Next Article in Journal
Chiral Switch: Between Therapeutical Benefit and Marketing Strategy
Previous Article in Journal
The Evolution of Pharmacological Activities Bouea macrophylla Griffith In Vivo and In Vitro Study: A Review
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Black Elder and Its Constituents: Molecular Mechanisms of Action Associated with Female Reproduction

by
Adriana Kolesarova
1,*,
Simona Baldovska
2,
Ladislav Kohut
1 and
Alexander V. Sirotkin
3
1
Institute of Applied Biology, Faculty of Biotechnology and Food Sciences, Slovak University of Agriculture in Nitra, 949 76 Nitra, Slovakia
2
AgroBioTech Research Centre, Slovak University of Agriculture in Nitra, 949 76 Nitra, Slovakia
3
Department of Zoology and Anthropology, Faculty of Natural Sciences, Constantine the Philosopher University in Nitra, 949 01 Nitra, Slovakia
*
Author to whom correspondence should be addressed.
Pharmaceuticals 2022, 15(2), 239; https://doi.org/10.3390/ph15020239
Submission received: 18 January 2022 / Revised: 15 February 2022 / Accepted: 15 February 2022 / Published: 17 February 2022
(This article belongs to the Section Pharmacology)

Abstract

:
The present review summarizes the current knowledge concerning provenance, properties, physiological and therapeutic actions of elderberry and the bioactive molecules present in the plant, with emphasis on their action on female reproduction. Elderberry or black elder (Sambucus nigra L.) attracts attention due to its easy cultivation and high availability of bioactive compounds. Most of the available data concerning black elder’s therapeutic action are focused on its effects such as activation of immune processes and anti-inflammatory processes (cytokine production, etc.) and regulation of hormones and their receptors in cancer cells. The effects of elderberry on reproduction have been poorly investigated so far. Nevertheless, conducted studies so far demonstrate the stimulatory influence of black elder extract and its constituents, such as rutin, anthocyanins and agglutinins, on the viability and steroidogenesis of healthy ovarian cells as well as their ability to promote apoptosis and reduce the viability and proliferation of ovarian cancer cells. Furthermore, the action of black elder extract and its constituent biomolecules, such as anthocyanins and lectins, on embryogenesis and the embryonal estradiol-estradiol receptor system have also been reported. The available information, despite limitations, suggest the applicability of black elder constituents for improvement of reproductive processes in animal biotechnology, animal production and assisted reproduction, as well as for prevention and treatment of reproductive disorders (including cancer) in veterinary and human medicine.

1. Introduction

The search for new regulators of reproduction is important for the solution of various problems of modern society. Intensive animal production is associated with growing incidences of farm animal infertility [1]. The occurrence of reproductive disorders is currently growing in all mammalian species [2]. The inability to have children affects 10% to 20% of all couples in the modern world, which promotes the development of reproductive medicine and assisted reproduction. Subfertility affects many more people [3,4,5]. Moreover, gynecological cancers are the key cause of mortality in women [6]. Biotechnology in animal production (from artificial insemination to generation of transgenic organisms) is focused on reproductive processes; therefore, its development requires a search for new regulators and medicines affecting these processes [7].
The majority of reproductive dysfunctions have similar causes and mechanisms—the ability of various adverse environmental factors to induce oxidative stress—including the accumulation of reactive oxygen species, which are deleterious to DNA and proteins, ovarian folliculogenesis and embryogenesis. Oxidative stress can be prevented by antioxidants [4]. The most natural, accessible and inexpensive sources of antioxidants, which can affect reproductive processes and prevent numerous reproductive disorders, are plants [6,8]. Additionally, because of implications on health, there is a growing interest in the use of plant-based antioxidants in the food industry. In this regard, replacing synthetic additives with natural bioactive compounds extracted from plants has been an important strategy for food manufacturers [9,10,11].
One of the promising and widely accessible sources of antioxidants and other biologically active substances affecting reproductive and non-reproductive processes and health could be the black elderberry (Sambucus nigra L.). Due to its health-promoting and sensory properties, elderberry is used primarily in the food and pharmaceutical industries [12]. The popularity of this plant among food and pharma producers is growing due to its simple cultivation, high availability and high number and quantity of bioactive compounds with physiological and therapeutic properties [10,13].

2. Provenance and Properties

Black elderberry belongs to the Adoxaceae family, and its common names are elder, elderberry, black elder, European elder, European elderberry, and European black elderberry [14]. Sambucus nigra is a small tree or shrub, 1–8 m tall with a strong odor. The bark is brownish, with longitudinal fractures and deep grooves. The leaves are opposite, imparipinnate, with 5–7 elliptic-lanceolate, dentate leaflets. The inflorescence is an umbel with many milky-white flowers. The fruit is a shiny black-purple color, with a subspherical drupe. The plant is found in woods, clearings and hedges from sea level to mountainous elevations [15].
Black elderberry is an extremely accessible and abundant plant native to the Northern hemisphere. Their seeds are spread rapidly by birds and other animals to colonize forest edges and disturbed areas and are nowadays diffused in various habitats including subtropical regions of Asia, North Africa and North America [12,16,17]. Since the beginning of 1980s, black elderberry has been planted and commercialized in some countries in Europe, the USA, Canada, New Zealand and Chile [16]. In Europe, elderberries have been intensively used for centuries both in the food industry to produce pies, jellies, jams, ice creams, yogurts and different alcoholic beverages [17], and in folk medicines for treatment of various diseases and ailments due to their antioxidant, anticarcinogenic, immune-stimulating, antiallergic, antiviral and antibacterial properties [18]. These aspects of elderberry have recently received significant attention, especially for antioxidant capacity, as functional compounds in food applications such as natural conservatives or food supplements [19].
All parts of this plant (flower, bark, leaf and fruits) are rich sources of dietary phytochemicals, such as carbohydrates, lipids, terpenoids, flavonoids, phenolic acids, alkaloids, etc. [16,20]. The content of the essential fatty acids, such as linoleic and α-linolenic acids, is very high (approximately 39% each), and the polyunsaturated fatty acids represent 78% of the total fatty acids. The most prominent compounds present in black elderberry fruits are polyphenols, e.g., anthocyanins, with high antioxidant capacity. The major elderberry anthocyanins are cyanidin-3-glucoside and cyanidin-3-sambubioside, which are found in elderberry juice and polar extracts [21,22,23]. In addition, elderberries are a rich source of flavanols, phenolic acids and procyanidins. Elderflowers are particularly rich in flavonoids (up to 3%), such as kaempferol, astragalin, quercetin, quercetin-3-O-glucoside, rutin, isoquercitrin and hyperoside, as well as phenolic acids, gallic acid and gentisic acid [9,23,24]. The most abundant polyphenol in elderflower is the flavonoid rutin [25]. Our screening of elderflower extract confirmed that this plant represents a rich source of polyphenols, and the most prominent compound present in elderberry extracts from flowers and berries was the flavonoid rutin [26]. Additionally, other types of polyphenols like flavonol glycosides and flavonol esters are present in elderberries [27]. Other known biologically active substances in elderberry include lectins, especially agglutinins, cyanogenic glycosides, essential oils, fatty acids, organic acids, carbohydrates, vitamins and minerals [12,28,29,30,31,32,33]. Every 100 g serving of fresh berries contains vitamin B2 (65 mg), vitamin B6 (0.25 mg), vitamin C (18–26 mg), folic acid (17 mg), biotin (1.8 mg), β-carotene (0.36 mg), pantothenic acid (0.18 mg), nicotinamide (1.48 mg), potassium (288–305 mg), phosphor (49–57 mg), pectin (0.16%) and glucose and fructose (7.5%) [34].
The characteristic aroma of elderberries is a result of (E)-β-damascenone, dihydroedulan, ethyl-9-decenoate, 2-phenyl ethanol, phenylacetaldehyde and nonanal. Alcohols, esters and aldehydes are frequently identified volatile groups in elderberries. Other major secondary metabolites comprise approximately 1% triterpenes (as α- and β-amyrin, ursolic acid and oleanolic acid) and about 1% sterols (β-sitosterol, campesterol and stigmasterol). In addition, pectins, tannins and phenolic acids are found in the flowers [35,36]. Elderflowers have a strong, flowery, pleasant odor mainly due to the presence of 0.03–0.14% of essential oils. In addition, the aroma composition of elderflowers includes aldehydes, ketones, alcohols, esters, oxides, terpenes and free fatty acids [37]. The bark, leaves, seeds and raw or unripe fruits contain the cyanogenic glycoside sambunigrin, which is potentially toxic because it can release cyanide [23,38,39].
Therefore, various parts of the elderberry plant demonstrate the presence of high amounts of biologically active molecules with a wide spectrum of effects—from antioxidative and phytoestrogenic polyphenols to toxic aldehydes and glycosides. The presence of these molecules could explain the physiological and therapeutic effects of this plant, as well as the variability in its action on different targets listed below.

