation, LF, and SA-β-Gal development, eventually extending the lifespan of aging fish [58]. Similarly, polyphenol caffeic acid (CA) and dihydrocaffeic acid (DHCA) promoted longevity and increased stress resistance in C. elegans by activating the DAF-16/FoxO transcription factor and modulating the expression of stress-related genes [76], and the sterol β-sitosterol attenuated aging sarcopenia via regulating FoxO1-dependent signaling in a mouse model [141]. Notably, the terpenoid ginsenoside Rg1 exerted anti-aging effects by suppressing mitochondrial pathway-mediated apoptosis and the SIRT3/SOD2 pathway in Sca-1⁺ HSC/HPC cells of an aging rat model [184].
The IIS pathway is closely associated with the aging and longevity of animals. Normally, IIS is active and is mainly involved in the phosphorylation of DAF-2, AGE-1 and other kinases, thus affecting the activity of DAF-16 [265], a transcription factor mediating the aging rate of animals like C. elegans [266]. Any condition that causes internal stress to block the IIS pathway will induce DAF-16 to enter the nucleus; in the nucleus, DAF-16 binds to the promoters and regulates the transcription of its target genes, which are predominantly stress-resistant genes and longevity-promoting genes such as sod-3, skn-1, sir-2.1 and hsp-16.2, thereby delaying senescence and prolonging the lifespan of animals [267,268]. Several studies demonstrated that polysaccharides prolonged the lifespan of C. elegans and D. melanogaster through the regulation of the IIS/FoxO signal pathway [32,39,45,47,269].
The Ras/PKA pathway regulates several aspects of cellular physiology, including growth and responses to glucose and stress, through the phosphorylation of different transcription factors that are also mediated by other signaling pathways [270]. The hexose transporter 7 gene, hxt7, can be used as a reporter of Ras/PKA activity, and the expression of hxt7 is repressed when the Ras/PKA pathway is active [271]. In addition, the Ras/PKA pathway also mediates redox response through the downregulation of the expression of cytoplasmic catalase T (CTT1) and mitochondrial SOD2. It has been demonstrated that both GFGs and HEGs exert anti-aging and neuroprotective effects through the inhibition of the Ras/PKA pathway [52]. Polysaccharides can also affect the lifespan and aging of animals by regulating other lifespan-related signaling pathways. For example, LBP was shown to exert its anti-aging activity by activating MAPK and inhibiting the TOR/S6K (target of rapamycin/ribosomal s6 protein kinase) signaling pathway [31]. Similarly, tart cherry extract (TCE, the main component of anthocyanins) significantly increased the lifespan of C. elegans through the alteration of the AMPK/AMP-activated protein kinase (AAK-2) and DAF-16/IIS pathways [82], and the terpenoids prenol and dihydro-β-agarofuran-type sesquiterpenoid both extended the lifespan of C. elegans through the downstream transcription factors of the IIS pathway, HSF-1 and SKN-1 [170,175].
3.3. Immune Modulation
Aging impairs immunity, resulting in overall dysfunctions. This has been termed immunosenescence, manifested by age-related defects in both humoral and cell-mediated immune responses [272]. Meanwhile, senescent cells usually produce excessive inflammatory cytokines such as IL-1β, interleukin-1 (IL1), TNF-α, and chemokines like C-X-C motif ligand 1 (CXCL1), leading to serious inflammatory responses [273]. Many studies have demonstrated that polysaccharides exert anti-aging activity by enhancing immunity function while suppressing inflammatory response [41,274]. LBP was shown to alleviate the neuroinflammation of estrogen deficiency-induced-aging mice through the downregulation of IL-6, IL-1β and TNF-α levels by inhibiting the toll-like receptor 4/nuclear factor-kappa B (TLR4/NF-κB) signaling pathway [33], and RGBPs were found to attenuate skin aging caused by UV and atopic dermatitis by increasing antioxidant activity, inhibiting activating protein-1 (AP-1) transactivation, and reducing chemokine MDC/CCL22 and TARC/CCL17 levels [43]. Our previous study demonstrated that β-1,3-glucans exerted anti-aging activity by regulating the immune system via enhancing levels of T helper cells (CD4+) and delayed-type hypersensitivity (DTH) response, a T cell-mediated immune response, as well as promoting the production of total anti-keyhole limpet hemocyanin (KLH) immunoglobulin G (IgG), anti-KLH IgG1 and anti-KLH IgG2a levels in aged mice without disturbing immune homeostasis [59].
Polyphenols, sterols, carotenoids, terpenoids and vitamins also exert an anti-aging effect though improving inflammatory response. The polyphenol resveratrol administration delayed the aging of the fish N. guentheri, reversed the increase in SA-β-Gal activity with aging, downregulated the levels of senescence-associated secretory phenotype (SASP)-associated proinflammatory cytokines IL-8 and TNF-α, and upregulated the expression of anti-inflammatory cytokine IL-10 [88]. In addition, resveratrol exerted anti-aging effects by regulating both humoral and cell-mediated immune responses. It demonstrated that the dietary intake of resveratrol induced a significant increase in CD4+ cells in middle-aged and aged Wistar male rats, increased the DTH response in aged rats, and remarkably promoted the production of total anti- KLH IgG, anti-KLH IgG1, and anti-KLH IgG2a in aged rats without disturbing immune homeostasis [89]. The carotenoid trans-lycopene (from tomato juice) alleviated the risk of aging-associated cardiovascular disease by reducing the concentration of important inflammatory molecules related to atherosclerosis [115], and lycopene showed protective effects in the learning and memory functional deficits of Aβ-induced Alzheimer’s disease rats by reducing the expression of toll-like receptor 4 (TLR4) and NF-κB p65 and the levels of TNF-α, IL-1β, and IL-6β in serum [116]. The sterol β-sitosterol showed an anti-aging effect by preventing TNF-α-induced gonadotropin-releasing hormone (GnRH) decline through the inhibition of NF-κB activation [142]. Krill oil, rich in ATX, exerted its anti-aging and rejuvenation effects via the enhancement of the antioxidant system and the suppression of the NF-κB signaling pathway [122]. The terpenoid Rg1 ameliorated aging-induced liver fibrosis in SAMP8 mice through the inhibition of NADPH oxidase 4/NACHT, LRR, and PYD domain-containing protein 3 (NOX4/NLRP3) inflammasome activation [196]. Similarly, quercetin and vitamin E improved intestinal function in aged breeder hens by protecting the intestinal structure and integrity through the suppression of inflammation and the enhancement of antioxidant activity [212].
3.4. Regulation of Apoptosis
Apoptosis plays an important role in the maintenance of homeostasis when intracellular or extracellular damage occurs. On one hand, non-functional and damaged cells can be scavenged by activated apoptosis, and on the other hand, apoptosis dysregulation, along with aging, contributes to age-related pathologies. Thus, apoptosis is involved in aging and age-related diseases [18,275]. Polyphenols have been shown to affect aging and age-related diseases by regulating apoptosis. For example, quercetin alleviated H2O2-induced vascular smooth muscle cell (VSMC) senescence by regulating apoptosis through P53-P21 and P16 pathways [78], and resveratrol improved the pancreas aging of senescence-accelerated mice (SAM) by modulating the inflammatory, oxidative and apoptotic status related to aging [90].
Carotenoids, sterols and terpenoids also showed anti-aging effects through the regulation of apoptosis. The carotenoid astaxanthin was found to enhance the longevity of Saccharomyces cerevisiae by decreasing oxidative stress and apoptosis [120]. Astaxanthin alleviated glutamate excitotoxicity-related neuronal loss associated with Alzheimer’s disease by regulating oxidative stress and apoptosis through the Akt/glycogen synthase kinase-3b (GSK-3β) signaling pathway [121]. The sterol vitamin D3 delayed the testicular senescence of a D-gal-induced-aging rat model by regulating proliferation and apoptosis [143]. The terpenoid ginsenoside Rg1 ameliorated spatial learning and memory deficits in D-galactose and AlCl3-induced-aging mice by restoring fibroblast growth factor 2-protein kinase B (FGF2-Akt) and the brain-derived neurotrophic factor-tropomyosin-related kinase B (BDNF-TrkB) signaling axis to inhibit apoptosis [197]. Similarly, ginsenoside GRb1 retarded the aging process in natural-aged C57BL/6J mice by regulating the cell cycle and apoptotic pathway, which were associated with the alleviation of metabolic disorders [185]. Moreover, the monoterpenoid carvacrol (CAR) delayed the aging rates of D-gal-induced-aging rats by decreasing the expression of P53, P21 and Bax, leading to the inhibition of apoptosis [174].
3.5. Intestinal Flora Regulation
The gut microbiota of animals shows a wide inter-individual variation, but its within-individual variation is relatively stable over time. With the advance of chronological age, the overall richness of gut microbiota in animals decreases, while a certain group of bacteria associated with frailty increases. Studies using model animals have shown that age-related gut dysbacteriosis, or dysbiosis for short, is contributable to unhealthy aging and reduced longevity [276]. It has been reported that the risk of cognitive decline and neurodegenerative diseases caused by aging can be reduced through the regulation of the gut microbiota and metabolites. For example, an increase in the abundance of Faecalibacterium prausnitzii, Eubacterium and Roseburia, induced by the Mediterranean diet, was positively associated with several markers of improved cognitive function [277,278]. Polysaccharides can be entirely fermented by the intestinal microbiota and increase the number of probiotic bacteria, ultimately benefiting healthy aging. WMPs were reported to significantly improve the locomotor activity and spatial and recognition memory of aging mice by both alleviating oxidative stress and decreasing pro-inflammatory cytokine levels, as well as increasing the short-chain fatty acid (SCFA) level and abundance of the beneficial bacteria Bacteroides and Parabacteroides [55]. FLAPs and FHSPs were demonstrated to prolong the lifespan of C. elegans by improving the antioxidant defense system and enriching specific gut bacteria (Romboutsia and Weissella) and metabolites [51]. Similarly, GRPs were found to extend lifespan and alleviate the aging of C. elegans by increasing antioxidant activity, altering the composition of gut flora, and inducing the preferential synthesis of beneficial fatty acids [38]. Interestingly, vitamin E also exerted anti-aging activity through the modulation of the gut microbiota and regulation of the PPARα/APOE4 pathway [211].
3.6. Autophagy Regulation
Macroautophagy, often simply referred to as autophagy, exists widely in eukaryotic cells and is closely associated with many physiological and pathological processes. In the protein degradation machinery, autophagy is primarily involved in the degradation of long-lived proteins and, as a major cellular self-degradation process, helps remove damaged or excessive proteins and organelles. During autophagy, autophagic vacuoles are fused with lysosomes to generate autolysosomes, and the cellular debris and damaged proteins are then degraded in autolysosomes. Mitophagy, a form of selective autophagy, is a crucial mechanism for controlling mitochondrial quality through the removal of dysfunctional or damaged mitochondria. Both autophagy and mitophagy play a dual role in aging and aging-associated diseases. When they are weakened, they cause aging and aging-related diseases; when they are too strong, they induce the autophagy death of normal cells [279,280].
Bioactive compounds from natural food sources can work as essential autophagy modulators and thus be proficiently used in the control of aging and aging-related diseases, in which autophagy plays a crucial role. In 6-hydroxydopamine (6-HODA)-induced PC12 cells (Parkinson’s disease model cells), the expression of the key regulator of autophagy, LC3-II, was decreased, and this could be reversed by treatment with APS (astragalus polysaccharide) through the PI3K/AKT/mTOR pathway [281]. APS also provided a strong protective effect against hepatocyte senescence and pathological damage in aged mouse livers by reducing ROS levels, inhibiting apoptosis and pyroptosis, and promoting mitophagy via the AMPK/mTOR pathway [282]. It was also found that the Echinacea purpurea polysaccharide could improve oxidative stress-induced liver injury by promoting phosphatase and tensin homolog (PTEN)-induced putative kinase 1 (PINK1)/E3 ubiquitin ligase (Parkin)-dependent mitophagy [282]. The protein levels of LC3-II and Beclin were abundantly expressed in a Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinson’s disease (PD) mice model, suggesting the overactivation of autophagy, but they were significantly downregulated by Lycium barbarum polysaccharide (LBP) treatment [283]. Similarly, pretreatment with LBP also reduced PM2.5-induced mitophagy and mitochondrial damage [35]. The Ganoderma lucidum polysaccharide was also shown to ameliorate MPTP-induced Parkinsonism and protect dopaminergic neurons from oxidative stress via regulating mitochondrial function, autophagy, and apoptosis [284].
Interestingly, green tea polyphenols also protected against early vascular senescence in young high-fat-diet rats by ameliorating oxidative injury and promoting autophagy, which was partially regulated by the SIRT3 pathway [285]. In C. elegans models of PD, chlorogenic acid (CGA), a polyphenolic substance derived from various medicinal plants, showed anti-PD effects through autophagy induction via increasing the expression of autophagy-related genes, including unc-51, bec-1, vps-34, and lgg-1 [286]. Oroxin B (OB), a flavonoid isolated from traditional Chinese herbal medicine, alleviated aging-related osteoarthritis (OA) through anti-inflammation, the inhibition of the PI3K/AKT/mTOR signaling pathway and the enhancement of autophagy [287]. Resveratrol was also shown to suppress age-related sarcopenia and cardiomyocyte hypertrophy through the restoration of autophagy in aged mice via the activation of SIRT1 [288]. Similarly, cucurbitacin B (CuB), containing cerebrosides, phenols, sesquiterpenoid, triterpenoids, and sterols isolated from natural products, was reported to prolong both the replicative lifespan and chronological lifespan in yeast by regulating autophagy, ROS, antioxidative ability, and aging-related gene expression [289].
3.7. Suppression of Cellular Senescence
Cellular senescence refers to an intrinsic aging process in which cells undergo irreversible growth arrest due to their inherent finite lifespan or exposure to stress [11,290]. The number of senescent cells increases exponentially with age in various tissues and organs, playing a critical role in the development and pathogenesis of age-related diseases. Cellular senescence generally acts as an inherent anti-cancer mechanism because senescent cells lose the ability to proliferate and perform apoptosis in response to DNA damage [291]. However, senescent cells remain highly metabolically active and exhibit a hypersecretory state known as the senescence-associated secretory phenotype (SASP). The SASP is mainly composed of proinflammatory cytokines, chemokines, proteases, lipids, growth factors and insoluble proteins or extracellular matrix (ECM) components, which are simultaneously often used as markers to identify cellular senescence accurately [292]. The primary role of the SASP is to recruit immune cells to the site of damage and clear the senescent cells through inflammatory mechanisms. As a result, the SASP molecules work transiently in a beneficial manner to perform immune surveillance, promote tissue repair and homeostasis, and suppress tumorigenesis [292]. A recent study showed that the efficient induction of senescence in DNA-damaged cells avoids a potential sub-population of damaged cells, eventually leading to the extension of lifespan [293]. However, an accumulation of senescent cells with age, or chronic senescence, is accompanied by a high rate of secretion of SASP factors, which frequently exceeds the immune system’s clearance capacity [294]. The improper disposal of senescent cells or overactivation of the SASP can result in detrimental effects and increase the risk of disease and mortality [295].
Accumulating data indicated that bioactive compounds from natural food sources exert anti-aging effects by mediating cellular senescence. Fucoidan, a marine-sulfated polysaccharide, was shown to reverse the p-cresol-induced cellular senescence of mesenchymal stem cells (MSCs) via the regulation of SMP30 and p21 (the senescence-associated proteins) and increase proliferation through the regulation of cell-cycle-associated proteins cyclin-dependent kinase 2 (CDK2), cyclin-dependent kinase 4 (CDK4), cyclin D1, and cyclin E, which are activated through the focal adhesion kinase (FAK)-Akt-class A basic helix-loop-helix protein 38 (TWIST) axis [296]. In the D-gal pre-administrated rats, treatment with the Angelica sinensis polysaccharide (ASP) rescued the senescence of hematopoietic cells and bone marrow stromal cells (BMSCs), reserved myeloid progenitor cells, attenuated stromal oxidative load, ameliorated stem cell factor CXCL12 and granulocyte-macrophage colony-stimulating factor (GM-CSF) production, and increased connexin-43 (Cx43) expression. A further study indicated that ASP ameliorated D-gal-induced senescence by inhibiting the secretion of IL-1, IL-6, TNF-α, and the chemokine RANTES, enhancing Cx43-mediated intercellular communication, and improving runt-related transcription factor 2 (Runx2) expression, while decreasing peroxisome proliferator-activated receptor gamma (PPARγ) expression in BMSCs [297]. The senolytic compounds, dasatinib and quercetin, were found to prevent an age-dependent progression of disc degeneration in mice by preserving cell viability, phenotype, and matrix content via the regulation of the levels of cellular senescence markers p16INK4a and p19ARF; SASP molecules IL-6 and MMP13 [298]; and the natural plant polyphenols, curcumin and quercetin. This ameliorated skin cellular aging induced by UV irradiation and H2O2 stimulation through activating the TGF-β and Nrf2 signaling pathways, enhancing collagen production and antioxidant enzyme expression, and decreasing the expression of MMP-1, MMP-3, COX-2, TNF-α and IL-1 [299]. Cocoa polyphenols extract (CPE) was reported to attenuate senescent phenotypes in an H2O2-induced cellular senescence model by downregulating SA-β-Gal expression, promoting cell proliferation, and decreasing oxidative DNA damage and mitochondrial dysfunction by inhibiting mitochondrial reactive oxygen species (mtROS) generation through the mediation of SIRT1, SIRT3, FoxO3, and P53 [300]. β-Cryptoxanthin (BCX), a type of carotenoid, attenuated H2O2-induced oxidative stress and cellular senescence in HK-2 cells by promoting Nrf2 nuclear translocation [301]. Vitamin D3 attenuated doxorubicin-induced senescence and cell-cycle arrest in human aortic endothelial cells through the upregulation of IL-10 and FoxO3a expression via the fine modulation of p-AMPKα/SIRT1/FoxO3a complex activity [302]. Betulinic acid (BA), a kind of pentacyclic triterpenoid, is abundant in fruits such as Zizyphus sp., Dillenia sp., and Azanza sp. Treatment with BA promoted cellular proliferation and alleviated the cellular senescence of normal human dermal fibroblasts (NHDFs) via the inhibition of the type I interferon signaling pathway [303].
3.8. Other Anti-Aging Mechanisms
Food-derived bioactive compounds have also been found to exert anti-aging activity through other modes of action in addition to the mechanisms mentioned above. Telomeres are specialized structures found at the ends of linear chromosomes, containing a tandemly repeated sequence (TTAGGG) and associated protective proteins. Telomeres shorten with each cell division, and the main function of telomeres is to protect chromosome ends from fusion and degradation in proliferating cells [304,305,306]. Telomerase, a unique reverse transcriptase in cells, is able to add repetitive telomeric sequences de novo onto telomeric ends, thus leading to telomere restoration [307]. Numerous studies have proved that telomeres continually shorten with the aging process, which is also a risk factor for many age-related diseases [307]. Hence, telomerase activation in vivo has significant potential for delaying aging and alleviating aging-associated diseases [308,309,310,311]. For example, the terpenoid cycloastragenol (CA) and its biotransformation products showed anti-aging effects by improving telomerase activation [193,312,313]. Similarly, the polysaccharide extracted from Angelica sinensis polysaccharide (ASP) and Astragalus membranaceus polysaccharide (AMP) were shown to exert anti-aging activity by improving telomerase activity and regulating p53-p21 and p16-pRb pathways [44]. A recent study, which used cross-sectional data from the National Health and Nutrition Examination Surveys (NHANES) database from 1999 to 2002, also indicated that vitamin C was positively correlated with telomere length, with greater dietary vitamin C intake being associated with longer telomeres in a total of 7094 participants [314].
Mitochondria are essential not only for obtaining ATP from glucose and fatty acids but also in amino acid metabolism, pyridine synthesis, phospholipid modification and calcium regulation [19]. It is well known that mitochondrial dysfunction and decreased mitochondrial biogenesis are hallmarks of aging and play a role in speeding aging [315,316]. Polyphenols have been found to be able to delay aging through regulation of mitochondrial function and biogenesis. Resveratrol significantly extended the lifespan of mice fed a high-calorie diet by improving mitochondrial function [317]. Similarly, the polysaccharides from ginseng alleviated the aging of C. elegans by inducing the preferential synthesis of beneficial fatty acids [38], and the polysaccharides from the brown alga Sargassum fusiforme (SFPs) protected liver tissue in old male mice by improving energy metabolism [48]. Additionally, the polysaccharide from Chinese wolfberry Lycium barbarum reduced PM2.5-induced cell death and ameliorated cell morphology through the regulation of apoptosis and mitochondrial autophagy [35].
4. Conclusions and Perspectives
Human beings are entering an aging society globally. With the constant increase in the social pension burden, the discovery and development of safe and effective anti-aging approaches to prolong healthy lifespan are receiving increasing attention. Numerous studies have shown that both nutritional and pharmacological interventions can extend lifespan in a variety of model organisms, including yeast, nematodes, fruit flies, fish, mice and rats. In this review, we summarized the bioactive compounds from natural food sources that have the potential to prolong lifespan and prevent aging-associated diseases. These compounds include polysaccharides, polyphenols, carotenoids, sterols, terpenoids and vitamins, which are abundant in edible plants, algae, animals and fungi. The compounds have dual use in both food and medicine and show great potential for maintaining elderly health and prolonging healthy lifespan. However, there are still many issues that need to be studied and solved before they can be truly applied. The primary issues are as follows:
- Most of the compounds are mixtures and therefore need further purification in order to determine the exact molecule that exhibits the bioactive activity.
- A compound often has multiple modes of action. Therefore, for specific compounds, their modes of action require in-depth research.
- Lifespan extension is a direct and key indicator for evaluating the anti-aging efficiency of bioactive compounds. It is relatively easy to detect the lifespan of animals with short life cycles such as nematodes and fruit flies, but it is difficult to do so for human beings as they have much longer lifespans. Therefore, we need to search for and identify suitable and intuitive anti-aging indicators to examine the life-extension effects of the compounds on humans.
- Previous anti-aging experiments are often limited to research on the short-term effects of the compounds. Therefore, long-term and large-scale clinical trials are urgently needed to investigate the anti-aging effects of compounds.
Author Contributions
Conceptualization, S.Z.; writing—original draft preparation, L.S.; writing—review and editing, S.Z.; supervision, S.Z.; funding acquisition, S.Z. and L.S. All authors have read and agreed to the published version of the manuscript.
Funding
This work was supported by the Science and Technology Research Project of Hebei Higher Education Institutions (QN2023099) and Initiative Research Fund of Kashi University (022023184).
Data Availability Statement
Data will be made available on request.
Conflicts of Interest
The authors declare that they have no conflict of interest.
References
- World Population-Population Stat 2023. Available online: https://populationstat.com/ (accessed on 7 July 2023).
- World Population Prospects 2022. Available online: https://www.un.org/development/desa/pd/sites/www.un.org.development.desa.pd/files/wpp2022_summary_of_results.pdf (accessed on 5 June 2023).
- Schäfer, D. Aging, longevity, and diet: Historical remarks on calorie intake reduction. Gerontology 2005, 51, 126–130. [Google Scholar] [CrossRef] [PubMed]
- Zhang, Y.; Li, Q.; Niu, Y.; Wei, K.; Wang, X.; Niu, B.; Zhang, L. Research progress on aging mechanism and drugs and the role of stem cells in anti-aging process. Exp. Gerontol. 2023, 179, 112248. [Google Scholar] [CrossRef] [PubMed]
- Klass, M.R. A method for the isolation of longevity mutants in the nematode Caenorhabditis elegans and initial results. Mech. Ageing. Dev. 1983, 22, 279–286. [Google Scholar] [CrossRef] [PubMed]
- Lopez-Otin, C.; Blasco, M.A.; Partridge, L.; Serrano, M.; Kroemer, G. The hallmarks of aging. Cell 2013, 153, 1194–1217. [Google Scholar] [CrossRef]
- Schmeer, C.; Kretz, A.; Wengerodt, D.; Stojiljkovic, M.; Witte, O.W. Dissecting aging and senescence-current concepts and open lessons. Cells 2019, 8, 1446. [Google Scholar] [CrossRef] [PubMed]
- Van Voorhies, W.A. Metabolism and aging in the nematode Caenorhabditis elegans. Free Radic. Biol. Med. 2002, 33, 587–596. [Google Scholar]
- Harman, D. The free radical theory of aging: Effect of age on serum copper levels. J. Gerontol. 1965, 20, 151–153. [Google Scholar] [CrossRef]
- Harman, D. The aging process. Proc. Natl. Acad. Sci. USA 1981, 78, 7124–7128. [Google Scholar] [CrossRef]
- Hayflick, L.; Moorhead, P.S. The serial cultivation of human diploid cell strains. Exp. Cell Res. 1961, 25, 585–621. [Google Scholar] [CrossRef]
- Olovnikov, A.M. Telomeres, telomerase, and aging: Origin of the theory. Exp. Gerontol. 1996, 31, 443–448. [Google Scholar] [CrossRef]
- Gensler, H.L.; Bernstein, H. DNA damage as the primary cause of aging. Q. Rev. Biol. 1981, 56, 279–303. [Google Scholar] [CrossRef] [PubMed]
- Orgel, L.E. The maintenance of the accuracy of protein synthesis and its relevance to ageing. Proc. Natl. Acad. Sci. USA 1963, 49, 517–521. [Google Scholar] [CrossRef]
- Weismann, A. Essays upon Heredity and Kindred Biological Problems; Poulton, E.B., Selmar, S., Arthur, S.E., Eds.; Clarendon Press: Oxford, UK, 1889. [Google Scholar]
- Davalli, P.; Mitic, T.; Caporali, A.; Lauriola, A.; D’Arca, D. ROS, cell senescence, and novel molecular mechanisms in aging and age-related diseases. Oxid. Med. Cell. Longev. 2016, 2016, 3565127. [Google Scholar] [CrossRef] [PubMed]
- Fulop, T.; Larbi, A.; Pawelec, G.; Khalil, A.; Cohen, A.A.; Hirokawa, K.; Witkowski, J.M.; Franceschi, C. Immunology of aging: The birth of inflammaging. Clin. Rev. Allergy. Immunol. 2023, 64, 109–122. [Google Scholar] [CrossRef] [PubMed]
- Argüelles, S.; Guerrero-Castilla, A.; Cano, M.; Muñoz, M.F.; Ayala, A. Advantages and disadvantages of apoptosis in the aging process. Ann. N. Y. Acad. Sci. 2019, 1443, 20–33. [Google Scholar] [CrossRef]
- Lopez-Lluch, G.; Hernandez-Camacho, J.D.; Fernandez-Ayala, D.J.M.; Navas, P. Mitochondrial dysfunction in metabolism and ageing: Shared mechanisms and outcomes? Biogerontology 2018, 19, 461–480. [Google Scholar] [CrossRef]
- Mechchate, H.; El Allam, A.; El Omari, N.; El Hachlafi, N.; Shariati, M.A.; Wilairatana, P.; Mubarak, M.S.; Bouyahya, A. Vegetables and their bioactive compounds as anti-aging drugs. Molecules 2022, 27, 2316. [Google Scholar] [CrossRef]
- Hernandez, D.F.; Cervantes, E.L.; Luna-Vital, D.A.; Mojica, L. Food-derived bioactive compounds with anti-aging potential for nutricosmetic and cosmeceutical products. Crit. Rev. Food. Sci. Nutr. 2021, 61, 3740–3755. [Google Scholar] [CrossRef]
- Di Micco, R.; Krizhanovsky, V.; Baker, D.; d’Adda di Fagagna, F. Cellular senescence in ageing: From mechanisms to therapeutic opportunities. Nat. Rev. Mol. Cell Biol. 2021, 22, 75–95. [Google Scholar] [CrossRef]
- Herranz, N.; Gil, J. Mechanisms and functions of cellular senescence. J. Clin. Investig. 2018, 128, 1238–1246. [Google Scholar] [CrossRef]
- Lee, S.; Schmitt, C.A. The dynamic nature of senescence in cancer. Nat. Cell Biol. 2019, 21, 94–101. [Google Scholar] [CrossRef] [PubMed]
- Chuang, S.Y.; Lin, C.H.; Fang, J.Y. Natural compounds and aging: Between autophagy and inflammasome. Biomed. Res. Int. 2014, 2014, e297293. [Google Scholar] [CrossRef] [PubMed]
- Tundis, R.; Loizzo, M.R.; Bonesi, M.; Menichini, F. Potential role of natural compounds against skin aging. Curr. Med. Chem. 2015, 22, 1515–1538. [Google Scholar] [CrossRef]
- Taoerdahong, H.; Kadeer, G.; Chang, J.; Kang, J.; Ma, X.; Yang, F. A review concerning the polysaccharides found in edible and medicinal plants in Xinjiang. Molecules 2023, 28, 2054. [Google Scholar] [CrossRef]
- Vetvicka, V.; Vetvickova, J. Immune enhancing effects of WB365, a novel combination of Ashwagandha (Withania somnifera) and Maitake (Grifola frondosa) extracts. N. Am. J. Med. Sci. 2011, 3, 320–324. [Google Scholar] [CrossRef] [PubMed]
- Rossi, P.; Difrancia, R.; Quagliariello, V.; Savino, E.; Tralongo, P.; Randazzo, C.L.; Berretta, M. B-glucans from Grifola Frondosa and Ganoderma Lucidum in breast cancer: An example of complementary and integrative medicine. Oncotarget 2018, 9, 24837–24856. [Google Scholar] [CrossRef]
- Yu, Y.; Shen, M.; Song, Q.; Xie, J. Biological activities and pharmaceutical applications of polysaccharide from natural resources: A review. Carbohydr. Polym. 2018, 183, 91–101. [Google Scholar] [CrossRef]
- Tang, R.; Chen, X.; Dang, T.; Deng, Y.; Zou, Z.; Liu, Q.; Gong, G.; Song, S.; Ma, F.; Huang, L.; et al. Lycium barbarum polysaccharides extend the mean lifespan of Drosophila melanogaster. Food Funct. 2019, 10, 4231–4241. [Google Scholar] [CrossRef]
- Wang, Z.; Sun, Q.; Fang, J.; Wang, C.; Wang, D.; Li, M. The anti-aging activity of Lycium barbarum polysaccharide extracted by yeast fermentation: In vivo and in vitro studies. Int. J. Biol. Macromol. 2022, 209, 2032–2041. [Google Scholar] [CrossRef]
- Zheng, X.; Wang, J.; Bi, F.; Li, Y.; Xiao, J.; Chai, Z.; Li, Y.; Miao, Z.; Wang, Y. Protective effects of Lycium barbarum polysaccharide on ovariectomy-induced cognition reduction in aging mice. Int. J. Mol. Med. 2021, 48, 121. [Google Scholar] [CrossRef]
- Li, H.; Li, Z.; Peng, L.; Jiang, N.; Liu, Q.; Zhang, E.; Liang, B.; Li, R.; Zhu, H. Lycium barbarum polysaccharide protects human keratinocytes against UVB-induced photo-damage. Free. Radic. Res. 2017, 51, 200–210. [Google Scholar] [CrossRef] [PubMed]
- Zhu, S.; Li, X.; Dang, B.; Wu, F.; Wang, C.; Lin, C. Lycium barbarum polysaccharide protects HaCaT cells from PM2.5-induced apoptosis via inhibiting oxidative stress, ER stress and autophagy. Redox. Rep. 2022, 27, 32–44. [Google Scholar] [CrossRef]
- Xia, G.; Xin, N.; Liu, W.; Yao, H.; Hou, Y.; Qi, J. Inhibitory effect of Lycium barbarum polysaccharides on cell apoptosis and senescence is potentially mediated by the p53 signaling pathway. Mol. Med. Rep. 2014, 9, 1237–1241. [Google Scholar] [CrossRef] [PubMed]
- Fan, J.; Feng, H.; Yu, Y.; Sun, M.; Liu, Y.; Li, T.; Sun, X.; Liu, S.; Sun, M. Antioxidant activities of the polysaccharides of Chuanminshen violaceum. Carbohyd. Polym. 2017, 157, 629–636. [Google Scholar] [CrossRef] [PubMed]
- Sun, J.; Zhong, X.; Sun, D.; Xu, L.; Shi, L.; Sui, J.; Liu, Y. Anti-aging effects of polysaccharides from ginseng extract residues in Caenorhabditis elegans. Int. J. Biol. Macromol. 2023, 225, 1072–1084. [Google Scholar] [CrossRef] [PubMed]
- Liu, M.; Li, N.; Lu, X.; Shan, S.; Gao, X.; Cao, Y.; Lu, W. Sweet tea (Rubus Suavissmus S. Lee) polysaccharides promote the longevity of Caenorhabditis elegans through autophagy-dependent insulin and mitochondrial pathways. Int. J. Biol. Macromol. 2022, 207, 883–892. [Google Scholar] [CrossRef] [PubMed]
- Yang, S.; Sun, J.; Gu, D.; Li, P.; Yao, L.; Shi, D.; Guo, S.; Liu, C. Antioxidant activities of sulfated Codonopsis polysaccharides in acute oxidative stress. J. Food. Biochem. 2021, 45, e13974. [Google Scholar] [CrossRef]
- Doan, V.M.; Chen, C.; Lin, X.; Nguyen, V.P.; Nong, Z.; Li, W.; Chen, Q.; Ming, J.; Xie, Q.; Huang, R. Yulangsan polysaccharide improves redox homeostasis and immune impairment in D-galactose-induced mimetic aging. Food Funct. 2015, 6, 1712–1718. [Google Scholar] [CrossRef]
- Zhang, M.; Cui, S.; Mao, B.; Zhang, Q.; Zhao, J.; Tang, X.; Chen, W. Urolithin A produced by novel microbial fermentation possesses anti-aging effects by improving mitophagy and reducing reactive oxygen species in Caenorhabditis elegans. J. Agric. Food. Chem. 2023, 71, 6348–6357. [Google Scholar] [CrossRef]
- Kim, J.E.; Jang, S.G.; Lee, C.H.; Lee, J.Y.; Park, H.; Kim, J.H.; Lee, S.; Kim, H.S.; Park, E.-Y.; Lee, K.W.; et al. Beneficial effects on skin health using polysaccharides from red ginseng by-product. J. Food Biochem. 2019, 43, e12961. [Google Scholar] [CrossRef]
- Pu, X.; Yu, S.; Fan, W.; Liu, L.; Ma, X.; Ren, J. Guiqi polysaccharide protects the normal human fetal lung fibroblast WI-38 cells from H2O2-induced premature senescence. Int. J. Clin. Exp. Pathol. 2015, 8, 4398–4407. [Google Scholar]
- Li, N.; Li, Q.; He, X.; Gao, X.; Wu, L.; Xiao, M.; Cai, W.; Liu, B.; Zeng, F. Antioxidant and anti-aging activities of Laminaria japonica polysaccharide in Caenorhabditis elegans based on metabonomic analysis. Int. J. Biol. Macromol. 2022, 221, 346–354. [Google Scholar] [CrossRef] [PubMed]
- Zhang, Z.; Wang, X.; Pan, Y.; Wang, G.; Mao, G. The degraded polysaccharide from Pyropia haitanensis represses amyloid beta peptide-induced neurotoxicity and memory in vivo. Int. J. Biol. Macromol. 2019, 146, 725–729. [Google Scholar] [CrossRef]
- Wang, X.; Zhang, Z.; Zhou, H.; Sun, X.; Chen, X.; Xu, N. The anti-aging effects of Gracilaria lemaneiformis polysaccharide in Caenorhabditis elegans. Int. J. Biol. Macromol. 2019, 140, 600–604. [Google Scholar] [CrossRef] [PubMed]
- Chen, P.; Zhang, Y.; Xu, M.; Chen, H.; Zou, H.; Zhang, X.; Tong, H.; You, C.; Wu, M. Proteomic landscape of liver tissue in old male mice that are long-term treated with polysaccharides from Sargassum fusiforme. Food. Funct. 2020, 11, 3632–3644. [Google Scholar] [CrossRef] [PubMed]
- Chen, P.; He, D.; Zhang, Y.; Yang, S.; Chen, L.; Wang, S.; Zou, H.; Liao, Z.; Zhang, X.; Wu, M. Sargassum fusiforme polysaccharides activate antioxidant defense by promoting Nrf2-dependent cytoprotection and ameliorate stress insult during aging. Food Funct. 2016, 7, 4576–4588. [Google Scholar] [CrossRef]
- Chen, P.; Yang, S.; Hu, C.; Zhao, Z.; Liu, J.; Cheng, Y.; Wang, S.; Chen, Q.; Yu, P.; Zhang, X.; et al. Sargassum fusiforme polysaccharide rejuvenates the small intestine in mice through altering its physiology and gut microbiota composition. Curr. Mol. Med. 2017, 17, 350–358. [Google Scholar] [PubMed]
- Zhang, X.; Liu, L.; Luo, J.; Peng, X. Anti-aging potency correlates with metabolites from in vitro fermentation of edible fungal polysaccharides using human fecal intestinal microflora. Food. Funct. 2022, 13, 11592–11603. [Google Scholar] [CrossRef]
- Tripodi, F.; Falletta, E.; Leri, M.; Angeloni, C.; Beghelli, D.; Giusti, L.; Milanesi, R.; Sampaio-Marques, B.; Ludovico, P.; Goppa, L.; et al. Anti-aging and neuroprotective properties of Grifola frondosa and Hericium erinaceus extracts. Nutrients 2022, 14, 4368. [Google Scholar] [CrossRef]
- Zhang, C.; Gao, Z.; Hu, C.; Zhang, J.; Sun, X.; Rong, C.; Jia, L. Antioxidant, antibacterial and anti-aging activities of intracellular zinc polysaccharides from Grifola frondosa SH-05. Int. J. Biol. Macromol. 2017, 95, 778–787. [Google Scholar] [CrossRef]
- Song, F.; Gao, Z.; Liu, W.; Li, H.; Zhang, Y.; Feng, Y.; Song, X.; Wang, W.; Zhang, J.; Huang, C.; et al. Characterization, antioxidant, anti-aging and organ protective effects of sulfated polysaccharides from Flammulina velutipes. Molecules 2019, 24, 3517. [Google Scholar]
- Duan, H.; Li, J.; Fan, L. Agaricus bisporus polysaccharides ameliorates behavioural deficits in D-galactose-induced aging mice: Mediated by gut microbiota. Foods 2023, 12, 424. [Google Scholar] [CrossRef] [PubMed]
- Li, S.; Liu, M.; Zhang, C.; Tian, C.; Wang, X.; Song, X.; Jing, H.; Gao, Z.; Ren, Z.; Liu, W.; et al. Purification, in vitro antioxidant and in vivo anti-aging activities of soluble polysaccharides by enzyme-assisted extraction from Agaricus bisporus. Int. J. Biol. Macromol. 2018, 109, 457–466. [Google Scholar] [CrossRef]
- Li, S.; Liu, H.; Wang, W.; Wang, X.; Zhang, C.; Zhang, J.; Jing, H.; Ren, Z.; Gao, Z.; Song, X.; et al. Antioxidant and anti-aging effects of acidic-extractable polysaccharides by Agaricus bisporus. Int. J. Biol. Macromol. 2018, 106, 1297–1306. [Google Scholar] [CrossRef]
- Song, L.; Zhou, Y.; Ni, S.; Wang, X.; Yuan, J.; Zhang, Y.; Zhang, S. Dietary intake of β-glucans can prolong lifespan and exert an antioxidant action on aged fish Nothobranchius guentheri. Rejuvenation. Res. 2020, 23, 293–301. [Google Scholar] [CrossRef] [PubMed]
- Song, L.; Yuan, J.; Ni, S.; Zhou, Y.; Wang, X.; Chen, Y.; Zhang, S. Enhancement of adaptive immune responses of aged mice by dietary intake of β-glucans, with special emphasis on anti-aging activity. Mol. Immunol. 2020, 117, 160–167. [Google Scholar] [CrossRef]
- Shen, T.; Duan, C.; Chen, B.; Li, M.; Ruan, Y.; Xu, D.; Shi, D.; Yu, D.; Li, J.; Wang, C. Tremella fuciformis polysaccharide suppresses hydrogen peroxide-triggered injury of human skin fibroblasts via upregulation of SIRT1. Mol. Med. Rep. 2017, 16, 1340–1346. [Google Scholar] [CrossRef]
- Yue, Y.; Li, Z.; Li, P.; Song, N.; Li, B.; Lin, W.; Liu, S. Antiviral activity of a polysaccharide from Laminaria japonica against enterovirus 71. Biomed. Pharmacother. 2017, 96, 256–262. [Google Scholar] [CrossRef]
- Ding, Q.; Yang, D.; Zhang, W.; Lu, Y.; Zhang, M.; Wang, L.; Li, X.; Zhou, L.; Wu, Q.; Pan, W.; et al. Antioxidant and anti-aging activities of the polysaccharide TLH-3 from Tricholoma lobayense. Int. J. Biol. Macromol. 2016, 85, 133–140. [Google Scholar] [CrossRef]
- Wu, Y.J.; Wei, Z.X.; Zhang, F.M.; Linhardt, R.J.; Sun, P.L.; Zhang, A.Q. Structure, bioactivities and applications of the polysaccharides from Tremella fuciformis mushroom: A review. Int. J. Biol. Macromol. 2019, 121, 1005–1010. [Google Scholar] [CrossRef]
- Singla, R.K.; Dubey, A.K.; Garg, A.; Sharma, R.K.; Fiorino, M.; Ameen, S.M.; Haddad, M.A.; Al-Hiary, M. Natural polyphenols: Chemical classification, definition of classes, subcategories, and structures. J. AOAC Int. 2019, 102, 1397–1400. [Google Scholar] [CrossRef] [PubMed]
- Sahiner, M.; Sahiner, N.; Sagbas, S.; Fullerton, M.L.; Blake, D.A. Fabrication of biodegradable poly (naringin) particles with antioxidant activity and low toxicity. ACS. Omega 2018, 3, 17359–17367. [Google Scholar] [CrossRef]
- Xu, D.P.; Li, Y.; Meng, X.; Zhou, T.; Zhou, Y.; Zheng, J.; Zhang, J.J.; Li, H.B. Natural antioxidants in foods and medicinal plants: Extraction, assessment and resources. Int. J. Mol. Sci. 2017, 18, 96. [Google Scholar] [CrossRef]
- Uddin, N.; Muhammad, N.; Nisar, M.; Aisha; Ali, N.; Ullah, R.; Ali, E.A.; Khan, A.A.; Rahman, I.U.; Khan, A.; et al. Distribution of polyphenolic compounds, antioxidant potential, and free amino acids in Ziziphus fruits extract; a study for determining the influence of wider geography. Food. Sci. Nutr. 2022, 10, 1414–1430. [Google Scholar] [CrossRef] [PubMed]
- Besednova, N.N.; Andryukov, B.G.; Zaporozhets, T.S.; Kryzhanovsky, S.P.; Kuznetsova, T.A.; Fedyanina, L.N.; Makarenkova, I.D.; Zvyagintseva, T.N. Algae polyphenolic compounds and modern antibacterial strategies: Current achievements and immediate prospects. Biomedicines 2020, 8, 342. [Google Scholar] [CrossRef]
- Sun, C.; Zhao, C.; Guven, E.C.; Paoli, P.; Simal-Gandara, J.; Ramkumar, K.M.; Wang, S.; Buleu, F.; Pah, A.; Turi, V.; et al. Dietary polyphenols as antidiabetic agents: Advances and opportunities. Food. Front. 2020, 1, 18–44. [Google Scholar] [CrossRef]
- Niedzwiecki, A.; Roomi, M.; Kalinovsky, T.; Rath, M. Anticancer efficacy of polyphenols and their combinations. Nutrients 2016, 8, 552. [Google Scholar] [CrossRef]
- Meng, T.; Xiao, D.; Muhammed, A.; Deng, J.; Chen, L.; He, J. Anti-inflammatory action and mechanisms of resveratrol. Molecules 2021, 26, 229. [Google Scholar] [CrossRef]
- Zhou, D.D.; Luo, M.; Huang, S.Y.; Saimaiti, A.; Shang, A.; Gan, R.Y.; Li, H.B. Effects and mechanisms of resveratrol on aging and age-related diseases. Oxid. Med. Cell. Longev. 2021, 2021, 9932218. [Google Scholar] [CrossRef]
- Mateș, L.; Rusu, M.E.; Popa, D.S. Phytochemicals and biological activities of walnut septum: A systematic review. Antioxidants 2023, 12, 604. [Google Scholar] [CrossRef]
- Zheng, S.Q.; Huang, X.B.; Xing, T.K.; Ding, A.J.; Wu, G.S.; Luo, H.R. Chlorogenic acid extends the lifespan of Caenorhabditis elegans via insulin/IGF-1 signaling pathway. J. Gerontol. A. Biol. Sci. Med. Sci. 2017, 72, 464–472. [Google Scholar]
- Yue, Y.; Shen, P.; Xu, Y.; Park, Y. p-Coumaric acid improves oxidative and osmosis stress responses in Caenorhabditis elegans. J. Sci. Food. Agr. 2019, 99, 1190–1197. [Google Scholar] [CrossRef] [PubMed]
- Gutierrez-Zetina, S.M.; González-Manzano, S.; Ayuda-Durán, B.; Santos-Buelga, C.; González-Paramás, A.M. Caffeic and dihydrocaffeic acids promote longevity and increase stress resistance in Caenorhabditis elegans by modulating expression of stress-related genes. Molecules 2021, 26, 1517. [Google Scholar] [CrossRef] [PubMed]
- Sugawara, T.; Sakamoto, K. Quercetin enhances motility in aged and heat-stressed Caenorhabditis elegans nematodes by modulating both HSF-1 activity, and insulin-like and p38-MAPK signaling. PLoS. ONE 2020, 15, e0238528. [Google Scholar] [CrossRef]