3. Physiological and Therapeutic Actions of Elderberry and Its Constituents

Elderberry is widely used in folk medicine through its pharmacological properties [40]. Currently, it presents as one of the most used medicinal plants worldwide [41]. In folk medicine, elderberry is used in the treatment of many diseases and ailments thanks to its antioxidant, anticarcinogenic, immune stimulating, antiallergic, antiviral, antibacterial [12,18,28], antidepressant and hypoglycemic properties, as well as the ability to reduce body fat and blood lipid concentrations [12]. Elderberry flowers can be used both for prevention and therapy of a wide array of diseases due to immunomodulatory [42,43], anti-inflammatory [44,45,46], antioxidant [28,47,48,49,50], antimicrobial [12,51,52] and antiviral [41,53,54] activities. In vitro experiments demonstrated the ability of elderberry extract or its constituents to suppress proliferation and viability of various cancer cell lines [25,33,55,56,57,58] and to prevent angiogenesis in tumor [55,59]. On the other hand, in some cases (estrogenic breast cancer cells and osteosarcoma cells), the biomolecule rutin found in the black elderberry did not affect cancer cell viability [60]. However, it could improve the acetic acid-induced colitis [28]. There are some reports on the neuromodulatory, particularly anticonvulsant [61] and analgesic [28,62], effects of elderberry extracts. In rats, this extract induced central depression [28], but experiments on mice showed its antidepressant activities [63].
Elderflowers have been used in traditional medicines for the management of inflammation, skin disorders such as diuretic, colds, fevers and other respiratory disturbances [28,64,65]. For example, it has the potential to ameliorate skin photoaging and inflammation [66]. Elderberry extract inhibited the infectious bronchitis virus at an early point during replication [67,68,69]. Consumption of elderberry extract has also been suggested for people with diabetic osteoporosis for improving lipid profile and reducing atherogenic risk and hyperglycemia [70]. In vitro studies suggested that elderflower extracts stimulate insulin-dependent glucose uptake [71,72,73]. It can improve functions of the cardiovascular system, improve exercise performance and mitigate the risk of cardiovascular diseases [62]. Elderberry anthocyanins can be efficient against atherosclerosis and Helicobacter pylori, a noxious pathogen responsible for various gastrointestinal disorders including duodenal ulcer and gastric cancer [55]. There is evidence for the applicability of black elderberry for the treatment of obesity [74,75]. Recently, elderberry has received significant attention from food producers due to its applicability as a natural food conservator [19]. For better visualization of the physiological and therapeutic actions of elderberry, we summarize in vitro and in vivo studies, elderberry preparation, experimental models and effects observed in Table 1.
No substantial adverse side effects of black elderberry have been reported so far [23]. Moreover, there are a growing number of reports concerning the physiological and curative actions of elderberry. Nevertheless, the majority of these effects were shown only on limited numbers of animals or in vitro experiments, whilst clinical trials are rare. Sometimes the effect of elderberry was influenced by the kind of its extract (aqueous or ethanol), indicating the influence of solvent itself or that different solvents are extracting different plant molecules [28]. The hierarchical interrelationships (primary and secondary effects) are possible; for example, the anti-obesity and antidiabetic effects of elderberry could be explained by its stimulatory action on glucose uptake and fat metabolism.

4. Mechanisms of Action of Elderberry and Its Constituents

4.1. Constituents Responsible for Particular Effects of Elderberry

It is widely accepted that elderberries’ curative capacity is due to the presence of high amounts of polyphenolic compounds, primarily flavonols, phenolic acids and anthocyanins. The presence of polyphenols, which assure the defense of plants against pathogenic microorganisms, can also explain the ability of black elderberry to suppress the activity of viruses [41,53,54] and bacteria in the body [12,51,52] and in food items [19].
Plant polyphenols are known free radical scavengers and are able to protect the human body against oxidative stress and peroxidative processes [62,76,77,78]. The strong antioxidant capacity of elderberries is probably related to the most abundant and biologically active flavonols rutin and quercetin, as well as to gallic acids [79]. Rutin (the most abundant polyphenol in elderflower) was found to inhibit the viability of human neuroblastoma [25], leukemic [56] and breast cancer [57] cells. Therefore, the anticancer activity of black elderberry can be due to the presence of rutin. On the other hand, the ability of elderberries’ anthocyanins to suppress malignant transformation of endothelioma cells has also been demonstrated [55,80]. These reports suggest the anticancer effects of several elderberry polyphenols, which could act as synergists.
There is evidence that the positive action of elderberry on vascular health is due to the presence of anthocyanins, especially cyanidin-3-O-glucoside [59,62]. Moreover, elderberry agglutinins can selectively bind to apoptotic cells, and can be involved in the execution of mitochondrial apoptosis in various cell types [81]. Finally, elderberry agglutinin can block vascular endothelial growth factor (VEGF)-induced angiogenesis [82], which plays an important role in tumor growth. These observations indicate that the pro-apoptotic action of elderberry could be due to the presence of agglutinins. The elderberry constituents responsible for other effects of this plant remain to be identified yet.
It may, however, be noted that search for an active compound of any plant, including elderberry, is difficult because the tested commercial and non-commercial dietary supplements usually contain multiple ingredients. In addition, substantial differences are often found between labelled and actual ingredients or their amounts [23]. Furthermore, the hypothesis concerning active components of elderberry, which are responsible for a particular effect, is based usually on a similarity of the whole plant extract’s effect and its putative constituent(s). To our knowledge, the effect of the elderberry extract and the effect of its constituents have not been compared in a single experiment yet.

4.2. Mediators of Effects of Elderberry and Its Constituents

As mentioned above, several curative effects of elderberry could be explained by high contents of antioxidants, which can either directly eliminate free oxygen species or promote antioxidative enzymes within the cells [62,76,77,78]. Mitigation of oxidative stress and protection of genomic DNA integrity are probably the main mechanisms of elderberry’s inhibitory action on carcinogenesis, blood vessels, brain functions, inflammatory and gut microbiota [55,80], skin aging and inflammation [66].
Furthermore, the antioxidative and anticancer effects of elderberry anthocyanins are associated with the downregulation of promoters and markers of inflammation, such as monocyte chemoattractant protein-1 (MCP-1), transcription factor nuclear factor kappa B (NF-κB) and interleukin 8 (IL-8). Some similar signaling substances were changed during curative elderberry action on skin photoaging and inflammation. This effect was associated with a decrease in matrix metalloproteinase-1 (MMP-1) expression, secretion of inflammatory cytokines, mitogen-activated protein kinases/activator protein 1 (MAPK/AP-1) and NF-κB signaling pathways and skin inflammation. In addition, elderberry extract improved nuclear factor E2-related factor 2/heme oxygenase-1 (Nrf2/HO-1) signaling to increase oxidative defense capacity, enhanced transforming growth factor beta (TGF-β) signaling activation to promote procollagen type I synthesis and blocked extracellular matrix degradation [66].
The protective effect of elderberry flavonoids and pectins against the influenza virus is probably mediated by stimulating the immune system of the host through enhancing the production of inflammatory cytokines such as interleukins IL-6, IL-8 and tumor necrosis factor (TNF) [54,68,83] and the subsequent stimulation of macrophages [84]. Therefore, elderberry antioxidants could protect the target tissues via reduction of oxidative stress and the downregulation of regulators of inflammatory processes.
In addition, black elderberry anthocyanins can improve vascular health by promoting the production of nitric oxide, which in turn promotes vascular permeability and vasodilation and reduces blood pressure [62]. On the other hand, tumor anthocyanin cyanidin-3-glucoside can suppress angiogenesis via the downregulation of production of VEGF and STAT-3, a post-receptor mediator of VEGF action on vascular development [59]. Elderberry lectins can downregulate angiogenesis via a blockade of VEGF receptors [82].
Finally, elderberry can influence some physiological processes via changes in steroid hormones and their receptors. Elderflower extracts promoted estradiol release, downregulated estrogen receptor alpha and upregulated progesterone receptor expression in cultured breast cancer cells, which are involved in the control of cell proliferation [57]. The endocrine effects of elderflower could be due to phytoestrogen activity of several elderberry polyphenols, i.e., their ability to bind steroid hormone receptors and to affect the release of steroid hormones and hormone-dependent events [85].
Taken together, the available data suggest that the non-reproductive effects of black elderberry are mediated by changes in oxidative, inflammatory, and regenerative processes, as well as angiogenesis, steroid hormones and their receptors. The functional interrelationships between these processes are possible. At least, the influence of oxidative stress and antioxidants on inflammatory processes, which in turn trigger cancerogenesis/carcinogenesis, has been suggested [86]. Furthermore, the adverse effects of oxidative stress on steroidogenesis and nitric oxide have been documented [87,88]. Nevertheless, the functional interrelationships between particular signaling pathways mediating elderberry actions require further elucidation. Furthermore, various elderberry constituents could affect different targets via several mediators—this hypothesis, however, requires validation by further studies.

5. Effects of Elderberry and Its Constituents on Female Reproductive Processes

5.1. Effect of Elderberry and Its Constituents on Ovarian Cell Viability, Apoptosis and Proliferation

Our recent in vitro study demonstrated the promising stimulatory effect of elder-berry extracts on the viability of human ovarian granulosa cells [26]. This in vitro study indicated an increase in the number of viable ovarian cells after the addition of the ex-tracts from different parts of the elderberry plant (flowers and berries).
The role of a particular elderberry molecule responsible for its effect could be detected by comparison of the effects of the whole elderberry extract and its particular constituents. The most known biologically active constituents of elderberry are rutin, anthocyanins and agglutinins. The most abundant polyphenol in elderflower and elderberry is the flavonoid rutin [25,26]. The comparison of the effects of elderberry extract and rutin showed the similar effects for the extracts and its major component. In experiments of Sirotkin et al. [8,89], the addition of rutin was found to increase the viability of cultured porcine ovarian granulosa cells, although this effect was not associated with changes in the accumulation of markers of proliferation (accumulation of PCNA) and cytoplasmic apoptosis (Bax). In vivo experiments, like in vitro ones, demonstrated the stimulatory action of rutin on rat ovarian cell health and ovarian folliculogenesis [90,91].
In contrast to healthy ovarian cells, in the case of cultured cancer cells, native and hydrolyzed rutin exerted in vitro inhibitory activity against human ovarian adenocarcinomas by suppression of the viability and proliferation of OVCAR-3 ovarian carcinoma cells [92,93]. Additionally, the viability and proliferation of ovarian cancer cells were reduced by other elderberry constituents such as anthocyanins [94], glycosylated cyanidin derivatives [95] and delphinidin [96]. Another elderberry constituent, agglutinins, was reported to reduce viability and mitochondrial activity and also induce apoptosis of cultured ovarian cancer cells [33].
The present observations suggest the stimulatory influence of black elderberry substances on the viability of healthy ovarian cells and the ability of elderberry to promote apoptosis and reduce the viability of cultured ovarian cancer cells. These phenomena suggest that this plant can be principally useful for stimulation of healthy ovarian cells and suppression of cancer ovarian cell functions. The comparison of the action of elderberry and its constituents indicates that its action on ovarian cell viability and proliferation can be due to the presence of rutin, anthocyanins and/or agglutinins.

5.2. Effect of Elderberry and Its Constituents on Ovarian Cell Steroidogenesis

Our recent study demonstrated the influence of both elderberry extracts from dark purple elderberry fruits, as well as from elderflowers on steroid hormone release by cultured human granulosa cells. The release of both progesterone and 17ß-estradiol by the cells was increased after supplementation by either elderflower extract or extract from the berries of the shrub. The results of this study demonstrated the benefits of elderberry extracts prepared from different parts of plant (flowers and fruits) in the upregulation of biosynthesis of ovarian steroid hormones in vitro [26].
According to the above-mentioned hypothesis, the black elder constituents responsible for the elderberry’s effects on ovarian steroidogenesis are to be suggested on the basis of the similarity of effects. Such similarity in elderberry and rutin has been reported. In vivo and in vitro studies on rats demonstrated the ability of rutin to promote the plasma luteinizing hormone (LH) level, expression of ovarian follicle-stimulating hormone (FSH) receptors, steroidogenic enzymes, ovarian folliculogenesis and fecundity [90,91]. In in vitro experiments with cultured porcine granulosa cells, the addition of rutin was able to promote 17β-estradiol and testosterone, but not progesterone release [8,89,97]. It is not to be excluded that the increase in granulosa cell viability under the influence of elderberry extract could be due to the upregulation of estradiol, a known promoter of ovarian cell viability and ovarian folliculogenesis [98].
The current literature does not portray evidence concerning anthocyanins’ action on ovarian steroidogenesis, although the phytoestrogenic effects of anthocyanins, especially of cyanidin and delphinidin, have been reported [99,100]. The high dietary consumption of anthocyanins by humans was associated with a lower level of plasma dehydroepiandrosterone, but not of progesterone, androgens and estrogens [101]. The stimulatory action of anthocyanin cyanidin-3-O-glucoside on FSH, LH receptors and testosterone production by mice testis has been shown [102], but similar experiments on females have not been reported.
Again, the current literature does not demonstrate the changes in ovarian steroidogenesis under influence of agglutinins. Therefore, there is no evidence so far that elderberry action on ovarian steroid hormones could be due to anthocyanins or agglutinins. On the other hand, the high similarity in stimulatory action of elderberry extract and rutin on healthy granulosa cell viability and steroidogenesis suggests that plant action on ovarian cells can be due to the presence of the most abundant plant flavonol rutin. Furthermore, the steroid-promoting effect of elderberry indicates the potential applicability of this plant and its constituent rutin for the promotion of steroid-dependent non-reproductive and reproductive events including ovarian folliculogenesis and fecundity.

5.3. Effect of Elderberry and Its Constituents on Embryo

Schröder et al. [57] did not find any effect of elderflower extract on the proliferation of human embryonal trophoblast cancer cells. This observation is in line with the absence of action of the main elderberry constituent rutin on the embryogenesis of Xenopus laevis [103] or on the viability of cultured human lung embryonic fibroblasts and human umbilical vein endothelial cells [104]. Therefore, the influence of elderflower or its constituent rutin on embryonal cells has not been detected yet.
Other black elder constituents, such as anthocyanins [105], and here especially cyanidin (but not kuromanin) [106], were able to improve the quality and developmental capacity of porcine embryos indicating the stimulatory action of elderberry anthocyanins on embryogenesis. A similar ability to increase the viability of chicken embryonal fibroblast cells was reported for another anthocyanin, the nightshade anthocyanin [107].
In contrast to elderberry anthocyanin, elderberry lectins blocked receptors of vascular endothelial growth factor (VEGF) in embryonal tissue, which is responsible for embryonal angiogenesis (endothelial cell proliferation and motility) [82]. These data indicate the stimulatory action of black elderberry anthocyanin and the adverse effect of its lectins on embryogenesis.
Schröder et al. [57] also studied the effect of elderflower extracts on the production of estradiol and estrogen receptors alpha (ER-α) using trophoblast tumor cell lines JEG-3 and BeWo. Elderflower extracts inhibited estradiol production in JEG-3 cells and prompted in BeWo cells. Furthermore, it upregulated the accumulation of estradiol receptors in JEG-3 cell lines. These observations demonstrate that black elderberry extract can affect embryonal trophoblast and its estradiol-estrogen receptor system, which could be responsible for embryo development and maintenance of gravidity. Furthermore, it indicates the black elderberry’s influence on trophoblast cancerogenesis.
Therefore, the available publications indicate both stimulatory and inhibitory actions of elderberry extract and its constituents rutin, anthocyanins and lectins on regulators of embryogenesis, embryonal cancerogenesis and steroidogenesis. The ability of steroid hormones to promote both embryo development [108] and malignant transformation [109] is well-known. Therefore, the influence of elderberry molecules’ action on embryo and cancerogenesis through the estrogen/estrogen receptor system could be proposed. Nevertheless, understanding such interrelationships, causes in variability in elderberry molecules on various embryonal targets, their biological significance and practical applicability requires further profound studies.

6. Extracellular Mechanisms of Action of Elderberry and Its Constituents on Female Reproductive Processes

Although numerous signaling pathways are involved in elderberry action on non-reproductive processes, research enabled the identification of only some pathways mediating the effect of black elderberry on reproduction, and less studies have been performed to detect mediators of this plant’s action on female reproductive processes.
The direct action of the elderberry extract on reproductive organs and the ability to affect cultured ovarian [26] and embryonal trophoblast [57] cells was demonstrated. Moreover, the elderberry constituents, such as rutin [8,89,92,93], anthocyanins [94,95,96], and agglutinins [33] directly influence the viability, proliferation and apoptosis of ovarian cells.
The ability of elderberry constituents rutin [90,91] and anthocyanins [102] on LH and FSH release indicate that they could regulate reproductive functions through the upregulation of pituitary gonadotropins. The ability of rutin to affect ovarian gonadotropin receptors [90,91] indicates that these receptors could be the next mediators of elderberry action on the ovary.
Elderberry extract affected steroid hormones release by ovarian granulosa cells [26] and embryonal trophoblast cells [57]. The influence of elderberry molecule rutin [90,91], but not of anthocyanins and agglutinins, on ovarian steroidogenesis has also been reported. These observations suggest that steroid hormones could be one of the mediators of the black elderberry and its molecule rutin on ovarian functions, and so can promote ovarian cell viability through the stimulation of steroidogenesis [98]. Finally, the influence of elderberry extract on embryonal cancer cell estrogen/estrogen receptor systems [57], as well as the importance of this system in control of embryogenesis [108] and cancerogenesis [109], indicate that elderberry can affect embryos via estrogens and its receptors. Nevertheless, such hypotheses require direct experimental confirmation.