- Kim, S.G.; Sung, J.Y.; Kim, J.R.; Choi, H.C. Quercetin-induced apoptosis ameliorates vascular smooth muscle cell senescence through AMP-activated protein kinase signaling pathway. Korean. J. Physiol. Pharmacol. 2020, 24, 69–79. [Google Scholar] [CrossRef] [PubMed]
- Bermejo-Bescós, P.; Jiménez-Aliaga, K.L.; Benedí, J.; Martín-Aragón, S. A diet containing rutin ameliorates brain intracellular redox homeostasis in a mouse model of Alzheimer’s disease. Int. J. Mol. Sci. 2023, 24, 4863. [Google Scholar] [CrossRef]
- Chen, W.; Muller, D.; Richling, E.; Wink, M. Anthocyanin-rich purple wheat prolongs the life span of Caenorhabditis elegans probably by activating the DAF-16/FOXO transcription factor. J. Agric. Food. Chem. 2013, 61, 3047–3053. [Google Scholar] [CrossRef]
- Golubev, D.; Zemskaya, N.; Shevchenko, O.; Shaposhnikov, M.; Kukuman, D.; Patov, S.; Punegov, V.; Moskalev, A. Honeysuckle extract (Lonicera pallasii L.) exerts antioxidant properties and extends the lifespan and healthspan of Drosophila melanogaster. Biogerontology 2022, 23, 215–235. [Google Scholar] [CrossRef]
- Jayarathne, S.; Ramalingam, L.; Edwards, H.; Vanapalli, S.A.; Moustaid-Moussa, N. Tart cherry increases lifespan in Caenorhabditis elegans by altering metabolic signaling pathways. Nutrients 2020, 12, 1482. [Google Scholar] [CrossRef]
- Chandrashekara, K.T.; Shakarad, M.N. Aloe vera or resveratrol supplementation in larval diet delays adult aging in the fruit fly, Drosophila melanogaster. J. Gerontol. A-Biol. 2011, 66, 965–971. [Google Scholar] [CrossRef]
- Yu, X.; Li, G.R. Effects of resveratrol on longevity, cognitive ability and aging-related histological markers in the annual fish Nothobranchius guentheri. Exp. Gerontol. 2012, 47, 940–949. [Google Scholar] [CrossRef] [PubMed]
- Zhu, H.; Li, X.; Qiao, M.; Sun, X.; Li, G. Resveratrol alleviates inflammation and ER stress through SIRT1/NRF2 to delay ovarian aging in a short-lived fish. J. Gerontol. A. Biol. Sci. Med. Sci. 2023, 78, 596–602. [Google Scholar] [CrossRef]
- Gerhardt, E.; Graber, S.; Szego, E.M.; Moisoi, N.; Martins, L.M.; Outeiro, T.F.; Kermer, P. Idebenone and resveratrol extend lifespan and improve motor function of HtrA2 knockout mice. PLoS. ONE 2011, 6, 7. [Google Scholar] [CrossRef] [PubMed]
- Xiong, W.X.; Chai, Z.T.; Wang, B.; Zhou, G.X.; Cang, J.; Xue, Z.G.; Ge, S.J. Resveratrol alleviates learning and memory impairment in aged rats after general anesthesia with sevoflurane and nitrous oxide via SIRT1-p53 signaling pathway. Int. J. Clin. Exp. Med. 2016, 9, 21118–21130. [Google Scholar]
- Liu, S.; Zheng, Z.; Ji, S.; Liu, T.; Hou, Y.; Li, S.; Li, G. Resveratrol reduces senescence-associated secretory phenotype by SIRT1/NF-κB pathway in gut of the annual fish Nothobranchius guentheri. Fish Shellfish Immunol. 2018, 80, 473–479. [Google Scholar] [CrossRef]
- Yuan, J.; Lu, L.; Zhang, Z.; Zhang, S. Dietary intake of resveratrol enhances the adaptive immunity of aged rats. Rejuvenation Res. 2012, 15, 507–515. [Google Scholar] [CrossRef] [PubMed]
- Ginés, C.; Cuesta, S.; Kireev, R.; García, C.; Rancan, L.; Paredes, S.D.; Vara, E.; Tresguerres, J.A.F. Protective effect of resveratrol against inflammation, oxidative stress and apoptosis in pancreas of aged SAMP8 mice. Exp. Gerontol. 2017, 90, 61–70. [Google Scholar] [CrossRef]
- Keowkase, R.; Shoomarom, N.; Bunargin, W.; Sitthithaworn, W.; Weerapreeyakul, N. Sesamin and sesamolin reduce amyloid-beta toxicity in a transgenic Caenorhabditis elegans. Biomed. Pharmacother. 2018, 107, 656–664. [Google Scholar] [CrossRef]
- Yaguchi, Y.; Komura, T.; Kashima, N.; Tamura, M.; Kage-Nakadai, E.; Saeki, S.; Terao, K.; Nishikawa, Y. Influence of oral supplementation with sesamin on longevity of Caenorhabditis elegans and the host defense. Eur. J. Nutr. 2014, 53, 1659–1668. [Google Scholar] [CrossRef]
- Saul, N.; Pietsch, K.; Menzel, R.; Sturzenbaum, S.R.; Steinberg, C.E. The longevity effect of tannic acid in Caenorhabditis elegans: Disposable soma meets hormesis. J. Gerontol. A. Biol. Sci. Med. Sci. 2010, 65, 626–635. [Google Scholar] [CrossRef]
- Saul, N.; Pietsch, K.; Sturzenbaum, S.R.; Menzel, R.; Steinberg, C.E. Diversity of polyphenol action in Caenorhabditis elegans: Between toxicity and longevity. J. Nat. Prod. 2011, 74, 1713–1720. [Google Scholar] [CrossRef]
- Chen, Y.; Onken, B.; Chen, H.; Zhang, X.; Driscoll, M.; Cao, Y.; Huang, Q. Healthy lifespan extension mediated by oenothein B isolated from Eucalyptus grandis ⅹ Eucalyptus urophylla GL9 in Caenorhabditis elegans. Food. Funct. 2020, 11, 2439–2450. [Google Scholar] [CrossRef]
- Chen, Y.; Onken, B.; Chen, H.; Xiao, S.; Liu, X.; Driscoll, M.; Cao, Y.; Huang, Q. Mechanism of longevity extension of Caenorhabditis elegans induced by pentagalloyl glucose isolated from eucalyptus leaves. J. Agric. Food. Chem. 2014, 62, 3422–3431. [Google Scholar] [CrossRef] [PubMed]
- Majidinia, M.; Karimian, A.; Alemi, F.; Yousefi, B.; Safa, A. Targeting miRNAs by polyphenols: Novel therapeutic strategy for aging. Biochem. Pharmacol. 2020, 173, 113688. [Google Scholar] [CrossRef] [PubMed]
- Chen, P.; Chen, F.; Guo, Z.; Lei, J.; Zhou, B. Recent advancement in bioeffect, metabolism, stability, and delivery systems of apigenin, a natural flavonoid compound: Challenges and perspectives. Front. Nutr. 2023, 10, 1221227. [Google Scholar] [CrossRef] [PubMed]
- Manzoor, M.F.; Ahmad, N.; Ahmed, Z.; Siddique, R.; Zeng, X.A.; Rahaman, A.; Muhammad Aadil, R.; Wahab, A. Novel extraction techniques and pharmaceutical activities of luteolin and its derivatives. J. Food. Biochem. 2019, 43, e12974. [Google Scholar] [CrossRef]
- El Menyiy, N.; Aboulaghras, S.; Bakrim, S.; Moubachir, R.; Taha, D.; Khalid, A.; Abdalla, A.N.; Algarni, A.S.; Hermansyah, A.; Ming, L.C.; et al. Genkwanin: An emerging natural compound with multifaceted pharmacological effects. Biomed. Pharmacother. 2023, 165, 115159. [Google Scholar] [CrossRef] [PubMed]
- Lee, J.H.; Zhou, H.Y.; Cho, S.Y.; Kim, Y.S.; Lee, Y.S.; Jeong, C.S. Anti-inflammatory mechanisms of apigenin: Inhibition of cyclooxygenase-2 expression, adhesion of monocytes to human umbilical vein endothelial cells, and expression of cellular adhesion molecules. Arch. Pharm. Res. 2007, 30, 1318–1327. [Google Scholar] [CrossRef]
- Patel, M.; Singh, S. Apigenin attenuates functional and structural alterations via targeting NF-kB/Nrf2 signaling pathway in LPS-induced Parkinsonism in experimental rats: Apigenin attenuates LPS-induced Parkinsonism in experimental rats. Neurotox. Res. 2022, 40, 941–960. [Google Scholar] [CrossRef]
- Yan, F.J.; Chen, Y.S.; Azat, R.; Zheng, X.D. Mulberry anthocyanin extract ameliorates oxidative damage in HepG2 cells and prolongs the lifespan of Caenorhabditis elegans through MAPK and Nrf2 pathways. Oxid. Med. Cell. Longev. 2017, 2017, 7956158. [Google Scholar] [CrossRef]
- Malaguarnera, L. Influence of resveratrol on the immune response. Nutrients 2019, 11, 946. [Google Scholar] [CrossRef]
- Salehi, B.; Mishra, A.P.; Nigam, M.; Sener, B.; Kilic, M.; Sharifi-Rad, M.; Valere Tsouh Fokou, P.; Cruz-Martins, N.; Sharifi-Rad, J. Resveratrol: A double-edged sword in health benefits. Biomedicines 2018, 6, 91. [Google Scholar] [CrossRef]
- Zhang, J. Resveratrol inhibits insulin responses in a SirT1-independent pathway. Biochem. J. 2006, 397, 519–527. [Google Scholar] [CrossRef]
- Desjardins, D.; Cacho-Valadez, B.; Liu, J.L.; Wang, Y.; Yee, C.; Bernard, K.; Khaki, A.; Breton, L.; Hekimi, S. Antioxidants reveal an inverted U-shaped dose-response relationship between reactive oxygen species levels and the rate of aging in Caenorhabditis elegans. Aging Cell 2017, 16, 104–112. [Google Scholar] [CrossRef] [PubMed]
- Guerrero-Legarreta, I.; López-Hernández, E.; Armenta-López, R.E.; García Barrientos, R. Pigmentos. In Química de Alimentos; Badui-Dergal, S., Ed.; Pearson: Mexico City, Mexico, 2013; p. 379. [Google Scholar]
- Schawartz, S.J.; Cooperstone, J.L.; Cichon, M.J.; von Elbe, J.H.; Giusti, M.M. Colorants. In Fennema’s Food Chemistry; Damodaran, S., Parkin, K.L., Eds.; CRC Press Taylor and Francis: Boca Raton, FL, USA, 2017; p. 681. [Google Scholar]
- Saini, R.K.; Nile, S.H.; Park, S.W. Carotenoids from fruits and vegetables: Chemistry, analysis, occurrence, bioavailability and biological activities. Food. Res. Int. 2015, 76, 735–750. [Google Scholar] [CrossRef] [PubMed]
- Torres-Rodríguez, A.; Salinas-Moreno, Y.; Valle-Guadarrama, S.; Alia-Tejacal, I. Soluble phenols and antioxidant activity in mamey sapote (Pouteria sapota) fruits in postharvest. Food. Res. Int. 2011, 44, 1956–1961. [Google Scholar] [CrossRef]
- Zheng, W.V.; Xu, W.; Li, Y.; Qin, J.; Zhou, T.; Li, D.; Xu, Y.; Cheng, X.; Xiong, Y.; Chen, Z. Anti-aging effect of β-carotene through regulating the KAT7-P15 signaling axis, inflammation and oxidative stress process. Cell. Mol. Biol. Lett. 2022, 27, 86. [Google Scholar] [CrossRef]
- Hu, W.; Dai, D.; Li, W. Anti-aging effect of Blakeslea trispora powder on adult mice. Biotechnol. Lett. 2013, 35, 1309–1315. [Google Scholar] [CrossRef]
- Liu, X.; Lin, X.; Zhang, S.; Guo, C.; Li, J.; Mi, Y.; Zhang, C. Lycopene ameliorates oxidative stress in the aging chicken ovary via activation of Nrf2/HO-1 pathway. Aging 2018, 10, 2016–2036. [Google Scholar] [CrossRef]
- Colmán-Martínez, M.; Martínez-Huélamo, M.; Valderas-Martínez, P.; Arranz-Martínez, S.; Almanza-Aguilera, E.; Corella, D.; Estruch, R.; Lamuela-Raventós, R.M. trans-Lycopene from tomato juice attenuates inflammatory biomarkers in human plasma samples: An intervention trial. Mol. Nutr. Food. Res. 2017, 61, 1600993. [Google Scholar] [CrossRef]
- Liu, C.B.; Wang, R.; Yi, Y.F.; Gao, Z.; Chen, Y.Z. Lycopene mitigates β-amyloid induced inflammatory response and inhibits NF-κB signaling at the choroid plexus in early stages of Alzheimer’s disease rats. J. Nutr. Biochem. 2018, 53, 66–71. [Google Scholar] [CrossRef]
- Krishnaswamy, V.K.D.; Alugoju, P.; Periyasamy, L. Effect of short-term oral supplementation of crocin on age-related oxidative stress, cholinergic, and mitochondrial dysfunction in rat cerebral cortex. Life Sci. 2020, 263, 118545. [Google Scholar] [CrossRef] [PubMed]
- Chen, Z.; Xiao, J.; Liu, H.; Yao, K.; Hou, H.; Cao, Y.; Liu, X. Astaxanthin attenuates oxidative stress and immune impairment in d-galactose-induced aging in rats by activating the Nrf2/Keap1 pathway and suppressing the NF-κB pathway. Food. Funct. 2020, 11, 8099–8111. [Google Scholar] [CrossRef] [PubMed]
- Al-Amin, M.M.; Akhter, S.; Hasan, A.T.; Alam, T.; Nageeb Hasan, S.M.; Saifullah, A.R.; Shohel, M. The antioxidant effect of astaxanthin is higher in young mice than aged: A region specific study on brain. Metab. Brain. Dis. 2015, 30, 1237–1246. [Google Scholar] [CrossRef]
- Sj, S.; Veerabhadrappa, B.; Subramaniyan, S.; Dyavaiah, M. Astaxanthin enhances the longevity of Saccharomyces cerevisiae by decreasing oxidative stress and apoptosis. FEMS Yeast Res. 2019, 19, foy113. [Google Scholar] [CrossRef]
- Wen, X.; Huang, A.; Hu, J.; Zhong, Z.; Liu, Y.; Li, Z.; Pan, X.; Liu, Z. Neuroprotective effect of astaxanthin against glutamate-induced cytotoxicity in HT22 cells: Involvement of the Akt/GSK-3β pathway. Neuroscience 2015, 303, 558–568. [Google Scholar] [CrossRef]
- Song, L.; Leng, K.; Xiao, K.; Zhang, S. Administration of krill oil extends lifespan of fish Nothobranchius guentheri via enhancement of antioxidant system and suppression of NF-κB pathway. Fish. Physiol. Biochem. 2022, 48, 1057–1073. [Google Scholar] [CrossRef]
- Li, J.; Xian, L.; Zheng, R.; Wang, Y.; Wan, X.; Liu, Y. Canthaxanthin shows anti-liver aging and anti-liver fibrosis effects by down-regulating inflammation and oxidative stress in vivo and in vitro. Int. Immunopharmacol. 2022, 110, 108942. [Google Scholar] [CrossRef]
- Philips, N.; Keller, T.; Hendrix, C.; Hamilton, S.; Arena, R.; Tuason, M.; Gonzalez, S. Regulation of the extracellular matrix remodeling by lutein in dermal fibroblasts, melanoma cells, and ultraviolet radiation exposed fibroblasts. Arch. Dermatol. Res. 2007, 299, 373–379. [Google Scholar] [CrossRef] [PubMed]
- Chae, S.; Park, S.; Park, G. Lutein protects human retinal pigment epithelial cells from oxidative stress-induced cellular senescence. Mol. Med. Rep. 2018, 18, 5182–5190. [Google Scholar] [CrossRef]
- Hadad, N.; Levy, R. The synergistic anti-inflammatory effects of lycopene, lutein, β-carotene, and carnosic acid combinations via redox-based inhibition of NF-κB signaling. Free Rad. Biol. Med. 2012, 53, 1381–1391. [Google Scholar] [CrossRef]
- Morris, M.C.; Wang, Y.; Barnes, L.L.; Bennett, D.A.; Dawson-Hughes, B.; Booth, S.L. Nutrients and bioactives in green leafy vegetables and cognitive decline: Prospective study. Neurology 2018, 90, e214–e222. [Google Scholar] [CrossRef] [PubMed]
- Baba, S.A.; Malik, A.H.; Wani, Z.A.; Mohiuddin, T.; Shah, Z.; Abbas, N.; Ashraf, N. Phytochemical analysis and antioxidant activity of different tissue types of Crocus sativus and oxidative stress alleviating potential of saffron extract in plants, bacteria, and yeast. S. Afr. J. Bot. 2015, 99, 80–87. [Google Scholar] [CrossRef]
- Seabra, L.M.A.J.; Pedrosa, L.F.C. Astaxanthin: Structural and functional aspects. Rev. Nutrio. 2010, 23, 1041–1050. [Google Scholar] [CrossRef]
- Liu, X.; Liu, H.; Chen, Z.; Xiao, J.; Cao, Y. DAF-16 acts as the “hub” of astaxanthin’s anti-aging mechanism to improve aging-related physiological functions in Caenorhabditis elegans. Food. Funct. 2021, 12, 9098–9110. [Google Scholar] [CrossRef]
- Ding, F.; Zhao, Y. Astaxanthin induces transcriptomic responses associated with lifespan extension in Caenorhabditis elegans. Antioxidants 2022, 11, 2115. [Google Scholar] [CrossRef]
- Sudharshan, S.J.; Dyavaiah, M. Astaxanthin protects oxidative stress mediated DNA damage and enhances longevity in Saccharomyces cerevisiae. Biogerontology 2021, 22, 81–100. [Google Scholar] [CrossRef]
- Hartmann, M.A. Plant sterols and the membrane environment. Trends. Plant. Sci. 1998, 3, 170–175. [Google Scholar] [CrossRef]
- Piironen, V.; Lindsay, D.G.; Miettinen, T.A.; Toivo, J.; Lampi, A.M. Plant sterols: Biosynthesis, biological function and their importance to human nutrition. J. Sci. Food. Agric. 2000, 80, 939–966. [Google Scholar] [CrossRef]
- Chen, S.; Yong, T.; Zhang, Y.; Su, J.; Jiao, C.; Xie, Y. Anti-tumor and anti-angiogenic ergosterols from Ganoderma lucidum. Front. Chem. 2017, 5, 85. [Google Scholar] [CrossRef]
- Hu, Z.; He, B.; Ma, L.; Sun, Y.; Niu, Y.; Zeng, B. Recent advances in ergosterol biosynthesis and regulation mechanisms in Saccharomyces cerevisiae. Indian. J. Microbiol. 2017, 57, 270–277. [Google Scholar] [CrossRef] [PubMed]
- Ibrahim, S.R.M.; Mohamed, G.A.; Al Haidari, R.A.; Soliman, A.A.; Asfour, H.Z.; Zayed, M.F. Fusaristerol A: A new cytotoxic and antifungal ergosterol fatty acid ester from the endophytic fungus Fusarium sp. associated with Mentha longifolia roots. Phcog. Mag. 2018, 14, 308–311. [Google Scholar] [CrossRef]
- Song, L.; Li, C.; Wu, F.; Zhang, S. Dietary intake of diosgenin delays aging of male fish Nothobranchius guentheri through modulation of multiple pathways that play prominent roles in ROS production. Biogerontology 2022, 23, 201–213. [Google Scholar] [CrossRef] [PubMed]
- Haiyuan, Y.U.; Shen, X.; Liu, D.; Hong, M.; Lu, Y. The protective effects of β-sitosterol and vermicularin from Thamnolia vermicularis (Sw.) Ach. against skin aging in vitro. An. Acad. Bras. Cienc. 2019, 91, e20181088. [Google Scholar] [CrossRef]
- Ji, Z.H.; Xu, Z.Q.; Zhao, H.; Yu, X.Y. Neuroprotective effect and mechanism of daucosterol palmitate in ameliorating learning and memory impairment in a rat model of Alzheimer’s disease. Steroids 2017, 119, 31–35. [Google Scholar] [CrossRef]
- Hah, Y.S.; Lee, W.K.; Lee, S.; Kim, E.J.; Lee, J.H.; Lee, S.J.; Ji, Y.H.; Kim, S.G.; Lee, H.H.; Hong, S.Y.; et al. β-Sitosterol attenuates dexamethasone-induced muscle atrophy via regulating FoxO1-dependent signaling in C2C12 cell and mice model. Nutrients 2022, 14, 2894. [Google Scholar] [CrossRef]
- Shi, C.; Luo, X.; Wang, J.; Long, D. Incorporation of β-sitosterol into the membrane prevents tumor necrosis factor-α-induced nuclear factor-κB activation and gonadotropin-releasing hormone decline. Steroids 2015, 96, 1–6. [Google Scholar] [CrossRef]
- Jeremy, M.; Gurusubramanian, G.; Roy, V.K. Vitamin D3 regulates apoptosis and proliferation in the testis of D-galactose-induced aged rat model. Sci. Rep. 2019, 9, 14103. [Google Scholar] [CrossRef]
- Halicka, H.D.; Zhao, H.; Li, J.; Traganos, F.; Studzinski, G.P.; Darzynkiewicz, Z. Attenuation of constitutive DNA damage signaling by 1,25-dihydroxyvitamin D3. Aging 2012, 4, 270–278. [Google Scholar] [CrossRef]
- Sun, Y.; Lin, Y.; Cao, X.; Xiang, L.; Qi, J. Sterols from Mytilidae show anti-aging and neuroprotective effects via anti-oxidative activity. Int. J. Mol. Sci. 2014, 15, 21660–21673. [Google Scholar] [CrossRef]
- Weng, Y.; Xiang, L.; Matsuura, A.; Zhang, Y.; Huang, Q.; Qi, J. Ganodermasides A and B, two novel anti-aging ergosterols from spores of a medicinal mushroom Ganoderma lucidum on yeast via UTH1 gene. Bioorg. Med. Chem. 2010, 18, 999–1002. [Google Scholar] [CrossRef]
- Long, H.; Qiu, X.; Cao, L.; Han, R. Discovery of the signal pathways and major bioactive compounds responsible for the anti-hypoxia effect of Chinese cordyceps. J. Ethnopharmacol. 2021, 277, 114215. [Google Scholar] [CrossRef] [PubMed]
- Racette, S.B.; Lin, X.; Ma, L.; Ostlund, R.E., Jr. Natural dietary phytosterols. J. AOAC Int. 2015, 98, 679–684. [Google Scholar] [CrossRef]
- Nes, W.D. Biosynthesis of cholesterol and other sterols. Chem. Rev. 2011, 111, 6423–6451. [Google Scholar] [CrossRef]
- Moreau, R.A.; Whitaker, B.D.; Hicks, K.B. Phytosterols, phytostanols, and their conjugates in foods: Structural diversity, quantitative analysis, and health-promoting uses. Prog. Lipid. Res. 2002, 41, 457–500. [Google Scholar] [CrossRef] [PubMed]
- Cohn, J.S.; Kamili, A.; Wat, E.; Chung, R.W.; Tandy, S. Reduction in intestinal cholesterol absorption by various food components: Mechanisms and implications. Atheroscler. Suppl. 2010, 11, 45–48. [Google Scholar] [CrossRef]
- Gupta, A.K.; Savopoulos, C.G.; Ahuja, J.; Hatzitolios, A.I. Role of phytosterols in lipid-lowering: Current perspectives. QJM 2011, 104, 301–308. [Google Scholar] [CrossRef] [PubMed]