7. Intracellular Mechanisms of Action of Elderberry and Its Constituents on Female Reproductive Processes

The current literature does not contain evidence concerning the intracellular mechanisms of the whole elderberry extract action on ovarian cells; however, there are some reports concerning the key elderberry constituents (rutin, anthocyanins, agglutinins) on cultured ovarian cells and cancer cells, which could help to understand the mediators of elderberry actions on either healthy or malignant cells.
Treatment of mice with rutin boosted ovarian follicular health and ovarian cell proliferation, increased the number of active mitochondria and the intracellular level of the antioxidant glutathione, reduced ovarian cell ROS level and markers of apoptosis (PTEN/FOXO3a) pathway and mitigated the toxic effect of cisplatin on ovarian functions [110].
The other elderberry constituents, namely anthocyanins [105] including cyanidin [106] and nightshade anthocyanin [107], activated antioxidant enzymes and reduced the contents of ROS in embryonal cells. These changes were associated with improvement of embryo quality and viability [105,106]. These reports suggest that elderberry anthocyanins can boost embryo viability via the elimination of ROS-induced oxidative stress. In cultured cancer cells, another elderberry anthocyanin, delphinidin, was able to decrease the intracellular level of ATP, changed the intracellular amount of ROS and antioxidant glutathione and decreased the mitochondrial membrane potential and mitochondrial mass indicating oxidative stress-induced apoptosis [111]. In addition, delphinidin can suppress proliferation and migration of ovarian cell carcinoma cells through blocking AKT and ERK1/2 MAPK signaling pathways [96]. On the other hand, anthocyanidins possess weak phytoestrogenic properties [99,100]. Due to these properties, they could promote proliferation of estrogen-dependent cancer cells [99].
A similar mechanism of action on ovarian cancer cells was reported for black elderberry agglutinin. Chowdhury et al. [33] demonstrated that the suppressive action of the black elderberry constituent on ovarian cancer cells is mediated by a cascade of events:
(1)
Black elderberry agglutinin activates the signaling pathways of AKT and ERK1/2, which promotes de-phosphorylation of dynamin-related protein-1 (Drp-1).
(2)
Upon its translocation to the mitochondrial fission loci, Drp-1 induces fragmentation of the mitochondrial membrane.
(3)
Mitochondrial outer membrane permeabilization results in the generation of ROS and cytochrome-c release into the cytosol—the signs of mitochondrial apoptosis.
(4)
These changes may result in cell cycle arrest before the G2/M phase and programmed cell death.
Results of the study also demonstrated that black elderberry and its constituent rutin could promote healthy ovarian cell functions through the upregulation of gonadotropins, gonadotropin receptors, steroid hormones, antioxidants, reduction in oxidative stress and apoptosis, which in turn improves ovarian cell viability and fecundity. In contrast, in the case of ovarian cancer cells, elderberry and its constituents, rutin, anthocyanins and agglutinin, can suppress cell viability and functions via the downregulation of the similar mechanisms—AKT- and ERK1/2-dependent intracellular signaling pathways—promoters of cell proliferation and by induction of ROS-induced cytoplasmic/mitochondrial apoptosis. Understanding the causes of opposite action of elderberry and its molecules on healthy and cancer ovarian cells via similar intracellular mechanisms require further studies. Such studies could be helpful for possible application of elderberry for stimulation of healthy ovary and reproductive processes and suppression of ovarian cancer (see below). Available evidence concerning the possible regulators of female reproductive processes affected by black elderberry and its constituents are summarized in Figure 1.

8. Application in Reproductive Biology and Medicine

The reported effects of black elderberry and its constituents on female reproductive processes summarized here indicate that these plant preparations could be stimulators of healthy ovarian cells and embryogenesis. It is not to be excluded that these preparations can support ovarian folliculogenesis, oogenesis, fecundity, embryogenesis and gravidity, to relieve the age-related reproductive insufficiency and menopause-related problems. As promoters of release and reception of gonadotropins and steroid hormones, as well as phytoestrogens, they could be useful in veterinary and human medicine for the treatment of disorders induced by a deficit of these hormones—age-related reproductive insufficiency, menopause-related problems, osteoporosis and polycystic ovarian syndrome. The ability of elderberry and its molecules to promote reproductive processes and fecundity could be useful in the induction of ovulation and superovulation in biotechnology in animal production and assisted reproduction. On the other hand, the ability of black elderberry substances to downregulate cell proliferation and viability of ovarian and trophoblast tumor cells indicates the potential ability of these substances for prevention, mitigation and treatment of ovarian and embryonal cancers.
Efficiency of elderberry’s polyphenols could be increased by search of its safe and effective dosage, and the improvement of its stability, bioavailability and delivery by using nano-emulsion and nanoliposome systems, which can enhance the biological and therapeutic activity of these plant molecules [74,112].
Analysis of the available literature performed here shows that black elderberry contains several biologically active substances with different, sometimes opposite, actions. Some elderberry constituents could be toxic (see Section 2). Some other elderberry constituents have different chemical structures, but similar mechanisms of action (see Section 4, Section 6 and Section 7). On the other hand, the substantial differences in character, targets (see Section 5) and mechanisms of action (see Section 6 and Section 7) of various elderberry substances have been demonstrated. These facts indicate that the application of pure elderberry constituents with defined contents, amounts and effects could be more specific, controllable and efficient than the use of the whole crude plant extract. The published reports indicate that among the identified black elderberry constituents, rutin, anthocyanins (especially cyanidin-3-O-glucoside) and agglutinins could be molecules that are the most active and promising as both stimulators of reproductive functions and inhibitors of ovarian cancer. Both rutin and anthocyanins can promote gonadotropin release and reception, as well as promote ovarian cell functions. It is possible that these substances could be potentially useful as additives to gonadotropins for induction of ovarian folliculogenesis and the induction of ovulation and superovulation in animal biotechnology, assisted reproduction and medicine. On the other hand, only anthocyanins, but not rutin or agglutinins, were able to support embryogenesis. It is possible that anthocyanins could be applicable as additives to the culture medium for improvement of embryo development in in vitro embryo production. All the three mentioned elderberry constituents were shown to possess anticancer activity, and therefore all three preparations possess the potential to be useful in the management of ovarian cancer. Nevertheless, the number of reported studies is too modest to make a definite conclusion concerning elderberry constituent most suitable for particular biomedical applications.

9. Conclusions and Possible Direction of Future Studies

The reproductive effects of black elderberry extract and its constituents have been investigated insufficiently. Nevertheless, the published reports demonstrate the stimulatory influence of black elderberry extract and its constituents—rutin, anthocyanins and agglutinin—on steroid hormones and their receptors in ovarian and embryonal cells. The stimulatory influence of anthocyanins on embryogenesis has also been reported. On the other hand, rutin, anthocyanins and agglutinins can suppress ovarian and embryonal cancer cell functions. The effects of black elderberry and its molecules could be mediated by intracellular signaling pathways regulating cell proliferation, oxidative processes, cytoplasmic/mitochondrial apoptosis and viability, as well as by estrogen and estrogen receptors and angiogenesis. The available evidence indicates the potential usefulness of black elderberry extract and its constituents rutin and anthocyanins as biostimulators of female reproductive processes, as well as the potential applicability of whole elderberry extract, with rutin, anthocyanins and agglutinins, for the treatment of ovarian cancer and other reproductive disorders in animal biotechnology, animal production, assisted reproduction and veterinary and human medicine.
Nevertheless, the current state-of-art research invokes more queries concerning black elderberry action on female reproduction than answers. All biologically active constituents of black elderberry remain to be identified, and their biological activity remains to be investigated. The action of black elderberry extract has not been studied in in vivo experiments, whilst the reproductive effects of elderberry constituents were studied mainly in in vitro experiments and in a few animal studies. Adequate clinical studies have not been reported yet. Moreover, characteristics and mechanisms of action and biological activities of several elderberry constituents have not been compared in the same experiments yet. The conclusions concerning mechanisms of action of elderberry and its molecules are made mainly based on observations of changes in some signaling molecules after treatment, but the physiological role and functional interrelationships between particular signaling molecules remain rather hypothetical. Therefore, although the influence of black elderberry and its constituents on female reproductive processes has been demonstrated, its actions and potential applications require further studies.