- Ogbe, R.J.; Ochalefu, D.O.; Mafulul, S.G. A review on dietary phytosterols: Their occurrence, metabolism and health benefits. Asian. J. Plant. Sci. Res. 2015, 5, 10–21. [Google Scholar]
- Tieu, E.W.; Li, W.; Chen, J.; Baldisseri, D.M.; Slominski, A.T.; Tuckey, R.C. Metabolism of cholesterol, vitamin D3 and 20-hydroxyvitamin D3 incorporated into phospholipid vesicles by human CYP27A1. J. Steroid. Biochem. Mol. Biol. 2012, 129, 163–171. [Google Scholar] [CrossRef]
- Benedik, E. Sources of vitamin D for humans. Int. J. Vitam. Nutr. Res. 2022, 92, 118–125. [Google Scholar] [CrossRef]
- Blomberg Jensen, M.; Nielsen, J.E.; Jørgensen, A.; Rajpert-De Meyts, E.; Kristensen, D.M.; Jørgensen, N.; Skakkebaek, N.E.; Juul, A.; Leffers, H. Vitamin D receptor and vitamin D metabolizing enzymes are expressed in the human male reproductive tract. Hum. Reprod. 2010, 25, 1303–1311. [Google Scholar] [CrossRef] [PubMed]
- Shahrokhi, S.Z.; Ghaffari, F.; Kazerouni, F. Role of vitamin D in female reproduction. Clin. Chim. Acta. 2016, 455, 33–38. [Google Scholar] [CrossRef]
- Kwiecinski, G.G.; Petrie, G.I.; DeLuca, H.F. Vitamin D is necessary for reproductive functions of the male rat. J. Nutr. 1989, 119, 741–744. [Google Scholar] [CrossRef]
- Zaki, A.H.; Zahid, M.T.; Haiying, B. Bioactive compounds of the culinary-medicinal mushroom Leucocalocybe mongolica (Agaricomycetes): Pharmacological and therapeutic applications-A review. Int. J. Med. Mushrooms 2022, 24, 19–33. [Google Scholar] [CrossRef] [PubMed]
- Maser, E.; Lanišnik Rižner, T. Steroids and microorganisms. J. Steroid. Biochem. Mol. Biol. 2012, 129, 1–3. [Google Scholar] [CrossRef]
- El-Baba, C.; Baassiri, A.; Kiriako, G.; Dia, B.; Fadlallah, S.; Moodad, S.; Darwiche, N. Terpenoids’ anti-cancer effects: Focus on autophagy. Apoptosis 2021, 26, 491–511. [Google Scholar] [CrossRef]
- Huang, M.; Lu, J.J.; Huang, M.Q.; Bao, J.L.; Chen, X.P.; Wang, Y.T. Terpenoids: Natural products for cancer therapy. Expert. Opin. Investig. Drugs 2012, 21, 1801–1818. [Google Scholar] [CrossRef] [PubMed]
- Luo, H.; Vong, C.T.; Chen, H.; Gao, Y.; Lyu, P.; Qiu, L.; Zhao, M.; Liu, Q.; Zehua, C.; Zou, Y.; et al. Naturally occurring anticancer compounds: Shining from Chinese herbal medicine. Chin. Med. 2019, 14, 48. [Google Scholar] [CrossRef]
- Ju, S.; Seo, J.Y.; Lee, S.K.; Oh, J.; Kim, J.S. Oral administration of hydrolyzed red ginseng extract improves learning and memory capability of scopolamine-treated C57BL/6J mice via upregulation of Nrf2-mediated antioxidant mechanism. J. Ginseng. Res. 2021, 45, 108–118. [Google Scholar] [CrossRef]
- Tu, T.H.T.; Sharma, N.; Shin, E.J.; Tran, H.Q.; Lee, Y.J.; Jeong, J.H.; Jeong, J.H.; Nah, S.Y.; Tran, H.Y.P.; Byun, J.K.; et al. Ginsenoside Re protects trimethyltin-induced neurotoxicity via activation of IL-6-mediated phosphoinositol 3-kinase/Akt signaling in mice. Neurochem. Res. 2017, 42, 3125–3139. [Google Scholar] [CrossRef]
- Jiang, J.L.; Liang, J.; Yang, Y.Y.; Liu, S.K. Research progress on pharmacological and toxicological effects of Siraitia grosvenori. Mod. Prev. Med. 2020, 47, 2246–2248+2262. [Google Scholar]
- Schmucker, D.L. Age-related changes in liver structure and function: Implications for disease? Exp. Gerontol. 2005, 40, 650–659. [Google Scholar] [CrossRef]
- Shen, X.; Dong, X.; Han, Y.; Li, Y.; Ding, S.; Zhang, H.; Sun, Z.; Yin, Y.; Li, W.; Li, W. Ginsenoside Rg1 ameliorates glomerular fibrosis during kidney aging by inhibiting NOX4 and NLRP3 inflammasome activation in SAMP8 mice. Int. Immunopharmacol. 2020, 82, 106339. [Google Scholar] [CrossRef] [PubMed]
- Chen, Y.; Ding, S.; Zhang, H.; Sun, Z.; Shen, X.; Sun, L.; Yin, Y.; Qun, S.; Li, W. Protective effects of ginsenoside Rg1 on neuronal senescence due to inhibition of NOX2 and NLRP1 inflammasome activation in SAMP8 mice. J. Funct. Foods 2020, 65, 103713. [Google Scholar] [CrossRef]
- Phulara, S.C.; Pandey, S.; Jha, A.; Chauhan, P.S.; Gupta, P.; Shukla, V. Hemiterpene compound, 3,3-dimethylallyl alcohol promotes longevity and neuroprotection in Caenorhabditis elegans. GeroScience 2021, 43, 791–807. [Google Scholar] [CrossRef]
- Omari, Z.; Kazunori, S.; Sabti, M.; Bejaoui, M.; Hafidi, A.; Gadhi, C.; Isoda, H. Dietary administration of cumin-derived cuminaldehyde induce neuroprotective and learning and memory enhancement effects to aging mice. Aging 2021, 13, 1671–1685. [Google Scholar] [CrossRef] [PubMed]
- Chen, Q.; Zhang, Q.; Amrouche, A.T.; Huang, W.; Lu, B. Asperuloside, the bioactive compound in the edible Eucommia ulmoides male flower, delays muscle aging by daf-16 mediated improvement in mitochondrial dysfunction. Food. Funct. 2023, 14, 5562–5575. [Google Scholar] [CrossRef]
- Kumar, K.J.S.; Vani, M.G.; Wang, S.Y. Limonene protects human skin keratinocytes against UVB-induced photodamage and photoaging by activating the Nrf2-dependent antioxidant defense system. Environ. Toxicol. 2022, 37, 2897–2909. [Google Scholar] [CrossRef]
- El-Far, A.H.; Mohamed, H.H.; Elsabagh, D.A.; Mohamed, S.A.; Noreldin, A.E.; Al Jaouni, S.K.; Alsenosy, A.A. Eugenol and carvacrol attenuate brain D-galactose-induced aging-related oxidative alterations in rats. Environ. Sci. Pollut. R. 2022, 29, 47436–47447. [Google Scholar] [CrossRef]
- Mu, H.Y.; Gao, Y.H.; Cao, G.C.; Jiang, J.Y.; Wang, H.B.; Zhao, W.M. Dihydro-β-agarofuran-type sesquiterpenoids from the seeds of Celastrus virens with lifespan-extending effect on the nematode Caenorhabditis elegans. Fitoterapia 2022, 158, 105165. [Google Scholar] [CrossRef]
- Mohankumar, A.; Kalaiselvi, D.; Thiruppathi, G.; Muthusaravanan, S.; Nivitha, S.; Levenson, C.; Tawata, S.; Sundararaj, P. α- and β-Santalols delay aging in Caenorhabditis elegans via preventing oxidative stress and protein aggregation. ACS. Omega 2020, 5, 32641–32654. [Google Scholar] [CrossRef]
- Chen, M.; Wen, H.; Zhou, S.; Yan, X.; Li, H. Patchouli alcohol inhibits D-gal induced oxidative stress and ameliorates the quality of aging cartilage via activating the Nrf2/HO-1 pathway in mice. Oxid. Med. Cell. Longev. 2022, 2022, 6821170. [Google Scholar] [CrossRef]
- Tsai, Y.C.; Lin, Y.C.; Huang, C.C.; Villaflores, O.B.; Wu, T.Y.; Huang, S.M.; Chin, T.Y. Hericium erinaceus mycelium and its isolated compound, erinacine A, ameliorate high-fat high-sucrose diet-induced metabolic dysfunction and spatial learning deficits in aging mice. J. Med. Food. 2019, 22, 469–478. [Google Scholar] [CrossRef]
- Lin, C.; Zhang, X.; Su, Z.; Xiao, J.; Lv, M.; Cao, Y.; Chen, Y. Carnosol improved lifespan and healthspan by promoting antioxidant capacity in Caenorhabditis elegans. Oxid. Med. Cell. Longev. 2019, 2019, 5958043. [Google Scholar] [CrossRef] [PubMed]
- Oliva, C.A.; Rivera, D.S.; Torres, A.K.; Lindsay, C.B.; Tapia-Rojas, C.; Bozinovic, F.; Inestrosa, N.C. Age-dependent behavioral and synaptic dysfunction impairment are improved with long-term andrographolide administration in long-lived female degus (Octodon degus). Int. J. Mol. Sci. 2023, 24, 1105. [Google Scholar] [CrossRef]
- Yang, Q.; Lin, J.; Zhang, H.; Liu, Y.; Kan, M.; Xiu, Z.; Chen, X.; Lan, X.; Li, X.; Shi, X.; et al. Ginsenoside compound K regulates amyloid β via the Nrf2/Keap1 signaling pathway in mice with scopolamine hydrobromide-induced memory impairments. J. Mol. Neurosci. 2019, 67, 62–71. [Google Scholar] [CrossRef]
- Zong, W.; Zeng, X.; Chen, S.; Chen, L.; Zhou, L.; Wang, X.; Gao, Q.; Zeng, G.; Hu, K.; Ou-Yang, D.S. Ginsenoside compound K attenuates cognitive deficits in vascular dementia rats by reducing the Aβ deposition. J. Pharmacol. Sci. 2019, 139, 223–230. [Google Scholar] [CrossRef]
- Kim, E.; Kim, N.; Yoo, S.; Hong, Y.H.; Han, S.Y.; Jeong, S.; Jeong, D.; Kim, J.H.; Cho, J.; Park, J. The skin protective effects of compound K, a metabolite of ginsenoside Rb1 from Panax ginseng. J. Ginseng Res. 2017, 42, 218–224. [Google Scholar] [CrossRef] [PubMed]
- Zhou, Y.; Wang, Y.P.; He, Y.H.; Ding, J.C. Ginsenoside Rg1 performs anti-aging functions by suppressing mitochondrial pathway-mediated apoptosis and activating sirtuin 3 (SIRT3)/superoxide dismutase 2 (SOD2) pathway in Sca-1⁺ HSC/HPC cells of an aging rat model. Med. Sci. Monit. 2020, 26, e920666. [Google Scholar] [CrossRef]
- Yu, S.; Xia, H.; Guo, Y.; Qian, X.; Zou, X.; Yang, H.; Yin, M.; Liu, H. Ginsenoside Rb1 retards aging process by regulating cell cycle, apoptotic pathway and metabolism of aging mice. J. Ethnopharmacol. 2020, 255, 112746. [Google Scholar] [CrossRef] [PubMed]
- Lim, T.G.; Jeon, A.J.; Yoon, J.H.; Song, D.; Kim, J.E.; Kwon, J.Y.; Kim, J.R.; Kang, N.J.; Park, J.S.; Yeom, M.H.; et al. 20-O-β-D-glucopyranosyl-20(S)-protopanaxadiol, a metabolite of ginsenoside Rb1, enhances the production of hyaluronic acid through the activation of ERK and Akt mediated by Src tyrosin kinase in human keratinocytes. Int. J. Mol. Med. 2015, 35, 1388–1394. [Google Scholar] [CrossRef]
- Xu, Y.; Yuan, H.; Luo, Y.; Zhao, Y.J.; Xiao, J.H. Ganoderic acid D protects human amniotic mesenchymal stem cells against oxidative stress-induced senescence through the PERK/NRF2 signaling pathway. Oxid. Med. Cell. Longev. 2020, 2020, 8291413. [Google Scholar] [CrossRef]
- Yuan, H.; Xu, Y.; Luo, Y.; Zhang, J.R.; Zhu, X.X.; Xiao, J.H. Ganoderic acid D prevents oxidative stress-induced senescence by targeting 14-3-3ε to activate CaM/CaMKII/NRF2 signaling pathway in mesenchymal stem cells. Aging Cell 2022, 21, e13686. [Google Scholar] [CrossRef]
- Montilla, M.P.; Agil, A.; Navarro, M.C.; Jiménez, M.I.; García-Granados, A.; Parra, A.; Cabo, M.M. Antioxidant activity of maslinic acid, a triterpene derivative obtained from Olea europaea. Planta. Medica 2003, 69, 472–474. [Google Scholar]
- Bakhtiari, N.; Hosseinkhani, S.; Soleimani, M.; Hemmati, R.; Noori-Zadeh, A.; Javan, M.; Tashakor, A. Short-term ursolic acid promotes skeletal muscle rejuvenation through enhancing of SIRT1 expression and satellite cells proliferation. Biomed. Pharmacother. 2016, 78, 185–196. [Google Scholar] [CrossRef] [PubMed]
- Gharibi, S.; Bakhtiari, N.; Elham-Moslemee-Jalalvand; Bakhtiari, F. Ursolic acid mediates hepatic protection through enhancing of anti-aging biomarkers. Curr Aging Sci. 2018, 11, 16–23. [Google Scholar] [CrossRef] [PubMed]
- Chen, C.; Ni, Y.; Jiang, B.; Yan, S.; Xu, B.; Fan, B.; Huang, H.; Chen, G. Anti-aging derivatives of cycloastragenol produced by biotransformation. Nat. Prod. Res. 2021, 35, 2685–2690. [Google Scholar] [CrossRef] [PubMed]
- Valenzuela, H.F.; Fuller, T.; Edwards, J.; Finger, D.; Molgora, B. Cycloastragenol extends T cell proliferation by increasing telomerase activity. J. Immunol. 2009, 18, 9030. [Google Scholar] [CrossRef]
- Choi, Y.H. Activation of the Nrf2/HO-1 signaling pathway contributes to the protective effects of platycodin D against oxidative stress-induced DNA damage and apoptosis in C2C12 myoblasts. Gen. Physiol. Biophys. 2020, 39, 519–530. [Google Scholar] [CrossRef]
- Nguyen, B.T.; Shin, E.J.; Jeong, J.H.; Sharma, N.; Nah, S.Y.; Ko, S.K.; Byun, J.K.; Lee, Y.; Lei, X.G.; Kim, D.J.; et al. Ginsenoside Re attenuates memory impairments in aged Klotho deficient mice via interactive modulations of angiotensin II AT1 receptor, Nrf2 and GPx-1 gene. Free. Radic. Biol. Med. 2022, 189, 2–19. [Google Scholar] [CrossRef]
- Li, Y.; Zhang, D.; Li, L.; Han, Y.; Dong, X.; Yang, L.; Li, X.; Li, W.; Li, W. Ginsenoside Rg1 ameliorates aging-induced liver fibrosis by inhibiting the NOX4/NLRP3 inflammasome in SAMP8 mice. Mol. Med. Rep. 2021, 24, 801. [Google Scholar] [CrossRef]
- Zhong, S.J.; Wang, L.; Gu, R.Z.; Zhang, W.H.; Lan, R.; Qin, X.Y. Ginsenoside Rg1 ameliorates the cognitive deficits in D-galactose and AlCl3-induced aging mice by restoring FGF2-Akt and BDNF-TrkB signaling axis to inhibit apoptosis. Int. J. Med. Sci. 2020, 17, 1048–1055. [Google Scholar] [CrossRef]
- Lasekan, O. Identification of the aroma compounds in Vitex doniana sweet: Free and bound odorants. Chem. Cent. J. 2017, 11, 19. [Google Scholar] [CrossRef] [PubMed]
- Sharifi-Rad, M.; Varoni, E.M.; Iriti, M.; Martorell, M.; Setzer, W.N.; Del Mar Contreras, M.; Salehi, B.; Soltani-Nejad, A.; Rajabi, S.; Tajbakhsh, M.; et al. Carvacrol and human health: A comprehensive review. Phytother. Res. 2018, 32, 1675–1687. [Google Scholar] [CrossRef] [PubMed]
- Fu, Y.; Zhao, W. Polyesterified sesquiterpenoids from the seeds of Celastrus paniculatus as lifespan-extending agents for the nematode Caenorhabditis elegans. J. Nat. Prod. 2020, 83, 505–515. [Google Scholar] [CrossRef] [PubMed]
- Zhu, J.; Mu, X.; Zeng, J.; Xu, C.; Liu, J.; Zhang, M.; Li, C.; Chen, J.; Li, T.; Wang, Y. Ginsenoside Rg1 prevents cognitive impairment and hippocampus senescence in a rat model of D-galactose-induced aging. PLoS ONE 2014, 9, e101291. [Google Scholar] [CrossRef]
- Bakhtiari, N.; Hosseinkhani, S.; Tashakor, A.; Hemmati, R. Ursolic acid ameliorates aging-metabolic phenotype through promoting of skeletal muscle rejuvenation. Med. Hypotheses 2015, 85, 1–6. [Google Scholar] [CrossRef]
- Bjørklund, G.; Shanaida, M.; Lysiuk, R.; Butnariu, M.; Peana, M.; Sarac, I.; Strus, O.; Smetanina, K.; Chirumbolo, S. Natural compounds and products from an anti-aging perspective. Molecules 2022, 27, 7084. [Google Scholar] [CrossRef]
- Pisoschi, A.M.; Pop, A.; Iordache, F.; Stanca, L.; Geicu, O.I.; Bilteanu, L.; Serban, A.I. Antioxidant, anti-inflammatory and immunomodulatory roles of vitamins in COVID-19 therapy. Eur. J. Med. Chem. 2022, 232, 114175. [Google Scholar] [CrossRef]
- Ashor, A.W.; Brown, R.; Keenan, P.D.; Willis, N.D.; Siervo, M.; Mathers, J.C. Limited evidence for a beneficial effect of vitamin C supplementation on biomarkers of cardiovascular diseases: An umbrella review of systematic reviews and meta-analyses. Nutr. Res. 2019, 61, 1–12. [Google Scholar] [CrossRef]
- Zou, Y.X.; Ruan, M.H.; Luan, J.; Feng, X.; Chen, S.; Chu, Z.Y. Anti-aging effect of riboflavin via endogenous antioxidant in fruit fly Drosophila Melanogaster. J. Nutr. Health. Aging 2017, 21, 314–319. [Google Scholar] [CrossRef]
- Kim, H.M.; Byun, K.A.; Oh, S.; Yang, J.Y.; Park, H.J.; Chung, M.S.; Son, K.H.; Byun, K. A mixture of topical forms of polydeoxyribonucleotide, vitamin C, and niacinamide attenuated skin pigmentation and increased skin elasticity by modulating nuclear factor erythroid 2-like 2. Molecules 2022, 27, 1276. [Google Scholar] [CrossRef] [PubMed]
- Martín-Martínez, A.; Sánchez-Marzo, N.; Martínez-Casanova, D.; Abarquero-Cerezo, M.; Herranz-López, M.; Barrajón-Catalán, E.; Matabuena-Yzaguirre, M. High global antioxidant protection and stimulation of the collagen synthesis of new anti-aging product containing an optimized active mix. J. Cosmet. Dermatol. 2022, 21, 3993–4000. [Google Scholar] [CrossRef] [PubMed]
- Liu, D.; Gu, Y.; Pang, Q.; Han, Q.; Li, A.; Wu, W.; Zhang, X.; Shi, Q.; Zhu, L.; Yu, H.; et al. Vitamin C inhibits lipid deposition through GSK-3β/mTOR signaling in the liver of zebrafish. Fish. Physiol. Biochem. 2020, 46, 383–394. [Google Scholar] [CrossRef]
- La Fata, G.; van Vliet, N.; Barnhoorn, S.; Brandt, R.M.C.; Etheve, S.; Chenal, E.; Grunenwald, C.; Seifert, N.; Weber, P.; Hoeijmakers, J.H.J.; et al. Vitamin E supplementation reduces cellular loss in the brain of a premature aging mouse model. J. Prev. Alzheimers. Dis. 2017, 4, 226–235. [Google Scholar] [PubMed]
- Liu, X.; Yang, Q.; Li, H.; Lan, X.; Kan, M.; Lin, J.; Wang, J.; Zhang, Z.; Ming, S.; Li, Z.; et al. The anti-aging effect of velvet antler polypeptide is dependent on modulation of the gut microbiota and regulation of the PPARα/APOE4 pathway. J. Integr. Neurosci. 2021, 20, 573–583. [Google Scholar]
- Amevor, F.K.; Cui, Z.; Du, X.; Ning, Z.; Deng, X.; Xu, D.; Shu, G.; Wu, Y.; Cao, X.; Shuo, W.; et al. Supplementation of dietary quercetin and vitamin E promotes the intestinal structure and immune barrier integrity in aged breeder hens. Front. Immunol. 2022, 13, 860889. [Google Scholar] [CrossRef] [PubMed]
- Ambrożewicz, E.; Muszyńska, M.; Tokajuk, G.; Grynkiewicz, G.; Žarković, N.; Skrzydlewska, E. Beneficial effects of vitamins K and D3 on redox balance of human osteoblasts cultured with hydroxyapatite-based biomaterials. Cells 2019, 8, 325. [Google Scholar] [CrossRef] [PubMed]
- Qu, Z.; Zhang, L.; Huang, W.; Zheng, S. Vitamin K2 enhances fat degradation to improve the survival of C. elegans. Front. Nutr. 2022, 9, 858481. [Google Scholar] [CrossRef]
- Pham, V.T.; Dold, S.; Rehman, A.; Bird, J.K.; Steinert, R.E. Vitamins, the gut microbiome and gastrointestinal health in humans. Nutr. Res. 2021, 95, 35–53. [Google Scholar] [CrossRef]
- Dym, O.; Eisenberg, D. Sequence-structure analysis of FAD-containing proteins. Protein Sci. 2001, 10, 1712–1728. [Google Scholar] [CrossRef] [PubMed]
- Cardoso, D.R.; Libardi, S.H.; Skibsted, L.H. Riboflavin as a photosensitizer. Effects on human health and food quality. Food Funct. 2012, 3, 487–502. [Google Scholar] [CrossRef] [PubMed]
- Buehler, B.A. Vitamin B2: Riboflavin. J. Evid. Based Complement. Altern. Med. 2011, 16, 88–90. [Google Scholar] [CrossRef]
- Naveed, S.; Sajid, S. Degradation in pharmaceutical creams: Ascorbic acid demonstrating phenomenon. J. Bioequivalence. Bioavailab. 2016, 8, 80–83. [Google Scholar] [CrossRef]
- Mumtaz, S.; Ali, S.; Tahir, H.M.; Kazmi, S.A.R.; Shakir, H.A.; Mughal, T.A.; Mumtaz, S.; Summer, M.; Farooq, M.A. Aging and its treatment with vitamin C: A comprehensive mechanistic review. Mol. Biol. Rep. 2021, 48, 8141–8153. [Google Scholar] [CrossRef]
- Guida, J.L.; Agurs-Collins, T.; Ahles, T.A.; Campisi, J.; William Dale, W.; Demark-Wahnefried, W.; Dietrich, J.; Fuldner, R.; Gallicchio, L.; Green, P.A.; et al. Strategies to prevent or remediate cancer and treatment-related aging. J. Nat. Cancer. Inst. 2021, 113, 112–122. [Google Scholar]
- Markiewicz-Tomczyk, A.; Budzisz, E.; Erkiert-Polguj, A. Clinical evaluation of anti-aging effects of combined therapy-Azelaic acid, phytic acid, and vitamin C applied layer by layer in females with Fitzpatrick skin types II and III. J. Cosmet. Dermatol. 2022, 21, 6830–6839. [Google Scholar] [CrossRef]