Author Contributions

Conceptualization, A.K. and A.V.S.; methodology, A.K.; software, A.K.; validation, A.K., S.B. and A.V.S.; formal analysis, A.V.S.; investigation, A.K., S.B., L.K. and A.V.S.; resources, L.K.; writing—original draft preparation, A.K. and S.B.; writing—review and editing, A.K. and A.V.S.; visualization, S.B.; supervision, A.K.; project administration, A.K.; funding acquisition, A.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Ministry of Education, Science, Research and Sport of the Slovak Republic projects APVV-18-0312, DS-FR-19-0049, VEGA 1/0266/20, KEGA 033SPU-4/2021, the Operational Programme Integrated Infrastructure within the project: Demand-driven research for the sustainable and innovative food, Drive4SIFood 313011V336, co-financed by the European Regional Development Fund, and ERASMUS+ Programme of the European Union KA2 2020-1-SK01-KA203-078363.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Acknowledgments

The authors thank Shubhadeep Roychoudhury for language editing and proofreading and the excellent scientific team “Center of Animal Reproduction (CeRA)” for their support.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Mee, J.F. Reproductive issues arising from different management systems in the dairy industry. Reprod. Domest. Anim. 2012, 47, 42–50. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Canipari, R.; De Santis, L.; Cecconi, S. Female Fertility and Environmental Pollution. Int. J. Env. Res. Public Health 2020, 17, 8802. [Google Scholar] [CrossRef]
  3. Roudebush, W.E.; Kivens, W.J.; Mattke, J.M. Biomarkers of Ovarian Reserve. Biomark. Insights 2008, 3, 259–268. [Google Scholar] [CrossRef] [Green Version]
  4. Wojsiat, J.; Korczyński, J.; Borowiecka, M.; Żbikowska, H.M. The role of oxidative stress in female infertility and in vitro fertilization. Postepy Hig. Med. Dosw. 2017, 71, 359–366. [Google Scholar] [CrossRef]
  5. Smits, R.M.; Mackenzie-Proctor, R.; Fleischer, K.; Showell, M.G. Antioxidants in fertility: Impact on male and female reproductive outcomes. Fertil. Steril. 2018, 110, 578–580. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Akkol, E.K.; Dereli, F.T.G.; Sobarzo-Sánchez, E.; Khan, H. Roles of Medicinal Plants and Constituents in Gynecological Cancer Therapy: Current Literature and Future Directions. Curr. Top. Med. Chem. 2020, 20, 1772–1790. [Google Scholar] [CrossRef] [PubMed]
  7. Sirard, M.A. 40 years of bovine IVF in the new genomic selection context. Reproduction 2018, 156, R1–R7. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Sirotkin, A.; Záhoranska, Z.; Tarko, A.; Fabova, Z.; Alwasel, S.; Halim Harrath, A. Plant polyphenols can directly affect ovarian cell functions and modify toluene effects. J. Anim. Physiol. Anim. Nutr. 2021, 105, 80–89. [Google Scholar] [CrossRef]
  9. Domínguez, R.; Zhang, L.; Rocchetti, G.; Lucini, L.; Pateiro, M.; Munekata, P.E.S.; Lorenzo José, M. Elderberry (Sambucus nigra L.) as potential source of antioxidants. Characterization, optimization of extraction parameters and bioactive properties. Food Chem. 2020, 330, 127266. [Google Scholar] [CrossRef]
  10. Lorenzo, J.M.M.; Pateiro, M.; Domínguez, R.; Barba, F.J.; Putnik, P.; Kovačević, D.B.; Franco, D. Berries extracts as natural antioxidants in meat products: A review. Food Res. Int. 2018, 106, 1095–1104. [Google Scholar] [CrossRef]
  11. Munekata, P.E.S.; Domínguez, R.; Campagnol, P.C.B.; Franco, D.; Trindade, M.A.; Lorenzo, J.M. Effect of natural antioxidants on physicochemical properties and lipid stability of pork liver pâté manufactured with healthy oils during refrigerated storage. J. Food Sci. Technol. 2017, 54, 4324–4334. [Google Scholar] [CrossRef] [PubMed]
  12. Młynarczyk, K.; Walkowiak-Tomczak, D.; Łysiak, G.P. Bioactive properties of Sambucus nigra L. as a functional ingredient for food and pharmaceutical industry. J. Funct. Foods 2018, 40, 377–390. [Google Scholar] [CrossRef]
  13. Milena, V.; Tatjana, M.; Gökhan, Z.; Ivana, B.; Aleksandra, C.; Mohammad, M.F.; Marija, R. Advantages of contemporary extraction techniques for the extraction of bioactive constituents from black elderberry (Sambucus nigra L.) flowers. Ind. Crops Prod. 2019, 136, 93–101. [Google Scholar] [CrossRef]
  14. Integrated Taxonomic Information System. Available online: https://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=35315#null (accessed on 6 October 2021).
  15. Lim, T.K. Edible Medicinal and Non Medicinal Plants, 1st ed.; Springer: Dodrecht, The Netherlands, 2015; p. 1036. ISBN 978-94-017-9510-4. [Google Scholar]
  16. Finn, C.E.; Thomas, A.L.; Byers, P.L.; Serçe, S. Evaluation of American (Sambucus canadensis) and European (S. nigra) elderberry genotypes grown in diverse environments and implications for cultivar development. Hort. Sci. 2008, 43, 1385–1391. [Google Scholar] [CrossRef] [Green Version]
  17. Senica, M.; Stampar, F.; Veberic, R.; Mikulic-Petkovsek, M. Processed elderberry (Sambucus nigra L.) products: A beneficial or harmful food alternative? LWT Food Sci. Technol. 2016, 72, 182–188. [Google Scholar] [CrossRef]
  18. Oniszczuk, A.; Olech, M.; Oniszczuk, T.; Wojtunik-Kulesza, K.; Wójtowicz, A. Extraction methods, LC-ESI-MS/MS analysis of phenolic compounds and antiradical properties of functional food enriched with elderberry flowers or fruits. Arab. J. Chem. 2016, 12, 4719–4730. [Google Scholar] [CrossRef] [Green Version]
  19. Marisa Ribeiro, A.; Estevinho, B.N.; Rocha, F. Microencapsulation of polyphenols—The specific case of the microencapsulation of Sambucus nigra L. extracts—A review. Trends Food Sci. Technol. 2020, 105, 454–467. [Google Scholar] [CrossRef]
  20. Ağalar, H.G. Elderberry (Sambucus nigra L.). In Nonvitamin and Nonmineral Nutritional Supplements, 1st ed.; Seyed, N., Nabavi, A.S., Eds.; Academic Press: Cambridge, MA, USA, 2019; Volume 1, pp. 211–215. [Google Scholar]
  21. Wu, X.; Gu, L.; Prior, R.L.; McKay, S. Characterization of anthocyanins and proanthocyanidins in some cultivars of Ribes, Aronia, and Sambucus and their antioxidant capacity. J. Agric. Food Chem. 2004, 52, 7846–7856. [Google Scholar] [CrossRef] [PubMed]
  22. Vlachojannis, C.; Zimmermann, B.F.; Chrubasik-Hausmann, S. Quantification of anthocyanins in elderberry and chokeberry dietary supplements. Phytother. Res. 2015, 29, 561–565. [Google Scholar] [CrossRef] [PubMed]
  23. Drugs and Lactation Database (LactMed) Bethesda (MD): National Library of Medicine (US). Elderberry; 2006. Available online: https://www.ncbi.nlm.nih.gov/books/NBK501835/ (accessed on 6 October 2021).
  24. Krauze-Baranowska, M.; Malinowska, I.; Głód, D.; Majdan, M.; Wilczańska, A. UTLC of flavonols in Sambucus nigra flowers. J. Planar. Chromat. 2009, 22, 385–387. [Google Scholar] [CrossRef]
  25. Chen, H.; Miao, Q.; Geng, M.; Liu, J.; Hu, Y.; Tian, L.; Pan, J.; Yang, Y. Anti-tumor effect of rutin on human neuroblastoma cell lines through inducing G2/M cell cycle arrest and promoting apoptosis. Sci. World J. 2013, 2013, 269165. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Baldovska, S.; Roychoudhury, S.; Bandik, M.; Mihal, M.; Mnahoncakova, E.; Arvay, J.; Pavlik, A.; Slama, P.; Kolesarova, A. Ovarian steroid hormone secretion by human granulosa cells after supplementation of Sambucus nigra L. extract. Phys. Res. 2021, 70, 755–764. [Google Scholar] [CrossRef] [PubMed]