- Goldberg, D.J.; Robinson, D.M.; Granger, C. Clinical evidence of the efficacy and safety of a new 3-in-1 anti-aging topical night serum-in-oil containing melatonin, bakuchiol, and ascorbyl tetraisopalmitate: 103 Females treated from 28 to 84 days. J. Cosmet. Dermatol. 2019, 18, 806–814. [Google Scholar] [CrossRef]
- Akulinina, I.; Stefanaki, I.; Pavlíčková, E.; Maiolino, M.; Hajduk, S.; Sápy, M.; Mertin, B.; Rijo, H.; Tekeli, Ö.; Valois, A.; et al. Topical formulation containing peptides and vitamin C in ampoules improves skin aging signs: Results of a large, international, observational study. J. Cosmet. Dermatol. 2022, 21, 3910–3916. [Google Scholar] [CrossRef]
- Rattanawiwatpong, P.; Wanitphakdeedecha, R.; Bumrungpert, A.; Maiprasert, M. Anti-aging and brightening effects of a topical treatment containing vitamin C, vitamin E, and raspberry leaf cell culture extract: A split-face, randomized controlled trial. J. Cosmet. Dermatol. 2020, 19, 671–676. [Google Scholar] [CrossRef]
- Handler, M.; Adams-Woodford, A.; Ayres, P.; Giancola, G.; Diaz, I. Facial aging improvement case study using a novel combination of retinol, niacinamide, and Terminalia Chebula. J. Drugs. Dermatol. 2022, 21, 784–788. [Google Scholar] [PubMed]
- Jang, S.I.; Jung, Y.C.; Suk, J.; Lee, S.; Han, J.; Suh, B.F.; Kim, E. A long term study of the difference in efficacy and effect rate of various concentrations of retinol (1500–6600 IU) in middle aged women. Arch. Dermatol. Res. 2023, 315, 1323–1332. [Google Scholar] [CrossRef]
- Abed, K.; Foucher, A.; Bernard, D.; Tancrède-Bohin, E.; Cavusoglu, N. One-year longitudinal study of the stratum corneum proteome of retinol and all-trans-retinoic acid treated human skin: An orchestrated molecular event. Sci. Rep. 2023, 13, 11196. [Google Scholar] [CrossRef] [PubMed]
- Kamal-Eldin, A.; Appelqvist, L.A. The chemistry and antioxidant properties of tocopherols and tocotrienols. Lipids 1996, 31, 671–701. [Google Scholar] [PubMed]
- Rigotti, A. Absorption, transport, and tissue delivery of vitamin E. Mol. Aspects. Med. 2007, 28, 423–436. [Google Scholar] [PubMed]
- Brigelius-Flohe, R.; Traber, M.G. Vitamin E: Function and metabolism. FASEB J. 1999, 13, 1145–1155. [Google Scholar] [CrossRef]
- Mocchegiani, E.; Costarelli, L.; Giacconi, R.; Malavolta, M.; Basso, A.; Piacenza, F.; Ostan, R.; Cevenini, E.; Gonos, E.S.; Franceschi, C.; et al. Vitamin E-gene interactions in aging and inflammatory age-related diseases: Implications for treatment. A systematic review. Ageing Res. Rev. 2014, 14, 81–101. [Google Scholar]
- Takahashi, T.; Nakaso, K.; Horikoshi, Y.; Hanaki, T.; Yamakawa, M.; Nakasone, M.; Kitagawa, Y.; Koike, T.; Matsura, T. Rice bran dietary supplementation improves neurological symptoms and loss of purkinje cells in vitamin E-deficient mice. Yonago. Acta. Med. 2016, 59, 188–195. [Google Scholar]
- Wang, L.; Chen, Q.; Zhuang, S.; Wen, Y.; Cheng, W.; Zeng, Z.; Jiang, T.; Tang, C. Effect of Anoectochilus roxburghii flavonoids extract on H2O2—Induced oxidative stress in LO2 cells and D-gal induced aging mice model. J. Ethnopharmacol. 2020, 254, 112670. [Google Scholar]
- Na Takuathung, M.; Klinjan, P.; Sakuludomkan, W.; Dukaew, N.; Inpan, R.; Kongta, R.; Chaiyana, W.; Teekachunhatean, S.; Koonrungsesomboon, N. Efficacy and safety of the genistein nutraceutical product containing vitamin E, vitamin B3, and ceramide on skin health in postmenopausal women: A randomized, double-blind, placebo-controlled clinical trial. J. Clin. Med. 2023, 12, 1326. [Google Scholar]
- Farris, P.; Yatskayer, M.; Chen, N.; Krol, Y.; Oresajo, C. Evaluation of efficacy and tolerance of a nighttime topical antioxidant containing resveratrol, baicalin, and vitamin e for treatment of mild to moderately photodamaged skin. J. Drugs. Dermatol. 2014, 13, 1467–1472. [Google Scholar] [PubMed]
- Fujitaka, Y.; Hamada, H.; Uesugi, D.; Kuboki, A.; Shimoda, K.; Iwaki, T.; Kiriake, Y.; Saikawa, T. Synthesis of daidzein glycosides, α-tocopherol glycosides, hesperetin glycosides by bioconversion and their potential for anti-allergic functional-foods and cosmetics. Molecules 2019, 24, 2975. [Google Scholar] [CrossRef] [PubMed]
- Popa, D.S.; Bigman, G.; Rusu, M.E. The role of vitamin K in humans: Implication in aging and age-associated diseases. Antioxidants 2021, 10, 566. [Google Scholar] [CrossRef] [PubMed]
- Simes, D.C.; Viegas, C.S.B.; Araújo, N.; Marreiros, C. Vitamin K as a powerful micronutrient in aging and age-related diseases: Pros and cons from clinical studies. Int. J. Mol. Sci. 2019, 20, 4150. [Google Scholar] [CrossRef]
- Simes, D.C.; Viegas, C.S.B.; Araújo, N.; Marreiros, C. Vitamin K as a diet supplement with impact in human health: Current evidence in age-related diseases. Nutrients 2020, 12, 138. [Google Scholar] [CrossRef]
- Booth, S.L.; Shea, M.K.; Barger, K.; Leurgans, S.E.; James, B.D.; Holland, T.M.; Agarwal, P.; Fu, X.; Wang, J.; Matuszek, G.; et al. Association of vitamin K with cognitive decline and neuropathology in community-dwelling older persons. Alzheimers Dement. 2022, 8, e12255. [Google Scholar] [CrossRef]
- van Ballegooijen, A.J.; van Putten, S.R.; Visser, M.; Beulens, J.W.; Hoogendijk, E.O. Vitamin K status and physical decline in older adults-the longitudinal aging study amsterdam. Maturitas 2018, 113, 73–79. [Google Scholar] [CrossRef]
- Shea, M.K.; Kritchevsky, S.B.; Loeser, R.F.; Booth, S.L. Vitamin K status and mobility limitation and disability in older adults: The health, aging, and body composition study. J. Gerontol. A. Biol. Sci. Med. Sci. 2020, 75, 792–797. [Google Scholar]
- Doisy, E.A.; Binkley, S.B.; Thayer, S.A.; Mc Kee, R.W. Vitamin K. Science 1940, 91, 58–62. [Google Scholar] [CrossRef]
- Nelsestuen, G.L.; Zytkovicz, T.H.; Howard, J.B. The mode of action of vitamin K. Identification of gamma-carboxyglutamic acid as a component of prothrombin. J. Biol. Chem. 1974, 249, 6347–6350. [Google Scholar] [CrossRef]
- Azuma, K.; Inoue, S. Multiple modes of vitamin K actions in aging-related musculoskeletal disorders. Int. J. Mol. Sci. 2019, 20, 2844. [Google Scholar] [CrossRef]
- Sim, M.; Lewis, J.R.; Prince, R.L.; Levinger, I.; Brennan-Speranza, T.C.; Palmer, C.; Bondonno, C.P.; Bondonno, N.P.; Devine, A.; Ward, N.C.; et al. The effects of vitamin K-rich green leafy vegetables on bone metabolism: A 4-week randomised controlled trial in middle-aged and older individuals. Bone Rep. 2020, 12, 100274. [Google Scholar] [CrossRef]
- Camacho-Barcia, L.; García-Gavilán, J.; Martínez-González, M.Á.; Fernández-Aranda, F.; Galié, S.; Corella, D.; Cuenca-Royo, A.; Romaguera, D.; Vioque, J.; Alonso-Gómez, A.M.; et al. Vitamin K dietary intake is associated with cognitive function in an older adult Mediterranean population. Age Ageing 2022, 51, afab246. [Google Scholar] [CrossRef]
- Shea, M.K.; Wang, J.; Barger, K.; Weiner, D.E.; Booth, S.L.; Seliger, S.L.; Anderson, A.H.; Deo, R.; Feldman, H.I.; Go, A.S.; et al. Cric study investigators. Vitamin K status and cognitive function in adults with chronic kidney disease: The chronic renal insufficiency cohort. Curr. Dev. Nutr. 2022, 6, nzac111. [Google Scholar] [CrossRef]
- Giordano, S.; Darley-Usmar, V.; Zhang, J.H. Autophagy as an essential cellular antioxidant pathway in neurodegenerative disease. Redox. Biol. 2013, 2, 82–90. [Google Scholar] [CrossRef]
- Sykiotis, G.P.; Bohmann, D. Keap1/Nrf2 signaling regulates oxidative stress tolerance and lifespan in Drosophila. Dev. Cell. 2008, 14, 76–85. [Google Scholar] [CrossRef]
- Magesh, S.; Chen, Y.; Hu, L. Small molecule modulators of Keap1-Nrf2-ARE pathway as potential preventive and therapeutic agents. Med. Res. Rev. 2012, 32, 687–726. [Google Scholar] [CrossRef] [PubMed]
- Mu, S.; Yang, W.; Huang, G. Antioxidant activities and mechanisms of polysaccharides. Chem. Biol. Drug Des. 2021, 97, 628–632. [Google Scholar] [CrossRef]
- Hsieh, T.C.; Lu, X.; Wang, Z.; Wu, J.M. Induction of quinone reductase NQO1 by resveratrol in human K562 cells involves the antioxidant response element ARE and is accompanied by nuclear translocation of transcription factor Nrf2. Med. Chem. 2006, 2, 275–285. [Google Scholar] [PubMed]
- Szewczyk, K.; Pietrzak, W.; Klimek, K.; Miazga-Karska, M.; Firlej, A.; Flisiński, M.; Grzywa-Celińska, A. Flavonoid and phenolic acids content and in vitro study of the potential anti-aging properties of Eutrema japonicum (Miq.) koidz cultivated in wasabi farm Poland. Int. J. Mol. Sci. 2021, 22, 6219. [Google Scholar] [CrossRef] [PubMed]
- Mu, X.; Zhang, Y.; Li, J.; Xia, J.; Chen, X.; Jing, P.; Song, X.; Wang, L.; Wang, Y. Angelica Sinensis polysaccharide prevents hematopoietic stem cells senescence in D-galactose-induced aging mouse model. Stem. Cells. Int. 2017, 2017, 3508907. [Google Scholar] [CrossRef]
- Rodier, F.; Campisi, J. Four faces of cellular senescence. J. Cell Biol. 2011, 192, 547–556. [Google Scholar] [CrossRef]
- Ruan, Y.; Dong, C.; Patel, J.; Duan, C.; Wang, X.; Wu, X.; Cao, Y.; Pu, L.; Lu, D.; Shen, T.; et al. SIRT1 suppresses doxorubicin-induced cardiotoxicity by regulating the oxidative stress and p38MAPK pathways. Cell Physiol. Biochem. 2015, 35, 1116–1124. [Google Scholar] [CrossRef]
- Ou, H.L.; Schumacher, B. DNA damage responses and p53 in the aging process. Blood 2018, 131, 488–495. [Google Scholar] [CrossRef] [PubMed]
- Dutto, I.; Tillhon, M.; Cazzalini, O.; Stivala, L.A.; Prosperi, E. Biology of the cell cycle inhibitor p21 (CDKN1A): Molecular mechanisms and relevance in chemical toxicology. Arch. Toxicol. 2015, 89, 155–178. [Google Scholar] [CrossRef]
- Chhabra, G.; Garvey, D.R.; Singh, C.K.; Mintie, C.A.; Ahmad, N. Effects and mechanism of nicotinamide against UVA- and/or UVB-mediated DNA damages in normal melanocytes. Photochem. Photobiol. 2019, 95, 331–337. [Google Scholar] [CrossRef]
- Lebiedzinska, M.; Karkucinska-Wieckowska, A.; Giorgi, C.; Karczmarewicz, E.; Pronicka, E.; Pinton, P.; Duszynski, J.; Pronicki, M.; Wieckowski, M.R. Oxidative stress-dependent p66Shc phosphorylation in skin fibroblasts of children with mitochondrial disorders. Biochim. Biophys. Acta 2010, 1797, 952–960. [Google Scholar] [CrossRef]
- Arany, I.; Hall, S.; Reed, D.K.; Dixit, M. The pro-oxidant gene p66Shc increases nicotine exposure-induced lipotoxic oxidative stress in renal proximal tubule cells. Mol. Med. Rep. 2016, 14, 2771–2777. [Google Scholar] [CrossRef] [PubMed]
- Perrini, S.; Tortosa, F.; Natalicchio, A.; Pacelli, C.; Cignarelli, A.; Palmieri, V.O.; Caccioppoli, C.; De Stefano, F.; Porro, S.; Leonardini, A. The p66Shc protein controls redox signaling and oxidation-dependent DNA damage in human liver cells. Am. J. Physiol. Gastrointest. Liver. Physiol. 2015, 309, G826–G840. [Google Scholar] [CrossRef] [PubMed]
- Roitenberg, N.; Bejerano-Sagie, M.; Boocholez, H.; Moll, L.; Marques, F.C.; Golodetzki, L.; Nevo, Y.; Elami, T.; Cohen, E. Modulation of caveolae by insulin/IGF-1 signaling regulates aging of Caenorhabditis elegans. Embo Rep. 2018, 19, e45673. [Google Scholar] [CrossRef]
- Murphy, C.T.; McCarroll, S.A.; Bargmann, C.I.; Fraser, A.; Kamath, R.S.; Ahringer, J.; Li, H.; Kenyon, C. Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans. Nature 2003, 424, 277–283. [Google Scholar] [CrossRef] [PubMed]
- Sen, I.; Zhou, X.; Chernobrovkin, A.; Puerta-Cavanzo, N.; Kanno, T.; Salignon, J.; Stoehr, A.; Lin, X.; Baskaner, B.; Brandenburg, S.; et al. DAF-16/FOXO requires protein phosphatase 4 to initiate transcription of stress resistance and longevity promoting genes. Nat. Commun. 2020, 11, 138. [Google Scholar] [CrossRef] [PubMed]
- Sun, X.; Chen, W.D.; Wang, Y.D. DAF-16/FOXO transcription factor in aging and longevity. Front. Pharmacol. 2017, 8, 548. [Google Scholar] [CrossRef]
- Zhang, Z.; Gao, T.; Yan, N.; Duan, Z.; Tang, Z.; Zhou, L.; Chen, T.; Feng, S.; Ding, C.; Yuan, S.; et al. Characterization and anti-aging activity of polysaccharides from Akebia trifoliata fruit separated by an aqueous two-phase system. Plant. Foods. Hum. Nutr. 2023, 78, 154–159. [Google Scholar] [CrossRef] [PubMed]
- Busti, S.; Coccetti, P.; Alberghina, L.; Vanoni, M. Glucose signaling-mediated coordination of cell growth and cell cycle in Saccharomyces Cerevisiae. Sensors 2010, 10, 6195–6240. [Google Scholar] [CrossRef] [PubMed]
- Nicastro, R.; Tripodi, F.; Gaggini, M.; Castoldi, A.; Reghellin, V.; Nonnis, S.; Tedeschi, G.; Coccetti, P. Snf1 phosphorylates adenylate cyclase and negatively regulates protein kinase a-dependent transcription in Saccharomyces Cerevisiae. J. Biol. Chem. 2015, 290, 24715–24726. [Google Scholar] [CrossRef]
- Kovacs, E.J.; Palmer, J.L.; Fortin, C.F.; Fulop, T.J.; Goldstein, D.R.; Linton, P.J. Aging and innate immunity in the mouse: Impact of intrinsic and extrinsic factors. Trends. Immunol. 2009, 30, 319–324. [Google Scholar] [CrossRef]
- Budamagunta, V.; Manohar-Sindhu, S.; Yang, Y.; He, Y.; Traktuev, D.O.; Foster, T.C.; Zhou, D. Senescence-associated hyperactivation to inflammatory stimuli in vitro. Aging 2021, 13, 19088–19107. [Google Scholar] [CrossRef]
- Zhang, W.; Hwang, J.; Park, H.B.; Lim, S.M.; Go, S.; Kim, J.; Choi, I.; You, S.; Jin, J.O. Human peripheral blood dendritic cell and T cell activation by Codium fragile polysaccharide. Mar. Drugs 2020, 18, 535. [Google Scholar] [CrossRef]
- Higami, Y.; Shimokawa, I. Apoptosis in the aging process. Cell Tissue. Res. 2000, 301, 125–132. [Google Scholar] [CrossRef]
- Kim, S.; Jazwinski, S.M. The gut microbiota and healthy aging: A mini-review. Gerontology 2018, 64, 513–520. [Google Scholar] [CrossRef] [PubMed]
- Shi, H.; Ge, X.; Ma, X.; Zheng, M.; Cui, X.; Pan, W.; Zheng, P.; Yang, X.; Hu, M.; Hu, T.; et al. A fiber-deprived diet causes cognitive impairment and hippocampal microglia-mediated synaptic loss through the gut microbiota and metabolites. Microbiome 2021, 9, 223. [Google Scholar] [CrossRef] [PubMed]
- Ghosh, T.S.; Rampelli, S.; Jeffery, I.; Santoro, A.; Neto, M.; Capri, M.; Giampieri, E.; Jennings, A.; Candela, M.; Turroni, S.; et al. Mediterranean diet intervention alters the gut microbiome in older people reducing frailty and improving health status: The NU-AGE 1-year dietary intervention across five European countries. Gut 2020, 69, 1218–1228. [Google Scholar] [CrossRef] [PubMed]
- Wang, Q.; Adil, M.Z.; Xie, X.; Zhao, S.; Zhang, J.; Huang, Z. Therapeutic targeting of mitochondria-proteostasis axis by antioxidant polysaccharides in neurodegeneration. Adv. Protein Chem. Struct. Biol. 2023, 136, 385–413. [Google Scholar]
- Deng, R.; Wang, F.; Wang, L.; Xiong, L.; Shen, X.; Song, H. Advances in plant polysaccharides as antiaging agents: Effects and signaling mechanisms. J. Agric. Food. Chem. 2023, 71, 7175–7191. [Google Scholar] [CrossRef]
- Tan, Y.; Yin, L.; Sun, Z.; Shao, S.; Chen, W.; Man, X.; Du, Y.; Chen, Y. Astragalus polysaccharide exerts anti-Parkinson via activating the PI3K/AKT/mTOR pathway to increase cellular autophagy level in vitro. Int. J. Biol. Macromol. 2020, 153, 349–356. [Google Scholar] [CrossRef]
- Yao, T.; Chen, J.M.; Shen, L.E.; Yu, Y.S.; Tang, Z.H.; Zang, G.Q.; Zhang, Y.; Chen, X.H. Astragalus polysaccharide alleviated hepatocyte senescence via autophagy pathway. Kaohsiung. J. Med. Sci. 2022, 38, 457–468. [Google Scholar] [CrossRef]
- Wang, X.; Pang, L.; Zhang, Y.; Xu, J.; Ding, D.; Yang, T.; Zhao, Q.; Wu, F.; Li, F.; Meng, H.; et al. Lycium barbarum polysaccharide promotes nigrostriatal dopamine function by modulating PTEN/AKT/mTOR pathway in a Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) murine model of Parkinson’s disease. Neurochem. Res. 2018, 43, 938–947. [Google Scholar] [CrossRef]
- Ren, Z.L.; Wang, C.D.; Wang, T.; Ding, H.; Zhou, M.; Yang, N.; Chan, P. Ganoderma lucidum extract ameliorates MPTP-induced Parkinsonism and protects dopaminergic neurons from oxidative stress via regulating mitochondrial function, autophagy, and apoptosis. Acta Pharmacol. Sin. 2019, 40, 441–450. [Google Scholar] [CrossRef]
- Xiao, X.T.; He, S.Q.; Wu, N.N.; Lin, X.C.; Zhao, J.; Tian, C. Green tea polyphenols prevent early vascular aging induced by high-fat diet via promoting autophagy in young adult rats. Curr. Med. Sci. 2022, 42, 981–990. [Google Scholar] [CrossRef]
- He, C.L.; Tang, Y.; Wu, J.M.; Long, T.; Yu, L.; Teng, J.F.; Qiu, W.Q.; Pan, R.; Yu, C.L.; Qin, D.L.; et al. Chlorogenic acid delays the progression of Parkinson’s disease via autophagy induction in Caenorhabditis elegans. Nutr. Neurosci. 2023, 26, 11–24. [Google Scholar] [CrossRef]
- Lu, R.; He, Z.; Zhang, W.; Wang, Y.; Cheng, P.; Lv, Z.; Yuan, X.; Guo, F.; You, H.; Chen, A.M.; et al. Oroxin B alleviates osteoarthritis through anti-inflammation and inhibition of PI3K/AKT/mTOR signaling pathway and enhancement of autophagy. Front. Endocrinol. 2022, 13, 1060721. [Google Scholar] [CrossRef]
- Hosoda, R.; Nakashima, R.; Yano, M.; Iwahara, N.; Asakura, S.; Nojima, I.; Saga, Y.; Kunimoto, R.; Horio, Y.; Kuno, A. Resveratrol, a SIRT1 activator, attenuates aging-associated alterations in skeletal muscle and heart in mice. J. Pharmacol. Sci. 2023, 152, 112–122. [Google Scholar] [CrossRef]
- Lin, Y.; Kotakeyama, Y.; Li, J.; Pan, Y.; Matsuura, A.; Ohya, Y.; Yoshida, M.; Xiang, L.; Qi, J. Cucurbitacin B exerts antiaging effects in yeast by regulating autophagy and oxidative stress. Oxid. Med. Cell. Longev. 2019, 2019, 4517091. [Google Scholar] [CrossRef] [PubMed]
- Borghesan, M.; Hoogaars, W.M.H.; Varela-Eirin, M.; Talma, N.; Demaria, M.A. Senescence-centric view of aging: Implications for longevity and disease. Trends. Cell Biol. 2020, 30, 777–791. [Google Scholar] [CrossRef] [PubMed]
- Wang, A.S.; Dreesen, O. Biomarkers of cellular senescence and skin aging. Front. Genet. 2018, 9, 247. [Google Scholar] [CrossRef] [PubMed]
- Boyajian, J.L.; Ghebretatios, M.; Schaly, S.; Islam, P.; Prakash, S. Microbiome and human aging: Probiotic and prebiotic potentials in longevity, skin health and cellular senescence. Nutrients 2021, 13, 4550. [Google Scholar] [CrossRef]
- Attaallah, A.; Lenzi, M.; Marchionni, S.; Bincoletto, G.; Cocchi, V.; Croco, E.; Hrelia, P.; Hrelia, S.; Sell, C.; Lorenzini, A. A prolongevity role for cellular senescence. GeroScience 2020, 42, 867–879. [Google Scholar] [CrossRef]
- Coppé, J.P.; Desprez, P.Y.; Krtolica, A.; Campisi, J. The senescence-associated secretory phenotype: The dark side of tumor suppression. Annu. Rev. Pathol. 2010, 5, 99–118. [Google Scholar] [CrossRef]
- Demaria, M.; Desprez, P.Y.; Campisi, J.; Velarde, M.C. Cell autonomous and non-autonomous effects of senescent cells in the skin. J. Investig. Dermatol. 2015, 135, 1722–1726. [Google Scholar] [CrossRef]
- Lee, J.H.; Yun, C.W.; Hur, J.; Lee, S.H. Fucoidan rescues p-cresol-induced cellular senescence in mesenchymal stem cells via FAK-Akt-TWIST axis. Mar. Drugs 2018, 16, 121. [Google Scholar] [CrossRef] [PubMed]
- Jing, P.; Song, X.; Xiong, L.; Wang, B.; Wang, Y.; Wang, L. Angelica sinensis polysaccharides prevents hematopoietic regression in D-Galactose-induced aging model via attenuation of oxidative stress in hematopoietic microenvironment. Mol. Biol. Rep. 2023, 50, 121–132. [Google Scholar] [CrossRef] [PubMed]
- Novais, E.J.; Tran, V.A.; Johnston, S.N.; Darris, K.R.; Roupas, A.J.; Sessions, G.A.; Shapiro, I.M.; Diekman, B.O.; Risbud, M.V. Long-term treatment with senolytic drugs Dasatinib and Quercetin ameliorates age-dependent intervertebral disc degeneration in mice. Nat. Commun. 2021, 12, 5213. [Google Scholar] [CrossRef] [PubMed]
- Liu, H.M.; Cheng, M.Y.; Xun, M.H.; Zhao, Z.W.; Zhang, Y.; Tang, W.; Cheng, J.; Ni, J.; Wang, W. Possible mechanisms of oxidative stress-induced skin cellular senescence, inflammation, and cancer and the therapeutic potential of plant polyphenols. Int. J. Mol. Sci. 2023, 24, 3755. [Google Scholar] [CrossRef] [PubMed]
- Rivas-Chacón, L.D.M.; Yanes-Díaz, J.; de Lucas, B.; Riestra-Ayora, J.I.; Madrid-García, R.; Sanz-Fernández, R.; Sánchez-Rodríguez, C. Cocoa polyphenol extract inhibits cellular senescence via modulation of SIRT1 and SIRT3 in auditory cells. Nutrients 2023, 15, 544. [Google Scholar] [CrossRef]
- Zhang, Y.; Mao, H.; Li, Y.; Xiong, Y.; Liu, X.; Wang, L.; Chen, Z. β-Cryptoxanthin maintains mitochondrial function by promoting NRF2 nuclear translocation to inhibit oxidative stress-induced senescence in HK-2 cells. Int. J. Mol. Sci. 2023, 24, 3851. [Google Scholar] [CrossRef]
- Chen, L.; Holder, R.; Porter, C.; Shah, Z. Vitamin D3 attenuates doxorubicin-induced senescence of human aortic endothelial cells by upregulation of IL-10 via the pAMPKα/Sirt1/Foxo3a signaling pathway. PLoS ONE 2021, 16, e0252816. [Google Scholar] [CrossRef]
- Odama, M.; Maegawa, E.; Suzuki, K.; Fujii, Y.; Maeda, R.; Murakami, S.; Ito, T. Effects of betulinic acid on the proliferation, cellular senescence, and type 1 interferon-related signaling pathways in human dermal fibroblasts. J. Agric. Food. Chem. 2023, 71, 6935–6943. [Google Scholar] [CrossRef]
- De Lange, T. Shelterin: The protein complex that shapes and safeguards human telomeres. Genes. Dev. 2005, 19, 2100–2110. [Google Scholar] [CrossRef]
- Blackburn, E.H. Switching and signaling at the telomere. Cell 2001, 106, 661–673. [Google Scholar] [CrossRef]
- Allsopp, R.C.; Vaziri, H.; Patterson, C.; Goldstein, S.; Younglai, E.V.; Futcher, A.B.; Greider, C.W.; Harley, C.B. Telomere length predicts replicative capacity of human fibroblasts. Proc. Natl. Acad. Sci. USA 1992, 89, 10114–10118. [Google Scholar] [CrossRef] [PubMed]
- de Jesus, B.B.; Schneeberger, K.; Vera, E.; Tejera, A.; Harley, C.B.; Blasco, M.A. The telomerase activator TA-65 elongates short telomeres and increases health span of adult/old mice without increasing cancer incidence. Aging Cell 2011, 10, 604–621. [Google Scholar] [CrossRef] [PubMed]
- Dow, C.T.; Harley, C.B. Evaluation of an oral telomerase activator for early age-related macular degeneration-A pilot study. Clin. Ophthalmol. 2016, 10, 243–249. [Google Scholar] [CrossRef] [PubMed]
- Jäger, K.; Walter, M. Therapeutic targeting of telomerase. Genes 2016, 7, 39. [Google Scholar] [CrossRef]
- Harley, C.B.; Liu, W.; Blasco, M.; Vera, E.; Andrews, W.H.; Briggs, L.A.; Raffaele, J.M. A natural product telomerase activator as part of a health maintenance program. Rejuvenation Res. 2011, 14, 45–56. [Google Scholar] [CrossRef]
- Wang, J.; Liu, Y.; Xia, Q.; Xia, Q.; Wang, B.; Yang, C.; Liang, J.; Liu, X. Potential roles of telomeres and telomerase in neurodegenerative diseases. Int. J. Biol. Macromol. 2020, 163, 1060–1078. [Google Scholar] [CrossRef]
- Duman, S.; Ekiz, G.; Yılmaz, S.; Yusufoglu, H.; Ballar Kırmızıbayrak, P.; Bedir, E. Telomerase activators from 20(27)-octanor-cycloastragenol via biotransformation by the fungal endophytes. Bioorg. Chem. 2021, 109, 104708. [Google Scholar] [CrossRef]
- Küçüksolak, M.; Yılmaz, S.; Ballar-Kırmızıbayrak, P.; Bedir, E. Potent telomerase activators from a novel sapogenin via biotransformation utilizing Camarosporium laburnicola, an endophytic fungus. Microb. Cell Fact. 2023, 22, 66. [Google Scholar] [CrossRef]
- Cai, Y.; Zhong, Y.D.; Zhang, H.; Lu, P.L.; Liang, Y.Y.; Hu, B.; Wu, H. Association between dietary vitamin C and telomere length: A cross-sectional study. Front. Nutr. 2023, 10, 1025936. [Google Scholar] [CrossRef]
- Pagano, G.; Pahardo, F.V.; Lyakhovich, A.; Tiano, L.; Fittipaldi, M.R.; Toscanesi, M.; Trifuoggi, M. Aging-related disorders and mitochondrial dysfunction: A critical review for prospect mitoprotective strategies based on mitochondrial nutrient mixtures. Int. J. Mol. Sci. 2020, 21, 16. [Google Scholar] [CrossRef]
- Natarajan, V.; Chawla, R.; Mah, T.; Vivekanandan, R.; Tan, S.Y.; Sato, P.Y.; Mallilankaraman, K. Mitochondrial dysfunction in age-related metabolic disorders. Proteomics 2020, 20, 11. [Google Scholar] [CrossRef] [PubMed]
- Lagouge, M.; Argmann, C.; Gerhart-Hines, Z.; Meziane, H.; Lerin, C.; Daussin, F.; Messadeq, N.; Milne, J.; Lambert, P.; Elliott, P.; et al. Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1alpha. Cell 2006, 127, 1109–1122. [Google Scholar] [CrossRef] [PubMed]
Figure 1.
The schematic diagram shows the effects of aging on human health.
Figure 2.
The chemical structures of different types of terpenoids.
Table 1.
Anti-aging effects and modes of action of edible polysaccharides.
| Subclasses of Polysaccharides | Representative Components | Models | Main Indicators of Aging | Modes of Action | Reference |
|---|---|---|---|---|---|
| Plant polysaccharides | Chinese wolfberry Lycium barbarum polysaccharide (LBP) | D. melanogaster | Lifespan; MDA content; CAT and SOD activity; The relative mRNA expression of aging-related genes (mapk, tor and s6k) and longevity genes (hep, mth and rpn11). | LBP exerts anti-aging activity by regulation of age-related genes and signaling pathway. | [31] |
| LBP | C. elegans | In-vitro study: 2,2-diphenyl-1-(2,4,6-trinitrophenyl) hydrazyl (DPPH), hydroxyl, superoxide anion radical scavenging activity assay. In-vivo study: Lifespan; Oxidative-stress resistance; Heat-stress resistance; The relative mRNA levels of hsp-16.2, sod-3, daf-16 and daf-2. | LBP prolongs the lifespan of C. elegans by upregulating the expression of daf-16, sod-3 and hsp-16.2. | [32] | |
| LBP | Aging mice induced by estrogen deficiency | Learning and memory impairment assay; Levels of myeloid differentiation factor 88, NF-κB, TNF-α, IL-6 and IL-1β associated with TLR4/NF-κB signaling pathway. | LBP alleviates estrogen deficiency-induced cognitive impairments by downregulating the factors associated with TLR4/NF-κB signaling pathway. | [33] | |
| LBP | UVB-irradiation-treated HaCaT cells | Cell viability; ROS level; DNA damage; Levels of p-p38, p38, mmp-9, caspase-3 and Nrf2; The relative mRNA expression of Nrf2 target genes (AKR1C2, APOE, GCLC, GCLM, HBEGF, HO-1 and NQO1); SOD activity. | LBP protects against UVB irradiation-induced photodamage partially through activation of Nrf2/ARE pathway and suppression of UVB-induced p38 MAPK pathway. | [34] | |
| LBP | PM2.5-treated HaCaT cells | Cell viability and apoptosis assay; ROS level; MDA content; SOD activity; Mitochondrial damage; Autophagosome level. | LBP protects skin cells from PM2.5-induced cytotoxicity by regulation of oxidative stress-ER stress-autophagy-apoptosis signaling axis. | [35] | |
| LBP | Zebrafish embryos | SA-β-gal activity assay; Survival rate assay; The relative mRNA expression of p53, p21, Bax, Mdm2 and TERT. | The effects of LBP on cell apoptosis and aging might be mediated by the p53-mediated pathway. | [36] | |
| Ginseng Chuanminshen violaceum polysaccharides (CVPs) | D-Gal-induced-aging mice | In-vitro study: DPPH, hydroxyl, and superoxide anion radicals scavenging activity assay. In-vivo study: Body weight and organ indexes assay; T-SOD, Mn-SOD, Cu/Zn-SOD and CAT activity assay; MDA content; The relative mRNA expression of Cu/Zn-SOD, Mn-SOD, CAT, GPx, thioredoxin 1 (Trx1), and thioredoxin 2 (Trx2). | CVPs show anti-aging effect by increasing antioxidant activity. | [37] | |
| Ginsenoside residue polysaccharides (GRPs) | C. elegans | Lifespan assay; LF and ROS level; SOD activity; Microbiomic and transcriptomic analysis. | GRPs prolong lifespan and alleviate aging of C. elegans without affecting locomotive behaviors by increasing antioxidant activity, altering composition of gut flora and inducing preferential synthesis of beneficial fatty acids. | [38] | |
| Sweet tea Rubus suavissmus polysaccharides (STP-60a) | C. elegans and its mutant strains | Lifespan assay; LF and MDA content; The survival rate under heat stress and oxidative stress assay; Pharyngeal pump rate; The activities of SOD, CAT and GPX; ROS level; The relative mRNA expression of daf-16, skn-1, hsf-1, and their target genes. | STP-60a activates the autophagy system of nematodes through insulin and mitochondrial signaling pathways, enhances the antioxidant capacity, and ultimately promotes the longevity of C. elegans. | [39] | |
| Dangshen Codonopsis pilosula polysaccharides (CPs); Sulfated Codonopsis pilosula polysaccharides (SCPs) | H2O2-treated RAW 264.7 cells; Mice with acute oxidative injury | Cell viability and apoptosis assay; Biochemical index assay; SOD, CAT and GPX activity; MDA and ROS level; The relative mRNA expression of Keap1 and Nrf2. | Anti-aging activities of CP and SCP are mediated by activating Keap1/Nrf2 signaling pathway to enhance activity of antioxidant system. | [40] | |
| Yulangsan Millettia pulchra Kurz polysaccharide (YLSP) | D-Gal-induced-aging mice | General appearance, body weight, and organ index assay; The activities of SOD, CAT, T-AOC and GPX; The level of MDA, IL-2, IL-6 and AGEs; The content of p53 and p21. | YLSP may have a protective effect suppressing the aging process by enhancing antioxidant activity and immunity, as well as modulating aging-related gene expression. | [41] | |
| Akebia trifoliata fruit polysaccharides (ATFPs) | C. elegans | In-vitro study: 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonate) (ABTS) and hydroxyl radical-scavenging assay. In-vivo study: Lifespan; SOD, CAT, GPX activity; MDA and ROS level; LF content; mRNA levels of sir-2.1, daf-16, and daf-12. | ATFPs prolong lifespan of C. elegans through improving activity of antioxidant enzymes, that are regulated by sir-2.1, daf-16, and daf-12 in insulin/IGF signaling pathway. | [42] | |
| Red ginseng by-product polysaccharides (RGBPs) | HaCaT cells; SD rats; Male NC/Nga mice with atopic dermatitis-like symptoms and skin lesions | ABTS radical scavenging activity; Toxicity test; Cell viability; MMP-1, MMP-2 and AP-1 content; Typical Th2 chemokine (MDC/CCL22 and TARC/CCL17) level. | RGBPs alleviate skin aging caused by sUV and atopic dermatitis through increasing antioxidant activity, inhibiting AP-1 transactivation, and reducing MDC/CCL22 and TARC/CCL17 level inducted by TNF-α/IFN-γ. | [43] | |
| Angelica sinensis polysaccharide (ASP); Astragalus membranaceus polysaccharide (AMP) | H2O2-treated human fetal lung fibroblast WI-38 cells | Cell viability assay; SA-β-gal activity assay; Telomerase activity assay; Cell-cycle analysis; The content of p53 and p16INK4. | ASP and AMP exert anti-aging activity through improving telomerase activity and regulating p53-p21 and p16-pRb pathways. | [44] | |
| Algal polysaccharides | Kelp Laminaria japonica polysaccharide (LJP) | C. elegans | In-vitro study: DPPH, ABTS and hydroxyl radical-scavenging assay. In-vivo study: Lifespan assay; MDA, ROS, and LF level; T-SOD activity; The relative mRNA expression of Sod-3, Glp-1, Skn-1, Daf-2, Daf-16 and Age-1; Metabolic profiling. | LJP prolongs lifespan of C. elegans and shows anti-aging activity by resisting oxidative stress and promoting alanine, aspartate, and glutamate metabolism, TCA cycle, butanoate metabolism and FoxO signaling pathway. | [45] |
| Red alga Pyropia haitanensis polysaccharide, porphyrin | AD mice | In-vitro study: DPPH-radical scavenging assay. In-vivo study: Learning and memory assay; Activity of AChE and ChAT. | Porphyrin ameliorates learning and memory impairment of AD mice by increasing cerebral acetylcholine content in cortical and hippocampal tissue. | [46] | |
| Asparagus Gracilaria lemaneiformis polysaccharides (GPs) | C. elegans | Lifespan assay; Reproduction; Pharyngeal pumping; Thermotolerance; Oxidative stress; Polyglutamic acid content; DAF-16 level. | Anti-aging activity of GPs is not dependent upon calorie restriction but on insulin pathway DAF-16. | [47] | |
| Hijiki Sargassum fusiforme polysaccharides (SFPs) | Old male ICR mice | Proteomics study. | SFPs promote longevity of mice, which is intensively related to amino acid metabolism, antioxidation and energy metabolism. | [48] | |
| SFPs | HL-7702 cell line; D-Gal-induced-aging mice; Male chronic aging mice | In-vitro study: DPPH and hydroxyl radical-scavenging assay; Cells viability assay. In-vivo study: Ub-Nrf-2, Nrf-2 and p21 level; The relative mRNA expression of Nrf2, Keap1, Nqo1, Mn-SOD, CuZn-SOD, GCLM, GCLC and GPx1. | SFPs decelerate aging process by enhancing Nrf2-dependent cytoprotection, especially antioxidant defense. | [49] | |
| SFPs | Young, middle-aged and aged male ICR mice | The relative mRNA expression of Nrf2, SOD-2, CAT, NQO1 and HO-1; Small intestine microbiota assay. | SFPs ameliorate declined cytoprotective capacity of small intestine in aging process of mice by upregulating the Nrf2/ARE signaling pathway and partially rejuvenating the overall status of small intestine microbiota. | [50] | |
| Fungal polysaccharides | Bolete Lanmaoa asiatica polysaccharides (FLAPs); Yellow mushroom Hohenbuehelia serotina polysaccharides (FHSPs) | C. elegans | Lifespan assay; ROS, LF and MDA level; SOD and CAT activity; Specific gut bacteria and metabolites assay. | FLAPs and FHSPs prolong lifespan of C. elegans by improving the antioxidant system and enriching specific gut bacteria and metabolites without reproductive toxicity. | [51] |
| Maitake Grifola frondosa β-glucans (GFGs); Monkey head mushroom Hericium erinaceus β-glucans (HEGs) | Yeast cells; D. melanogaster | Lifespan assay; ROS level; The relative mRNA levels of RAS2, HXT7, CTT1, and SOD2; α-Synuclein toxicity and its aggregation. | β-Glucans prolong lifespan through inhibiting the Ras/PKA pathway, reducing the toxicity of α-synuclein, and suppressing its aggregation. | [52] | |
| Grifola frondosa intracellular zinc polysaccharides (IZPs) | D-Gal-induced-aging mice | In-vitro study: Hydroxyl radical, DPPH radical, superoxide radical, hydrogen peroxide-scavenging assay; Antibacterial activity. In-vivo study: T-AOC and SOD activity; MDA content; Histopathology analysis. | IZPs show anti-aging effect by increasing antioxidant and antibacterial activities of mice. | [53] | |
| Golden mushroom Flammulina velutipes sulfated polysaccharides (SFPs) | D-Gal-induced-aging mice | In-vitro study: Hydroxyl radical, DPPH radical, superoxide radical-scavenging effect assay. In-vivo study: Hematological parameters and serum biochemical indexes assay; SOD, GPX, CAT and T-AOC activity; MDA and LPO content; AchE and nitric oxide synthase (NOS) activity; Histopathology analysis. | SFPs show protective abilities against aging by increasing antioxidant activities, improving inflammatory response and ameliorating the anile condition of mice without disturbing general condition and physiology. | [54] | |
| White button mushroom Agaricus bisporus polysaccharides (WMPs) | D-Gal-induced-aging mice | Animal behavioral tests; SOD and GPX activity; MDA content; TNF-α, IL-1β and IL-6 level; Gut microbiota assay; Short-chain fatty acid (SCFA) level. | WMPs improve locomotor activity and the spatial and recognition memory of aging mice by alleviating oxidative stress, decreasing pro-inflammatory cytokine levels, and increasing the SCFA level and abundance of beneficial bacteria. | [55] | |
| Agaricus bisporus acidic-extractable polysaccharides (AcAPs) | D-Gal-induced-aging mice | Serum biochemical indexes assay; SOD, GPX, CAT activity; MDA content; Histopathology analysis. | AcAPs show anti-aging effects by increasing antioxidant activity and alleviating oxidative stress. | [56] | |
| Agaricus bisporus enzyme-assisted polysaccharides (EnAPs) | D-Gal-induced-aging mice | In-vitro study: Reducing power assay; hydroxyl radical and DPPH radical-scavenging effect assay; Fe2+-chelating rates. In-vivo study: SOD, GPX, CAT activity; MDA content; Histopathology analysis. | EnAPs show anti-aging effects by increasing antioxidant activity, improving organ function and remitting lipid metabolism. | [57] | |
| β-1,3-Glucans | Aged N. guentheri | Lifespan assay; LF content; SA-β-Gal activity; ROS, protein oxidation and lipid peroxidation level; CAT, SOD and GPX activity; The level of p66Shc. | β-1,3-Glucans show anti-aging effects by increasing antioxidant activity. | [58] | |
| β-1,3-Glucans | Young, middle-aged and aged mice | DTH response assay; Hematologic index and biochemical parameter assay; The levels of KLH-specific IgG, IgG1 and IgG2a; Cellular composition of splenocytes and proliferation of splenocytes assay. | β-1,3-Glucans exert anti-aging effects by enhancing the adaptive immune responses of aged mice without disturbing their general condition and physiology. | [59] | |
| Tremella fuciformis polysaccharides (TFPs) | H2O2-treated human dermal fibroblasts-neonatal (HDF-n) | Cell viability and apoptosis assay; ROS level; Levels of p16, p21, p53 and SIRT-1. | TFPs attenuate H2O2-induced cell oxidative stress and apoptosis through the upregulation of the SIRT1 pathway. | [60] |
Table 2.