  27. Stuppner, S.; Mayr, S.; Beganovic, A.; Beć, K.; Grabska, J.; Aufschnaiter, U.; Groeneveld, M.; Rainer, M.; Jakschitz, T.; Bonn, G.K.; et al. Near-Infrared Spectroscopy as a Rapid Screening Method for the Determination of Total Anthocyanin Content in Sambucus Fructus. Sensors 2020, 20, 4983. [Google Scholar] [CrossRef] [PubMed]
  28. Vlachojannis, J.E.; Cameron, M.; Chrubasik, S. A systematic review on the sambuci fructus effect and efficacy profiles. Phytother. Res. 2010, 24, 1–8. [Google Scholar] [CrossRef]
  29. Gleńsk, M.; Gliński, J.A.; Włodarczyk, M.; Stefanowicz, P. Determination of ursolic and oleanolic acid in Sambuci fructus. Chem. Biodivers. 2014, 11, 1939–1944. [Google Scholar] [CrossRef]
  30. Krüger, S.; Mirgos, M.; Morlock, G.E. Effect-directed analysis of fresh and dried elderberry (Sambucus nigra L.) via hyphenated planar chromatography. J. Chromatogr. A 2015, 1426, 209–219. [Google Scholar] [CrossRef] [PubMed]
  31. Salvador, A.C.; Rocha, S.M.; Silvestre, A.J.D. Lipophilic phytochemicals from elderberries (Sambucus nigra L.): Influence of ripening, cultivar and season. Ind. Crop. Prod. 2015, 71, 15–23. [Google Scholar] [CrossRef]
  32. Tejero, J.; Jiménez, P.; Quinto, E.J.; Cordoba-Diaz, D.; Garrosa, M.; Cordoba-Diaz, M.; Gayoso, M.J.; Girbes, T. Elderberries: A source of ribosome-inactivating proteins with lectin activity. Molecules 2015, 20, 2364–2387. [Google Scholar] [CrossRef] [Green Version]
  33. Chowdhury, S.R.; Ray, U.; Chatterjee, B.P.; Roy, S.S. Targeted apoptosis in ovarian cancer cells through mitochondrial dysfunction in response to Sambucus nigra agglutinin. Cell Death Dis. 2017, 8, e2762. [Google Scholar] [CrossRef] [Green Version]
  34. Diviš, P.; Pořízka, J.; Vespalcová, M.; Matějíček, A.; Kaplan, J. Elemental composition of fruits from different black elder (Sambucus nigra L.) cultivars grown in the Czech Republic. J. Elem. 2015, 20, 549–557. [Google Scholar] [CrossRef]
  35. Ho, G.T.; Zou, Y.F.; Wangensteen, H.; Barsett, H. RG-I regions from elderflower pectins substituted on GalA are strong immunomodulators. Int. J. Biol. Macromol. 2016, 92, 731–738. [Google Scholar] [CrossRef]
  36. Ho, G.T.; Kase, E.T.; Wangensteen, H.; Barsett, H. Effect of Phenolic Compounds from Elderflowers on Glucose- and Fatty Acid Uptake in Human Myotubes and HepG2-Cells. Molecules 2017, 22, 90. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Jørgensen, U.; Hansen, M.; Christensen, L.P.; Jensen, K.; Kaack, K. Olfactory and quantitative analysis of aroma compounds in elder flower (Sambucus nigra L.) drink processed from five cultivars. J. Agric. Food Chem. 2000, 48, 2376–2383. [Google Scholar] [CrossRef] [PubMed]
  38. Buhrmester, R.A.; Ebinger1a, J.E.; Seigler, D.S. Sambunigrin and cyanogenic variability in populations of Sambucus canadensis L. (Caprifoliaceae). Biochem. Syst. Ecol. 2000, 28, 689–695. [Google Scholar] [CrossRef]
  39. Ulbricht, C.; Basch, E.; Cheung, L.; Goldberg, H.; Hammerness, P.; Isaac, R.; Khalsa, K.P.S.; Romm, A.; Rychlik, I.; Varghese, M.; et al. An evidence-based systematic review of elderberry and elderflower (Sambucus nigra) by the Natural Standard Research Collaboration. J. Diet. Suppl. 2014, 11, 80–120. [Google Scholar] [CrossRef] [PubMed]
  40. Torabian, G.; Bahramian, B.; Zambon, A.; Spilimbergo, S.; Adil, Q.; Schindeler, A.; Valtchev, P.; Dehghani, F. A hybrid process for increasing the shelf life of elderberry juice. J. Supercrit. Fluids 2018, 140, 406–414. [Google Scholar] [CrossRef]
  41. Porter, R.S.; Bode, R.F. A Review of the Antiviral Properties of Black Elder (Sambucus nigra L.) Products. Phytother. Res. 2017, 31, 533–554. [Google Scholar] [CrossRef]
  42. Frøkiær, H.; Henningsen, L.; Metzdorff, S.B.; Weiss, G.; Roller, M.; Flanagan, J.; Fromentin, E.; Ibarra, A. Astragalus root and elderberry fruit extracts enhance the IFN-β stimulatory effects of Lactobacillus acidophilus in murine-derived dendritic cells. PLoS ONE 2012, 7, e47878. [Google Scholar] [CrossRef]
  43. Waknine-Grinberg, J.H.; El-On, J.; Barak, V.; Barenholz, Y.; Golenser, J. The immunomodulatory effect of Sambucol on leishmanial and malarial infections. Planta Med. 2009, 75, 581–586. [Google Scholar] [CrossRef] [PubMed]
  44. Ho, G.T.; Wangensteen, H.; Barsett, H. Elderberry and Elderflower Extracts, Phenolic Compounds, and Metabolites and Their Effect on Complement, RAW 264.7 Macrophages and Dendritic Cells. Int. J. Mol. Sci. 2017, 18, 584. [Google Scholar] [CrossRef] [Green Version]
  45. Burns, J.J.; Zhao, L.; Taylor, E.W.; Spelman, K. The influence of traditional herbal formulas on cytokine activity. Toxicology 2010, 278, 140–159. [Google Scholar] [CrossRef] [PubMed]
  46. Olejnik, A.; Kowalska, K.; Olkowicz, M.; Rychlik, J.; Juzwa, W.; Myszka, K.; Dembczyński, R.; Białas, W. Anti-inflammatory effects of gastrointestinal digested Sambucus nigra L. fruit extract analyzed in co-cultured intestinal epithelial cells and lipopolysaccharide- stimulated macrophages. J. Funct. Foods 2015, 19, 649–660. [Google Scholar] [CrossRef]
  47. Dawidowicz, A.L.; Wianowska, D.; Baraniak, B. The antioxidant properties of alcoholic extracts from Sambucus nigra L. (antioxidant properties of extracts). LWT Food Sci. Technol. 2006, 39, 308–315. [Google Scholar] [CrossRef]
  48. Denev, P.; Ciz, M.; Ambrozova, G.; Lojek, A.; Yanakieva, I.; Kratchanova, M. Solid-phase extraction of berries’ anthocyanins and evaluation of their antioxidative properties. Food Chem. 2010, 123, 1055–1061. [Google Scholar] [CrossRef]
  49. Sun-Waterhouse, D.; Jin, D.; Waterhouse, G.I.N. Effect of adding elderberry juice concentrate on the quality attributes, polyphenol contents and antioxidant activity of three fibre-enriched pastas. Food Res. Int. 2013, 54, 781–789. [Google Scholar] [CrossRef]
  50. Topolska, D.; Valachova, K.; Rapta, P.; Silhar, S.; Panghyova, E.; Horvath, A.; Soltes, L. Antioxidative properties of Sambucus nigra extracts. Chem. Pap. 2015, 69, 1202–1210. [Google Scholar] [CrossRef]
  51. Arjoon, A.V.; Saylor, C.V.; May, M. In Vitro efficacy of antimicrobial extracts against the atypical ruminant pathogen Mycoplasma mycoides subsp. capri. BMC Complement. Altern. Med. 2012, 12, 169. [Google Scholar] [CrossRef] [Green Version]
  52. Jonušaite, K.; Venskutonis, P.R.; Martínez-Hernández, G.B.; Nieto, G.; López-Gómez, A.; Marín-Iniesta, F. Antioxidant and Antimicrobial Effect of Plant Essential Oils and Sambucus nigra Extract in Salmon Burgers. Foods 2021, 10, 776. [Google Scholar] [CrossRef]
  53. Roschek, B.; Fink, R.C.; McMichael, M.D.; Li, D.; Alberte, R.S. Elderberry flavonoids bind to and prevent H1N1 infection in vitro. Phytochemistry 2009, 70, 1255–1261. [Google Scholar] [CrossRef]
  54. Kinoshita, E.; Hayashi, K.; Katayama, H.; Hayashi, T.; Obata, A. Anti-influenza virus effects of elderberry juice and its fractions. Biosci. Biotechnol. Biochem. 2012, 76, 1633–1638. [Google Scholar] [CrossRef]
  55. Zafra-Stone, S.; Yasmin, T.; Bagchi, M.; Chatterjee, A.; Vinson, J.A.; Bagchi, D. Berry anthocyanins as novel antioxidants in human health and disease prevention. Mol. Nutr. Food Res. 2007, 51, 675–683. [Google Scholar] [CrossRef]
  56. Araújo, K.C.F.; de MBCosta, E.M.; Pazini, F.; Valadares, M.C.; de Oliveira, V. Bioconversion of quercetin and rutin and the cytotoxicity activities of the transformed products. Food Chem. Toxicol. 2013, 51, 93–96. [Google Scholar] [CrossRef]
  57. Schröder, L.; Richter, D.U.; Piechulla, B.; Chrobak, M.; Kuhn, C.; Schulze, S.; Abarzua, S.; Jeschke, U.; Weissenbacher, T. Effects of Phytoestrogen Extracts Isolated from Elder Flower on Hormone Production and Receptor Expression of Trophoblast Tumor Cells JEG-3 and BeWo, as well as MCF7 Breast Cancer Cells. Nutrients 2016, 8, 616. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  58. Pereira, D.I.; Amparo, T.R.; Almeida, T.C.; Costa, F.S.F.; Brandão, G.C.; Santos, O.D.H.D.; da Silva, G.N.; Bianco de Souza, G.H. Cytotoxic activity of butanolic extract from Sambucus nigra L. flowers in natura and vehiculated in micelles in bladder cancer cells and fibroblasts. Nat. Prod. Res. 2020, 1–9. [Google Scholar] [CrossRef] [PubMed]
  59. Ma, X.; Ning, S. Cyanidin-3-glucoside attenuates the angiogenesis of breast cancer via inhibiting STAT3/VEGF pathway. Phytother. Res. 2019, 33, 81–89. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  60. Abdel-Naim, A.B.; Alghamdi, A.A.; Algandaby, M.M.; Al-Abbasi, F.A.; Al-Abd, A.M.; Eid, B.G.; Abdallah, H.M.; El-Halawany, A.M. Rutin Isolated from Chrozophora tinctoria Enhances Bone Cell Proliferation and Ossification Markers. Oxid. Med. Cell Longev. 2018, 2018, 5106469. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  61. Ataee, R.; Falahati, A.; Ebrahimzadeh, M.A.; Shokrzadeh, M. Anticonvulsant activities of Sambucus nigra. Eur. Rev. Med. Pharmacol. Sci. 2016, 20, 3123–3126. [Google Scholar] [PubMed]
  62. Kashi, D.S.; Shabir, A.; Boit, M.D.; Bailey, S.J.; Higgins, M.D. The Efficacy of Administering Fruit-Derived Polyphenols to Improve Health Biomarkers, Exercise Performance and Related Physiological Responses. Nutrients 2019, 11, 2389. [Google Scholar] [CrossRef] [Green Version]
  63. Mahmoudi, M.; Ebrahimzadeh, M.A.; Dooshan, A.; Arimi, A.; Ghasemi, N.; Fathiazad, F. Antidepressant activities of Sambucus ebulus and Sambucus nigra. Eur. Rev. Med. Pharmacol. Sci. 2014, 18, 3350–3353. [Google Scholar]
  64. Blumenthal, M.; Goldberg, A.; Brinckmann, J. Herbal Medicine. Expanded Commission E Monographs; Integrative Medicine Communications: Newton, MA, USA, 2000; ISBN 0967077214. [Google Scholar]
  65. Weiss, R.F.; Fintelmann, V. Herbal Medicine, 2nd ed.; Thieme: New York, NY, USA, 2000; p. 448. ISBN 0865779708. [Google Scholar]
  66. Lin, P.; Hwang, E.; Ngo, H.T.T.; Seo, S.A.; Yi, T.H. Sambucus nigra L. ameliorates UVB-induced photoaging and inflammatory response in human skin keratinocytes. Cytotechnology 2019, 71, 1003–1017. [Google Scholar] [CrossRef]
  67. Chen, C.; Zuckerman, D.M.; Brantley, S.; Sharp, M.; Childress, K.; Hoiczyk, E.; Pendleton, F.A.R. Sambucus nigra extracts inhibit infectious bronchitis virus at an early point during replication. BMC Vet. Res. 2014, 10, 24. [Google Scholar] [CrossRef] [Green Version]
  68. Torabian, G.; Valtchev, P.; Adil, Q.; Dehghani, F. Anti-influenza activity of elderberry (Sambucus nigra). J. Funct. Foods 2019, 54, 353–360. [Google Scholar] [CrossRef]
  69. Harnett, J.; Oakes, K.; Carè, J.; Leach, M.; Brown, D.; Cramer, H.; Pinder, T.A.; Steel, A.; Anheyer, D. The effects of Sambucus nigra berry on acute respiratory viral infections: A rapid review of clinical studies. Adv. Integr. Med. 2020, 7, 240–246. [Google Scholar] [CrossRef] [PubMed]
  70. Badescu, L.; Badulescu, O.; Badescu, M.; Ciocoiu, M. Mechanism by Sambucus nigra Extract Improves Bone Mineral Density in Experimental Diabetes. Evid. Based Complement. Alternat. Med. 2012, 2012, 848269. [Google Scholar] [CrossRef] [Green Version]
  71. Bhattacharya, S.; Christensen, K.B.; Olsen, L.C.; Christensen, L.P.; Grevsen, K.; Færgeman, N.J.; Kristiansen, K.; Young, J.F.; Oksbjerg, N. Bioactive components from flowers of Sambucus nigra L. increase glucose uptake in primary porcine myotube cultures and reduce fat accumulation in Caenorhabditis elegans. J. Agric. Food Chem. 2013, 61, 11033–11040. [Google Scholar] [CrossRef] [PubMed]
  72. Christensen, K.B.; Petersen, R.K.; Kristiansen, K.; Christensen, L.P. Identification of bioactive compounds from flowers of black elder (Sambucus nigra L.) that activate the human peroxisome proliferator-activated receptor (PPAR) gamma. Phytother. Res. 2010, 24, S129–S132. [Google Scholar] [CrossRef] [PubMed]
  73. Gray, A.M.; Abdel-Wahab, Y.H.; Flatt, P.R. The traditional plant treatment, Sambucus nigra (elder), exhibits insulin-like and insulin-releasing actions in vitro. J. Nutr. 2000, 130, 15–20. [Google Scholar] [CrossRef] [PubMed]
  74. Jiang, H.; Zhang, W.; Li, X.; Xu, Y.; Cao, J.; Jiang, W. The anti-obesogenic effects of dietary berry fruits: A review. Food Res. Int. 2021, 147, 110539. [Google Scholar] [CrossRef] [PubMed]
  75. Farrell, N.J.; Norris, G.H.; Ryan, J.; Porter, C.M.; Jiang, C.; Blesso, C.N. Black elderberry extract attenuates inflammation and metabolic dysfunction in diet-induced obese mice. Br. J. Nutr. 2015, 114, 1123–1131. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  76. Duymuş, H.G.; Göger, F.; Başer, K.H.C. In vitro antioxidant properties and anthocyanin compositions of elderberry extracts. Food Chem. 2014, 155, 112–119. [Google Scholar] [CrossRef]
  77. Moldovan, B.; David, L.; Achim, M.; Clichici, S.; Filip, G.A. A green approach to phytomediated synthesis of silver nanoparticles using Sambucus nigra L. fruits extract and their antioxidant activity. J. Mol. Liq. 2016, 221, 271–278. [Google Scholar] [CrossRef]
  78. Silva, P.; Ferreira, S.; Nunes, F.M. Elderberry (Sambucus nigra L.) by-products a source of anthocyanins and antioxidant polyphenols. Ind. Crops Prod. 2017, 95, 227–234. [Google Scholar] [CrossRef]
  79. Iacopini, P.; Baldi, M.; Storchi, P.; Sebastiani, L. Catechin, epicatechin, quercetin, rutin and resveratrol in red grape: Content, in vitro antioxidant activity and interactions. J. Food Compost. Anal. 2008, 21, 589–598. [Google Scholar] [CrossRef]
  80. Bagchi, D.; Sen, C.K.; Bagchi, M.; Atalay, M. Anti-angiogenic, antioxidant, and anti-carcinogenic properties of a novel anthocyanin-rich berry extract formula. Biochemistry 2004, 69, 75–80. [Google Scholar] [CrossRef] [PubMed]
  81. Malagolini, N.; Catera, M.; Osorio, H.; Reis, C.A.; Chiricolo, M.; Dall’Olio, F. Apoptotic cells selectively uptake minor glycoforms of vitronectin from serum. Apoptosis 2013, 18, 373–384. [Google Scholar] [CrossRef]