Anti-aging effects and modes of action of polyphenols.
| Subclasses of Polyphenols | Representative Components | Models | Main Indicators of Aging | Modes of Action | Reference |
|---|---|---|---|---|---|
| Phenolic acids | Chlorogenic acid (CGA) extracted from coffee and tea | C. elegans | Lifespan assay; Thermotolerance and stress resistance assay; The relative mRNA expression of FoxO transcription factors daf-16, hsf-1, skn-1 and hif-1. | CGA extends lifespan of C. elegans via DAF-16 in insulin/IGF-1 signaling pathway. | [74] |
| p-Coumaric acid | C. elegans | Lifespan assay; Stress resistance assay; ROS level; The relative mRNA expression of daf-16, skn-1, sod-3, osr-1, osm-7, osm-11 and ama-1. | p-Coumaric acid increases oxidative resistance of C. elegans by regulating skn-1, an ortholog of Nrf2. | [75] | |
| Caffeic acid (CA); Dihydrocaffeic acid (DHCA) | C. elegans | Lifespan and stress assay; The relative mRNA expression of the genes daf-16, daf-18, skn-1, ctl-1, hsp-16.2, hsf-1, sod-3, and sir-2.1. | CA and DHCA promote longevity and increase stress resistance in C. elegans by activating the DAF-16/FoxO transcription factor and modulating the expression of stress-related genes. | [76] | |
| Flavonoids | Quercetin | C. elegans | Lifespan assay; Evaluation of motility; Stress resistance assay; ROS level; The relative mRNA expression of daf-2, age-1, daf-16, nsy-1, sek-1, pmk-1, skn-1 and hsf-1. | Quercetin induces heat-stress tolerance in C. elegans by modulating HSF-1 expression and/or activity. | [77] |
| Quercetin | H2O2-induced senescence vascular smooth muscle cell (VSMC) | Cell viability assay; SA-β-gal activity; Apoptosis assay; The content of Bax and Bcl-2. | Quercetin alleviates H2O2-induced VSMC senescence by regulating apoptosis through the P53-P21 and P16 pathways. | [78] | |
| Quercetin; Rutin | AD model mice | GSH/GSSG ratio; MDA content; CAT, SOD and GPX activity; BACE1 activity; The relative mRNA expression of cat, sod, gpx, APP, BACE1, ADAM10, caspase-3, caspase-6, IL-1β, TNF-α and IFN-γ. | Quercetin and rutin both alleviate the aging phenotype of AD mice by augmenting intracellular redox homeostasis in the brain. | [79] | |
| Anthocyanins from purple wheat | C. elegans and its mutant strains | In-vitro study: DPPH free radical scavenging assay. In-vivo study: Lifespan assay; The relative mRNA expression of hsp-16.2; ROS level; DAF-16 location. | Anthocyanins extend the lifespan of C. elegans mainly by regulating the DAF-16/FoxO signaling pathway. | [80] | |
| Anthocyanins from honeysuckle Lonicera pallasii | D. melanogaster | Lifespan assay; Stress resistance, locomotor activity and intestinal integrity assay; The relative mRNA expression of eEF1α2, RpL32, Hsp27, Hsp68, Hsp83, Keap1, NRF, Sod1, HIF1, Clk and Per; Radical scavenging and antioxidant activity assay. | Honeysuckle anthocyanins prolong lifespan and improve the health span of D. melanogaster through enhancing antioxidant activities. | [81] | |
| Tart cherry extract (TCE) | C. elegans and its mutant strains | Lifespan assay; The relative mRNA expression of daf-16, daf-2, daf-18, aak-2, akt-1, lin-14, skn-1, ucp-4, sod-2/3; Mitochondrial respiration analysis. | TCE confers health span benefits to C. elegans through enhanced mitochondrial function and reduced oxidative stress, mainly via the DAF-16 pathway. | [82] | |
| Stilbenes | Resveratrol | D. melanogaster | Longevity and fecundity assay; Locomotor activity; SOD and CAT activity assay. | Resveratrol prolongs the lifespan of both male and female adult fruit flies by scavenging ROS and neuroprotection through increasing antioxidant enzyme activity. | [83] |
| Resveratrol | Aged N. guentheri | Lifespan assay; Cognitive ability and locomotor activity assay; Neurofibrillary degeneration assay; SA-β-gal activity; LF content. | Resveratrol prolongs the lifespan of aged fish by retarding neurodegeneration and aging-related histological markers. | [84] | |
| Resveratrol | Aged N. guentheri | SA-β-gal activity; LF content; Histological evaluation of ovarian development; PCNA, SIRT1 and GRP78 content; The relative mRNA expression of NRF2, NF-κB, IL-1β, TNF-α, IL-8, GRP78 and CHOP. | Resveratrol activates SIRT1/NRF2 to reduce inflammation and ER stress so as to delay ovarian aging in N. guentheri. | [85] | |
| Resveratrol | HtrA2 knockout mice | Motor phenotype assay; Survival assay; The relative mRNA expression of chop, atf4, p53, noxa, bcl2, bax, dr5; NeuN staining assay. | Resveratrol alleviates neural aging by attenuating apoptosis at the level of Bax. | [86] | |
| Resveratrol | 18-month-old SD rats anaesthetized by sevoflurane and nitrous oxide | Learning and memory assay; The content of SIRT1, Poly ADP-ribose polymerases-1 (PARP-1), cleaved caspase-3 and Bax. | Resveratrol improves learning and memory ability and inhibits neuronal apoptosis by increasing the expression of SIRT1 in aged rats after general anesthesia. | [87] | |
| Resveratrol | 6-, 9-, 12-month-old N. guentheri | SA-β-gal activity assay; The relative mRNA level of IL-8, IL-10, SIRT1, NF-κB; The content of TNFα, SIRT1, RelA/p65, p-IκBα, IκBα and LGR5. | Resveratrol delays the aging of the annual fish N. guentheri by inhibiting SASP through the SIRT1/NF-κB signaling pathway. | [88] | |
| Resveratrol | Young, middle-aged and aged rats | DTH response assay; Hematologic index and biochemical parameter assay; The levels of KLH-specific IgG, IgG1 and IgG2a; Cellular composition of splenocytes and proliferation of splenocytes assay. | Resveratrol exerts an anti-aging effect by enhancing the adaptive immune responses of aged rats without disturbing their general condition and physiology. | [89] | |
| Resveratrol | Senescence-accelerated mice (SAM) | The relative mRNA expression of TNF-α, IL-1β, IL-10, Bcl-2-associated death promoter (BAD), Bcl-2-associated X protein (BAX), B-cell lymphoma 2 (Bcl-2), X-linked inhibitor of apoptosis protein (XIAP), SIRT1, FoxO1 and FoxO3A; The content of TNF-α, IL-1β, IL-10, NF-κB p65, NF-κB p50–105, NF-κB p52–100, inhibitor of NF-κB (IκB)-β and -α, BAD, BAX, and Bcl-2; The activity of GPX, glutathione reductase (GR), and glutathione transferase (GST); Plasma glucose and insulin assay. | Resveratrol improves the pancreas aging of SAM by modulating the inflammatory, oxidative and apoptotic status related to aging. | [90] | |
| Lignans | Sesamin from sesame seed | β-Amyloid-induced-aging C. elegans model | Aβ-induced paralysis assay; The relative mRNA expression of Aβ transgene; β-Amyloid content; Chemotaxis behavior assay; Lifespan assay. | Sesamin prolongs the lifespan of an β-amyloid-induced-aging C. elegans model by reducing Aβ toxicity. | [91] |
| Sesamin | C. elegans Bristol strain N2 and its mutant strains | Lifespan assay; Bacterial infection assay; Locomotory scoring assay; Stress resistance assay; LF content; Protein oxidant assay; Brood size assay. | Sesamin enhances the host defense of C. elegans and increases average lifespan via the activation of both skn-1 (encoding a component of the p38 MAPK pathway) and daf-16 (encoding a component of the IGF-1 pathway). | [92] | |
| Tannins | Tannic acid (TA) | C. elegans strain N2 and its mutant strains | Lifespan assay; Stress resistance; Nematode length and reproduction assay; Pharynx pumping rate. | TA influences the aging process by regulating sek-1. | [93] |
| ellagic acid (EA) | C. elegans strain N2 and its mutant strains | Lifespan assay; Stress resistance; Antimicrobial capacity assay; Length and reproduction assay; Pharynx pumping rate; Triglyceride assay. | EA influences the aging process by regulating antimicrobial effects and hormetic action. | [94] | |
| Oenothein B (OEB) | Wild-type C. elegans strain and its mutant strains | Lifespan assay; Reproduction assay; Pharynx pumping rate; Locomotion and thermotolerance assay; ROS level; SOD content; Age pigment content. | OEB might modulate multiple genetic pathways involved in insulin/IGF-1 signaling (IIS) via age-1 and daf-16, the dietary restriction (DR) pathway via eat-2 and sir-2.1, and the mitochondrial electron transport chain via isp-1 to promote healthy lifespan. | [95] | |
| Pentagalloyl glucose (PGG) | Wild-type C. elegans strain and its mutant strains | Lifespan assay; Reproduction assay; Pharynx pumping rate; Locomotion and thermotolerance assay; ROS level; SOD content; Age pigment content. | PGG and its metabolites promote healthy lifespan by regulating the IIS and DR pathway and the mitochondrial electron transport chain. | [96] |
Table 3.
Anti-aging effects and modes of action of carotenoids.
| Subclasses of Carotenoids | Representative Components | Models | Main Indicators of Aging | Modes of Action | Reference |
|---|---|---|---|---|---|
| Carotenes | β-Carotene | Aged MSCs induced by H2O2; Aged mice | In-vitro study: Content of p16 and p21; DNA damage and cell proliferation assay; Levels of IL-1 β, IL-6 and TNF-α; Levels of ROS and MDA; SOD activity; Level of KAT7 and P15. In-vivo study: Psychology and physiology behaviors of aged mice; Inflammation and tissue fibrosis levels. | β-Carotene inhibits aging by regulating the KAT7-P15 signaling axis. | [112] |
| Lycopene | 10-month-old adult mice | Hematology and clinical biochemistry indexes assay; MDA content; CAT, SOD and GPX activity. | Lycopene alleviates aging by increasing antioxidant enzyme activity. | [113] | |
| Lycopene | D-Gal-induced and naturally aging hens (Gallus domesticus) | Morphological and ultrastructure assay; Somatic cell proliferation assay; Levels of Bax, Bcl-xL, PCNA, CDK2 and CCND1; GSH, ROS and MDA contents; T-SOD, CAT, GPX and T-AOC activity; Levels of Nrf2, p-Nrf2, HO-1 and NQO1. | Lycopene ameliorates the aging of hen ovaries by inhibiting oxidant stress and apoptosis via the activation of the Nrf2/HO-1 pathway. | [114] | |
| trans-Lycopene from tomato juice | 28 patients (mean age 69.7 ± 3.1 years; mean BMI 31.5 ± 3.6 kg/m2) at high cardiovascular risk | Plasmatic carotenoids, ICAM-1, VCAM-1, and C-reactive protein (CRP) levels assay. | Trans-lycopene may attenuate the risk of cardiovascular disease by reducing the concentration of important inflammatory molecules related to atherosclerosis. | [115] | |
| Lycopene | Aβ1–42-induced AD rats | Behavioral parameters assay; Serum levels of TNF-α, IL-1β and IL-6β; The mRNA expressions of TLR4, p65; The content of TLR4, NF-κB-p65, β-APP, PS-1 | Lycopene significantly improves cognitive deficits by blocking the activation of NF-κB p65 and TLR4 expressions and the production of cytokines, thereby endorsing its usefulness for diminishing β-amyloid deposition in the hippocampus tissues. | [116] | |
| Crocin | Middle-aged (15 months old) rats | Serum parameters assay; SOD, CAT, GPX, GR, GST, Na+/K+ ATPase, Ca2+ ATPase, AChE, CS and CCOX activity; GSH, LPO, PCC, ROS, NO, LF and acetylcholine levels; Histopathology assay. | Oral supplementation of crocin reverses the aging of rats through the suppression of oxidative stress and neuroinflammatory responses. | [117] | |
| Xanthophylls | Astaxanthin (ATX) | D-Gal-induced-aging rats | Activities of SOD, CAT and GPX; MDA content; Serum levels of IL-2, IL-1β, IL-6, IgM and IgG; Nrf2, Keap1, NF-κB (p65) and IκBα level. | The anti-aging effect of astaxanthin is in part due to Nrf2/Keap1 and NF-κB pathways, which regulate oxidative stress and immune impairment, respectively. | [118] |
| ATX | Young and aged male mice | Level of MDA, NO, APOPs and GSH; CAT and SOD activity; | ATX alleviates brain aging by suppressing oxidative stress. | [119] | |
| ATX | Wild-type yeast Saccharomyces cerevisiae and antioxidant-deficient strains | Survivability assay; Antioxidant biomarkers assay; Apoptotic markers assay. | ATX enhances the longevity of yeast S. cerevisiae by reducing oxidative stress and apoptosis. | [120] | |
| ATX | Glutamate-treated mouse hippocampal HT22 cells | Cell viability assay; LDH activity assay; ROS content; Caspase activity and PARP cleavage assay; The relative mRNA expression of HO-1; The content of HO-1, Nrf2, p-Akt, Akt, GSK3b, p-GSK-3b (Ser9), Bcl-2, Bax, AIF, cytochrome-c (Cyto-c), PARP. | ATX alleviates glutamate excitotoxicity-related neuronal loss associated with Alzheimer’s disease by regulating oxidative stress and apoptosis through the Akt/glycogen synthase kinase-3b (GSK-3b) signaling pathway. | [121] | |
| Krill oil (rich in ATX) | Aged N. guentheri | Lifespan assay; Histological assay; LF content; SA-β-Gal activity; ROS, protein oxidation, lipid peroxidation and p66Shc level; CAT, SOD and GPX activity; The relative mRNA expression of interferon-γ, tnf-α and il10; The content of IκBα, p-IκBα, p65 and p-p65. | KO exerts its anti-aging and rejuvenation effects via the enhancement of the antioxidant system and suppression of the NF-κB signaling pathway. | [122] | |
| Canthaxanthin | Aging model liver cell (AML12) exposed to H2O2; Liver fibrosis mice model induced by CCL4 | In-vitro study: SA-β-Gal activity; P16, P21, γ-H2A, 53BP1, HP1α and H3K9me3 levels; The relative mRNA expression of IL-6, IL-1β, TNF-α, CXCL1 and MMP-1; Level of SIRT6, NF-κB, p-NF-κB, JAK2, p-JAK2, STAT1 and p-STAT1; Levels of ROS, MDA, SOD and GSH. In-vivo study: Histological analysis; Serum levels of ALT and AST; Levels of TNF-α, IL6, IL-1β, COL1a1 and α-SMA; Phosphorylation level of Smad2/3 protein. | Canthaxanthin alleviates liver aging and fibrosis by suppressing inflammation and oxidative stress, which it achieves by regulating SIRT6. | [123] | |
| Lutein | Fibroblasts exposed to UVA or UVB | Cell viability assay; Membrane integrity; MMP-1, MMP-2, TIMP-1, TIMP-2 and elastin protein levels; MMP-1 promoter activity. | Lutein alleviates fibroblast aging induced by UVA or UVB radiation through the inhibition of the MMP to TIMP ratio, cell loss, membrane damage and elastin expression. | [124] | |
| Lutein | Human RPE cell line ARPE-19 treated with H2O2 | Cell viability assay; Lysosome and ROS content; SA-β-Gal activity; Cell cycle; The content of p-SIRT1, SIRT1, SIRT3, p-p53, p53, p21, HO-1, NQO1 and Nrf2. | Lutein protects cells from cellular senescence induced by oxidative stress by upregulating antioxidant effectors. | [125] |
Table 4.
Anti-aging effects and modes of action of sterols.
| Subclasses of Sterols | Representative Components | Models | Main Indicators of Aging | Modes of Action | Reference |
|---|---|---|---|---|---|
| Phytosterols | Diosgenin (DG) | Aged N. guentheri | Lifespan; LF content; SA-β-Gal activity; ROS, protein oxidation and lipid peroxidation level; CAT, SOD and GPX activity; 20S proteasome activity; PI3K/AKT/mTOR activity; The relative mRNA expression of pten, tsc1 and tsc2. | DG exerts its rejuvenation and anti-aging activity by inhibiting the PI3K/AKT/mTOR signal pathway and promoting the ubiquitin–proteasome pathway and antioxidant enzyme activity; they all play prominent roles in ROS production. | [138] |
| β-Sitosterol | H2O2-treated HDF and HaCaT cells | Cytotoxicity of β-sitosterol; Hyaluronic acid (HA) content; Levels of hyaluronic acid synthases (HAS1, -2, -3) and hyaluronidases (HYAL1, -2, -3); Levels of aquaporin3 (AQP3), loricrin (LOR), filaggrin (FLG) and involucrin (IVL). | β-Sitosterol prevents skin aging by promoting the biosynthesis of HA and enhancing skin barrier function. | [139] | |
| Daucosterol palmitate (DSP) extracted from Alpinia oxyphylla Miq | Male AD rat model | Spatial learning and memory test; ROS level; Histological examination; Synaptophysin level. | DSP ameliorates Aβ-induced learning and memory impairment in rats by inhibiting ROS production, preventing hippocampal CA1 neuronal damage and restoring hippocampal synaptophysin. | [140] | |
| β-Sitosterol | Dexamethasone-induced muscle atrophy mice model and C2C12 myoblasts | Mice grip strength and treadmill analysis; Weight of muscles; Muscle fibers; Muscle tissue histological analysis; MAFbx, MuRF1, FoxO1 and FoxO3 level. | β-Sitosterol alleviates aging sarcopenia by downregulating transcriptional factor FoxO1, making FoxO1 unable to affect the expression of muscle atrophy F-box (MAFbx), ultimately inhibiting muscle atrophy. | [141] | |
| β-Sitosterol | TNF-α-treated GT1-7 cells (a cell line of GnRH neurons) | Membrane sterols test; Gonadotropin-releasing hormone (GnRH) release assay; Levels of NF-κB and p-IκBa. | β-Sitosterol prevents TNF-α-induced GnRH decline through the inhibition of NF-κB activation via the ER-mediated inhibition of IκB processing. | [142] | |
| Animal sterols | Vitamin D3 | D-Gal-induced-aging male rats | MDA content; SOD, GSH and CAT activity; GCNA and PCNA content; Anti-apoptotic (BCL2) and apoptotic (BAX and active caspase-3) assay; TUNEL immunohistochemical assay; Heat shock protein1 a1 (HSP1A1), AGE-receptor (AGER), vitamin D and advanced glycation end products (AGE) level. | Vitamin D3 improves age-associated spermatogenesis impairment by regulating apoptosis and the antioxidant system, which are involved in the AGER and HSP1A1 pathway. | [143] |
| Vitamin D | Human lung carcinoma A549 cells, human B-cell lymphoblastoid TK6 cells, and human peripheral blood lymphocytes treated with H2O2 | Detection of histone H2AX phosphorylation and ATM activation; ROS level; Analysis of cellular fluorescence. | Vitamin D exerts an anti-aging effect by attenuating DNA damage. | [144] | |
| Mussel (Mytilidae) sterols | Wild-type and mutant-type Saccharomyces cerevisiae | Lifespan assay; ROS level; MDA content; The relative mRNA expression of uth1, skn7, tub1. | The anti-aging effect of mussel sterols depends on their antioxidative ability and regulation of uth1, skn7, tub1 expression. | [145] | |
| Fungal sterols | Ergosterols from Ganoderma lucidum spores | Wild-type and mutant-type Saccharomyces cerevisiae | Replicative lifespan; The relative mRNA expression of sod1 and sod2. | Ganoderma lucidum ergosterols prolong the replicative lifespan of yeast by regulating uth1 expression. | [146] |
| Chinese cordyceps cerevisterol | H9C2 cells; ICR mice | In-vitro study: Cell survival rate assay; Level of MAPK1, MAPK3, VEGFA, AKT1, PIK3CA and RAC1. In-vivo study: Angiogenic test. | Chinese cordyceps cerevisterol exhibits anti-aging and anti-fatigue effects by improving the body’s hypoxia tolerance through the VEGF signal pathway. | [147] |
Table 5.
Anti-aging effects and modes of action of terpenoids.
| Subclasses of Terpenoids | Representative Components | Models | Main indicators of Aging | Modes of Action | Reference |
|---|---|---|---|---|---|
| Hemiterpene | Prenol | Wild-type and mutant-type C. elegans | Toxicity assessment; Lifespan assay; Amyloid-β-mediated paralysis, stress resistance and chemotaxis assays; Level of α-synuclein and ROS; The relative mRNA expression of sod-1, sod-2, sod-3, gst-3, gst-4, hsp 16.2, hsp-70, daf-16, skn-1 and hsf-1. | Prenol improves the lifespan and health span of worms by regulating transcription factors DAF-16, HSF-1 and SKN-1. | [170] |
| Monoterpenoids | Cuminaldehyde extracted from cumin | SH-SY5Y cells; C57BL/6J male mice | In-vitro study: Cell survival assay. In-vivo study: Spatial learning and memory assay; The relative mRNA expression of Bdnf, Icam, ApoE, TNF-α and IL-6. | Cuminaldehyde exerts neuroprotective effects through the modulation of genes coding for neurotrophic factors and inflammatory factors. | [171] |
| Asperuloside extracted from Du Zhong Eucommia ulmoides male flower | C. elegans | Motor competency assay; Mitochondrial respiratory capacity; ATP content; ROS level; DAF-16 level; Metabolomics detection; RNAi interference assay for daf-16. | Asperuloside delays the muscle aging of C. elegans through a daf-16-mediated improvement in mitochondrial dysfunction. | [172] | |
| Limonene | HaCaT cells treated with UVB | Cell viability assay; ROS level; HO-1, NQO-1 and γ-GCLC content; Nrf2 knockdown assay; Levels of α-MSH, p53, claudin, occuludin, ZO-1 and MMP-2. | Limonene displays a dermato-protective effect in skin cells by activating the Nrf2-dependent cellular antioxidant defense system. | [173] | |
| Carvacrol (CAR) | D-Gal-induced-aging rats | TAC and GPX activity; GST level; MDA content; The relative mRNA expression of p53, p21 and Bax. | CAR attenuates aging by suppressing oxidative stress. | [174] | |
| Sesquiterpenoids | Dihydro-β-agarofuran-type sesquiterpenoid | C. elegans | Lifespan assay; The relative mRNA expression of skn-1, hsf-1 and daf-16. | Dihydro-β-agarofuran-type sesquiterpenoids prolong the lifespan of worms by regulating transcription factors skn-1 and hsf-1. | [175] |
| α- and β-Santalol | Wild-type and mutant-type C. elegans | Lifespan assay; ROS level; Stress resistance assay; Toxic amyloid-β and polyglutamine repeat (Q35, Q40, and HtnQ150) aggregation assay; Neuronal survival assay; LF accumulation; RNAi interference assay for skn-1 and let-23; The relative mRNA expression of gst-4, gcs-1, gst-10, gsr-1, hsp-4 and skr-5. | Both α- and β-Santalol alleviate aging by selectively regulating SKN-1/Nrf2 and EOR-1/PLZF transcription factors through the RTK/Ras/MAPK-dependent signaling axis. | [176] | |
| Patchouli alcohol (PA) extracted from patchouli Pogostemon cablin | D-Gal-induced-aging mice; Chondrocytes isolated from D-Gal induced-aging mice | In-vitro study: Cell survival assay; The relative mRNA expression of col2a1, mmp13, Tp53, CDKN1A, cat, gss, sod, Nrf2, HO-1, Keap1 and NQO1; Content of Acan, Col2a1, Adamts5, Mmp13, TP53 and P21. In-vivo study: Mental state, body weight and organ index assay; Histopathological assay; Cartilage quality assay; The relative mRNA expression of Tp53, Cdkn1a/p21Cip1/Waf1, Cdkn2a/p16INK4a, Nrf2, HO-1, cat and sod; CAT and SOD activity; GSH and MDA level. | PA inhibits D-Gal-induced chondrocyte senescence via the activation of the antioxidative system, which is attributable to the activation of the Nrf2/HO-1 pathway. | [177] | |
| Diterpenoids | Mushroom Hericium erinaceus mycelium (HEM) and its diterpenoid derivative, erinacine A (EA) | 15-month-old mice | Spatial learning ability assay; The mRNA expression of TNFα, IL-1β, NGF and NeuN; Body weight and fat pad weight assay; Serum chemistry analysis. | HEM and EA minimize the progression of aging and obesity-induced neurodegeneration by reducing metabolic abnormalities and neuroinflammatory cytokines and increasing neurogenesis factors. | [178] |
| Carnosol extracted from Rosmarinus | Wild-type and mutant-type C. elegans | Lifespan assay; ROS level; CAT, SOD and GPX activity; MDA content; Stress resistance, mobility, fertility and paralysis assay; Age pigment and body fat accumulation; The relative mRNA expression of sod-3, sod-5, hsf-1, hsp-16.1, hsp-16.2, daf-16 and hsf-1; Subcellular localization of DAF-16. | Carnosol-mediated longevity requires the upregulated expression of sod-3, sod-5, hsf-1, hsp-16.1 and hsp-16.2 and is dependent on hsf-1 gene. | [179] | |
| Andrographolide (ANDRO) extracted from Chuan Xin Lian Andrographis paniculata | Adult and aged Octodon degus | Recognition memory, preference for novel experiences, social recognition and long-term memory assay; Level of glutamate ionotropic receptor AMPA type subunit 1 (GLUR-1), glycogen synthase kinase-3β (GSK-3β), phosphorylated glycogen synthase kinase-3β (p-GSK-3β), Homer, N-methyl D-aspartate receptor subtype 2B (NR2B), post-synaptic density 95 (PSD95), synaptotagmin I/II (SYT), synaptophysin (SYP) and gamma-aminobutyric acid receptor (GABAA). | ANDRO administration shows improved complex behaviors related to age-detrimental effects by modulating mechanisms of synaptic transmission and proteins. | [180] | |
| Triterpenes | Compound K (CK) extracted from herb Panax ginseng | Hydrobromide-induced memory impairment mice | Production and clearance of Aβ; SOD, MDA, and GSH levels; Bcl-2, Bax and Caspase-3 levels; The relative mRNA expression of Nrf2 signaling pathway-related factors Nrf2, Keap1 and HO-1. | CK improves impaired memory function by inhibiting apoptosis and enhancing stress resistance through the Nrf2/Keap1 signaling pathway. | [181] |
| CK | Vascular-dementia (VD) rats | Cognitive ability assay; Histopathological alterations assay; The deposition of Aβ1–42; The contents of Ser473-Akt/Akt, pSer9-GSK3β/GSK3β and insulin degrading enzyme (IDE). | CK might attenuate cognitive deficits and Aβ1–42 deposition in the hippocampus by enhancing the expression of pSer9-GSK-3β and IDE. | [182] | |
| CK | Mouse embryonic fibroblast NIH3T3 cells treated with UVB | Cell viability assay; The mRNA expression levels of MMP1, COX-2, filaggrin (FLG), transglutaminase (TGM), hyaluronic acid synthases (HAS)-1, 2, and 3, type I collagen; Type I collagen promoter activity assay; Melanin formation and secretion assay; Tyrosinase activity assay; The content of κBα/p-κBα, and JNK/p-JNK, ERK/p-ERK, and p38/p-p38. | CK has ability to increase skin moisture levels and melanin synthesis as well as protect against UVB-induced photo-aging by regulating the p38/AP-1/CREB pathway. | [183] | |
| Ginsenoside Rg1 (Rg1) | Sca-1+ HSC/HPC cells harvested from D-Gal-induced-aging rats | SA-β-Gal activity; Cell-cycle assay; CFU-mix assay; The mRNA expression of cleaved caspase 3, Bcl-2, Bax, SIRT3 and SOD2; The content of SIRT3 and SOD2. | Rg1 conducts functions of anti-aging in Sca-1+ HSC/HPC cells in D-gal-induced-aging rats by inhibiting mitochondrial pathway-mediated apoptosis and activating the SIRT3/SOD2 signaling pathway. | [184] | |
| Ginsenoside Rb1 (GRb1) | Young and natural aging C57BL/6J mice | Morphological and histological analysis; The relative mRNA expression of PAI-1, Mmp12, Tert, p53, p21, Cdk2, Bax, Caspase-3, IL-1β, IL-6, IL-8 and TNF-α; The content of p53, p21, Cdk2, Bax, Cleaved caspase-3, NF-κB, p-NF-κB; Metabolomics analysis. | GRb1 retards the aging process in natural-aging C57BL/6J mice by regulating the cell cycle and apoptotic pathway, which are associated with the alleviation of metabolic disorders. | [185] | |
| 20-O-β-D-glucopyranosyl20(S)-protopanaxadiol (20GPPD), the primary bioactive metabolite of ginsenoside Rb1 | Human keratinocytes HaCaT | Cell viability assay; The content of HA and hyaluronan synthase 2 (HAS2); The level of ERK, Akt, p-ERK, p-Akt, Src and p-Src. | 20GPPD enhances the production of HA by acting as an upstream modulator of ERK and Akt activity mediated by Src kinase in human keratinocytes. | [186] | |
| Ganoderic acid D (GA-D) extracted from Ganoderma lucidum | Human amniotic mesenchymal stem cell (hAMSC) treated with H2O2 | SA-β-Gal activity; Telomerase activity assay; Cell viability assay; ROS level; Osteogenic and chondrogenic differentiation of hAMSCs assay; Cell-cycle assay; The relative mRNA expression of 14-3-3ζ, PRDX3, SIRT1-7, β-Catenin, ERK1, ERK2; The content of p21, p16, Nrf2, PERK, p-PERK, and peroxidase III (PRDX3). | GA-D retards hAMSC senescence through the activation of the PERK/NRF2 signaling pathway. | [187] | |
| GA-D | hAMSCs treated with or without GA-D; Mice treated with or without GA-D | In-vitro study: 14-3-3ε-Encoding gene (YWHAE) knockdown assay; SA-β-Gal activity assay; Cell viability assay; ROS level; Differentiation of hAMSCs assay; Cell-cycle assay; The content of p21, p16, 14-3-3ζ, t-Nrf2, n-Nrf2, HO-1, NQO1, CaM, p-CaMKII, CaMKII, p16INK4a; The relative mRNA expression levels of 14-3-3ε, n-Nrf2, t-Nrf2, CaM, CaMKII, p-CaMKII, HO-1, NQO1, p16INK4a, and p21; In-vivo study: Histopathological assay; Activity of T-AOC, SOD, GPX, and content of MDA, AGEs, RAGE assay in the sera. | GA-D retards hAMSC senescence by targeting 14-3-3ε to activate the CaM/CaMKII/Nrf2 signaling pathway. | [188] | |
| Maslinic acid (MA) obtained from Olea europae | Rats pretreated with CCl4 | Plasma lipoperoxide levels and liver lipid peroxidation assay. | MA may offer some advantages in the anti-aging process by decreasing plasma lipoperoxide levels and inhibiting liver lipid peroxidation. | [189] | |
| Ursolic acid (UA) | Skeletal muscle satellite cells, isolated from 10-days old mice, treated with or without UA; 10 months aged mice treated with UA | In-vitro study: Cell viability assay; The relative mRNA levels of paired-box 7 (PAX7), Myogenin, peroxisome proliferator-activated receptor gamma (PGC-1α) and SIRT1; Immunostaining assay. In-vivo study: The content of myoglobin; The concentration of ATP and ADP; Histopathological assay; Satellite cell proliferation assay. | UA promotes skeletal muscle rejuvenation by enhancing SIRT1 expression and satellite cell proliferation. | [190] | |
| Ursolic Acid (UA), a compound which is extensively present in apple peels | Aged-mice C5BL/6 (20 months old) | The content of SIRT1, SIRT6, PGC-1β and α-Klotho. | UA treatment reverses the aging of the liver by enhancing SIRT1 and SIRT6 levels and promoting the production of PGC-1β and Klotho. | [191] | |
| Cycloastragenol (CA) | C. elegans | Lifespan assay. | CA and its new derivatives could significantly extend the lifespan of C. elegans by regulating SKN-1. | [192] | |
| CA | Human T cells | Cellular proliferative capacity; Telomerase activity; Surface markers and cytokine secretion of human CD4+ and CD8+ T cells. | CA extends T cell proliferation by increasing telomerase activity. | [193] | |
| Platycodin D extracted from Platycodon grandiflorum | C2C12 cells treated with H2O2 | Cell cytotoxicity assay; ROS level; The relative mRNA levels of Bcl-2, Bax and caspase-3; Level of Keap1, Nrf2 and HO-1. | Platycodin D protects C2C12 cells against H2O2-induced oxidative stress and apoptosis through the Keap1/Nrf2/HO-1 signal pathway. | [194] | |
| Ginsenoside Re (GRe) | 4-month-old young male mice and 14-month-old aged male mice, including Klotho wild-type, Klotho-deficient (±) mice, wild-type, GPx-1 KO, non-transgenic (non-TG), and GPx-1 TG mice | Cognitive and memory ability assay; DNA-binding activity assay; The content of JAK2, p-JAK2, STAT3, p-STAT3, angiotensin II AT1 receptor, ET1, GPx-1, ERK, p-ERK, cAMP response element-binding protein (CREB), and p-CREB; NOX activity assay; ROS, lipid peroxidation and protein carbonyl level assay; The relative mRNA level of glutamate-cysteine ligase catalytic subunit (GCLc) and glutamate-cysteine ligase modifier subunit (GCLm); The level of GSH and GSSG; SOD, GPX and GR activity assay. | GRe attenuates all alterations, such as AT1 receptor expression, NOX, ROS, and GPX levels, and cognitive dysfunction in aged Klotho-deficient (±) mice via the upregulation of Nrf2/GPx1/ERK/CREB signaling. | [195] | |
| Ginsenoside Rg1 (Rg1) | Sca-1+ HSC/HPC cells isolated from D-Gal-induced-aging rats | SA-β-gal activity; Cell-cycle analysis; CFU-mix assay; The relative mRNA expression of cleaved caspase 3, B-cell lymphoma-2 (Bcl-2), Bcl-2 associated X protein (Bax), SIRT3, SOD2; The content of SIRT3 and SOD2. | Rg1 conducts functions of anti-aging in Sca-1+ HSC/HPC cells in the D-gal-induced-aging model by inhibiting mitochondrial pathway-mediated apoptosis and activating the SIRT3/SOD2 signaling pathway. | [184] | |
| Rg1 | SAMP8 mice | ROS level; The relative mRNA expression of NOX4, p22phox and p47phox; Pathological examination; Level of collagen IV, TGF-β and NLRP3. | Rg1 reduces age-related liver fibrosis by reducing NOX4-mediated ROS-induced oxidative stress and inhibiting the activation of the NLRP3 inflammasome. | [196] | |
| Rg1 | AlCl3-induced-aging mice | Spatial learning and memory assay; Level of BDNF, TrkB, FGF2, Akt, Bcl-2 and Caspase3. | Rg1 ameliorates cognitive deficits in aging mice by regulating FGF2-Akt and BDNF-TrkB signaling pathways. | [197] |
Table 6.
Anti-aging effects and modes of action of vitamins.
| Subclasses of Vitamins | Representative Components | Models | Main Indicators of Aging | Modes of Action | Reference |
|---|---|---|---|---|---|
| Water-soluble vitamins | Riboflavin (RF) | D. melanogaster treated with H2O2 | Lifespan assay; Reproductive capacity assay; LF content; Activities of SOD and CAT. | RF prolongs the lifespan and increases the reproduction of fruit flies through the antioxidative stress pathway. | [206] |
| Topical liquid formula of polydeoxyribonucleotide (PDRN), vitamin C and niacinamide (a kind of vitamin B3 derivant) | Human primary epidermal keratinocyte, human primary epidermal melanocyte, human fibroblast treated with UV-B; HRM-2 mice treated with UV-B | Melanin content; Contents of NF-κB, Nrf, p-Nrf, HO-1, P53, MITF, Col1a1, Fibrillin1, Fibrillin2, Fibrillin5; mRNA expression of p53, mitf, Mmp2, Mmp3, Mmp9; Activity of NADPH oxidase and SOD. | A topical liquid formula delays skin-aging induced by UV-B by regulating Nrf2 signaling. | [207] | |
| Combination of vitamin C, rice and lupin bio-peptides, hyaluronic acid, and Vichy volcanic mineralizing water | Human keratinocytes and fibroblasts treated with UV-A and pollution | Anti-general oxidant, anti-lipid peroxidation and anti-protein glycosylation ability assays; Activity of collagenase, elastase and hyaluronidase. | A combination of vitamin C, rice and lupin bio-peptides, hyaluronic acid, and Vichy volcanic mineralizing water shows high global antioxidant capacity as well as a protective effect against oxidative stress induced by UV-A, pollution, or both combined factors by stimulating collagen synthesis. | [208] | |
| Vitamin C | Zebrafish treated with LiCl | Expressions of GSK-3β, TSC2, mTOR, FAS, ACC, and ACL; Content of TC, TG and NEFA. | Vitamin C delays liver aging by reducing lipid deposition by regulating GSK-3β/mTOR signaling. | [209] | |
| Fat-soluble vitamins | Vitamin E | DNA repair-deficient mutant mouse (Xpg−/−) | Body weight and tremors assay; SS/SH redox ratio assay; Protein oxidation assay; Histological assay; p53-positive cells assay. | Vitamin E supplementation exerts obvious neuroprotective effect by reducing the number of p53-positive cells. | [210] |
| Vitamin E; Velvet antler polypeptide | D-gal-induced-aging mice | Learning and cognitive abilities assay; Activities of SOD, GPX, and CAT; MDA, PPARα, ACOX1, CPT1A and APOE4 contents; Intestinal microecological analysis. | Vitamin E, or velvet antler polypeptide, exerts anti-aging activity by modulating the gut microbiota and regulating the PPARα/APOE4 pathway. | [211] | |
| Vitamin E and quercetin | Aged breeder hens | Intestinal morphology assay; Serum D-lactate and diamine oxidase content assay; Secretory immunoglobulin A level assay; Expression of Mucin-2, occludin, ZO1, claudin-1, TNF-α, IL-6, IL-1β, IL-10, IL-4, Bax, Bcl-2, SOD1 and GPx-2. The levels of SOD, GPX, CAT and MDA. Total antioxidant capacity assay. | Quercetin and vitamin E improve intestinal function in aged breeder hens by protecting intestinal structure and integrity. | [212] | |
| Vitamin K and vitamin D | Human osteoblasts cultured in presence of hydroxyapatite-based biomaterials | Cell viability assay; ROS and GSH level assay; GPX and ALP activity; DNA proliferation assay. | Vitamins D and K protect redox balance and support growth of osteoblasts affected by hydroxyapatite-based biomaterials due to antioxidant properties. | [213] | |
| Vitamin K2 | Wild-type and mutant-type C. elegans | Longevity and survival assay; RNA-sequencing analysis; Progeny and reproductive activity assay; Expression of daf-12, fard-1, fat-5/6/7, and lipl-4. | Vitamin K2 extends the lifespan of C. elegans and improves the resistance to pathogen infection, heat stress and H2O2-induced inner oxidative stress by enhancing fat metabolism. | [214] |
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Song, L.; Zhang, S. Anti-Aging Activity and Modes of Action of Compounds from Natural Food Sources. Biomolecules 2023, 13, 1600. https://doi.org/10.3390/biom13111600
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Song L, Zhang S. Anti-Aging Activity and Modes of Action of Compounds from Natural Food Sources. Biomolecules. 2023; 13(11):1600. https://doi.org/10.3390/biom13111600
Chicago/Turabian StyleSong, Lili, and Shicui Zhang. 2023. "Anti-Aging Activity and Modes of Action of Compounds from Natural Food Sources" Biomolecules 13, no. 11: 1600. https://doi.org/10.3390/biom13111600
APA StyleSong, L., & Zhang, S. (2023). Anti-Aging Activity and Modes of Action of Compounds from Natural Food Sources. Biomolecules, 13(11), 1600. https://doi.org/10.3390/biom13111600
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