  82. Chiodelli, P.; Rezzola, S.; Urbinati, C.; Federici Signori, F.; Monti, E.; Ronca, R.; Presta, M.; Rusnati, M. Contribution of vascular endothelial growth factor receptor-2 sialylation to the process of angiogenesis. Oncogene 2017, 36, 6531–6541. [Google Scholar] [CrossRef]
  83. Ho, G.T.T.; Ahmed, A.; Zou, Y.F.; Aslaksen, T.; Wangensteen, H.; Barsett, H. Structure–activity relationship of immunomodulating pectins from elderberries. Carbohydr. Polym. 2015, 125, 314–322. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Barsett, H.; Aslaksen, T.H.; Gildhyal, P.; Michaelsen, T.E.; Paulsen, B.S. Comparison of carbohydrate structures and immunomodulating properties of extracts from berries and flowers of Sambucus nigra L. Eur. J. Med. Plants 2012, 2, 216–229. [Google Scholar] [CrossRef]
  85. Sirotkin, A.V.; Harrath, A.H. Phytoestrogens and their effects. Eur. J. Pharmacol. 2014, 741, 230–236. [Google Scholar] [CrossRef]
  86. Lin, Y.; Jiang, M.; Chen, W.; Zhao, T.; Wei, Y. Cancer and ER stress: Mutual crosstalk between autophagy, oxidative stress and inflammatory response. Biomed. Pharmacother. 2019, 118, 109249. [Google Scholar] [CrossRef]
  87. Wang, Y.; Chen, F.; Ye, L.; Zirkin, B.; Chen, H. Steroidogenesis in Leydig cells: Effects of aging and environmental factors. Reproduction 2017, 154, R111–R122. [Google Scholar] [CrossRef] [Green Version]
  88. Hu, X.Q.; Song, R.; Zhang, L. Effect of Oxidative Stress on the Estrogen-NOS-NO-KCa Channel Pathway in Uteroplacental Dysfunction: Its Implication in Pregnancy Complications. Oxid. Med. Cell Longev. 2019, 2019, 9194269. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  89. Sirotkin, A.V.; Radosová, M.; Tarko, A.; Fabova, Z.; Martín-García, I.; Alonso, F. Abatement of the Stimulatory Effect of Copper Nanoparticles Supported on Titania on Ovarian Cell Functions by Some Plants and Phytochemicals. Nanomaterials 2020, 10, 1859. [Google Scholar] [CrossRef] [PubMed]
  90. Hu, T.; Yuan, X.; Ye, R.; Zhou, H.; Lin, J.; Zhang, C.; Zhang, H.; Wei, G.; Dong, M.; Huang, Y.; et al. Brown adipose tissue activation by rutin ameliorates polycystic ovary syndrome in rat. J. Nutr. Biochem. 2017, 47, 21–28. [Google Scholar] [CrossRef] [PubMed]
  91. Wang, X.; Wang, G.C.; Rong, J.; Wang, S.W.; Ng, T.B.; Zhang, Y.B.; Lee, K.F.; Zheng, L.; Wong, H.K.; Yung, K.K.L.; et al. Identification of Steroidogenic Components Derived from Gardenia jasminoides Ellis Potentially Useful for Treating Postmenopausal Syndrome. Front. Pharmacol. 2018, 9, 390. [Google Scholar] [CrossRef] [PubMed]
  92. Luo, H.; Jiang, B.H.; King, S.M.; Chen, Y.C. Inhibition of cell growth and VEGF expression in ovarian cancer cells by flavonoids. Nutr. Cancer 2008, 60, 800–809. [Google Scholar] [CrossRef] [PubMed]
  93. De Araújo, M.E.; Moreira Franco, Y.E.; Alberto, T.G.; Sobreiro, M.A.; Conrado, M.A.; Priolli, D.G.; Frankland Sawaya, A.C.; Ruiz, A.L.; de Carvalho, J.E.; de Oliveira Carvalho, P. Enzymatic de-glycosylation of rutin improves its antioxidant and antiproliferative activities. Food Chem. 2013, 141, 266–273. [Google Scholar] [CrossRef] [Green Version]
  94. Aqil, F.; Jeyabalan, J.; Agrawal, A.K.; Kyakulaga, A.H.; Munagala, R.; Parker, L.; Gupta, R.C. Exosomal delivery of berry anthocyanidins for the management of ovarian cancer. Food Funct. 2017, 8, 4100–4107. [Google Scholar] [CrossRef]
  95. Diaconeasa, Z.; Leopold, L.; Rugină, D.; Ayvaz, H.; Socaciu, C. Antiproliferative and antioxidant properties of anthocyanin rich extracts from blueberry and blackcurrant juice. Int. J. Mol. Sci. 2015, 16, 2352–2365. [Google Scholar] [CrossRef] [Green Version]
  96. Lim, W.; Jeong, W.; Song, G. Delphinidin suppresses proliferation and migration of human ovarian clear cell carcinoma cells through blocking AKT and ERK1/2 MAPK signaling pathways. Mol. Cell Endocrinol. 2016, 422, 172–181. [Google Scholar] [CrossRef]
  97. Sirotkin, A.; Záhoranska, Z.; Tarko, A.; Popovska-Percinic, F.; Alwasel, S.; Harrath, A.H. Plant isoflavones can prevent adverse effects of benzene on porcine ovarian activity: An in vitro study. Environ. Sci. Pollut. Res. Int. 2020, 27, 29589–29598. [Google Scholar] [CrossRef] [PubMed]
  98. Sirotkin, A.V. Regulators of Ovarian Functions; Nova Publishers: New York, NY, USA, 2014; p. 194. ISBN 978-1-62948-574-4. [Google Scholar]
  99. Schmitt, E.; Stopper, H. Estrogenic activity of naturally occurring anthocyanidins. Nutr. Cancer 2001, 41, 145–149. [Google Scholar] [CrossRef] [PubMed]
  100. Nanashima, N.; Horie, K.; Maeda, H. Phytoestrogenic Activity of Blackcurrant Anthocyanins Is Partially Mediated through Estrogen Receptor Beta. Molecules 2017, 23, 74. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  101. Wu, Y.; Hankinson, S.E.; Smith-Warner, S.A.; Wang, M.; Eliassen, A.H. Flavonoid Intake and Plasma Sex Steroid Hormones, Prolactin, and Sex Hormone-Binding Globulin in Premenopausal Women. Nutrients 2019, 11, 2669. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  102. Li, X.; Guo, J.; Jiang, X.; Sun, J.; Tian, L.; Jiao, R.; Tang, Y.; Bai, W. Cyanidin-3-O-glucoside protects against cadmium-induced dysfunction of sex hormone secretion via the regulation of hypothalamus-pituitary-gonadal axis in male pubertal mice. Food Chem. Toxicol. 2019, 129, 13–21. [Google Scholar] [CrossRef]
  103. Amado, N.G.; Fonseca, B.F.; Cerqueira, D.M.; Reis, A.H.; Simas, A.B.; Kuster, R.M.; Mendes, F.A.; Abreu, J.G. Effects of natural compounds on Xenopus embryogenesis: A potential read out for functional drug discovery targeting Wnt/β-catenin signaling. Curr. Top. Med. Chem. 2012, 12, 2103–2113. [Google Scholar] [CrossRef]
  104. Matsuo, M.; Sasaki, N.; Saga, K.; Kaneko, T. Cytotoxicity of flavonoids toward cultured normal human cells. Biol. Pharm. Bull. 2005, 28, 253–259. [Google Scholar] [CrossRef] [Green Version]
  105. You, J.; Kim, J.; Lim, J.; Lee, E. Anthocyanin stimulates in vitro development of cloned pig embryos by increasing the intracellular glutathione level and inhibiting reactive oxygen species. Theriogenology 2010, 74, 777–785. [Google Scholar] [CrossRef]
  106. Hicks, E.; Mentler, M.; Arena, H.A.; Current, J.Z.; Whitaker, B.D. Cyanidin improves oocyte maturation and the in vitro production of pig embryos. In Vitro Cell Dev. Biol. Anim. 2020, 56, 577–584. [Google Scholar] [CrossRef]
  107. Xie, N.; Geng, N.; Zhou, D.; Xu, Y.; Liu, K.; Liu, Y.; Liu, J. Protective effects of anthocyanin against apoptosis and oxidative stress induced by arsanilic acid in DF-1 cells. Mol. Biol. Rep. 2019, 46, 301–308. [Google Scholar] [CrossRef]
  108. Massimiani, M.; Lacconi, V.; La Civita, F.; Ticconi, C.; Rago, R.; Campagnolo, L. Molecular Signaling Regulating Endometrium-Blastocyst Crosstalk. Int. J. Mol. Sci. 2019, 21, 23. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  109. Valko-Rokytovská, M.; Očenáš, P.; Salayová, A.; Kostecká, Z. Breast Cancer: Targeting of Steroid Hormones in Cancerogenesis and Diagnostics. Int. J. Mol. Sci. 2021, 22, 5878. [Google Scholar] [CrossRef] [PubMed]
  110. Lins, T.L.B.G.; Gouveia, B.B.; Barberino, R.S.; Silva, R.L.S.; Monte, A.P.O.; Pinto, J.G.C.; Campinho, D.S.P.; Palheta, R.C.; Matos, M.H.T. Rutin prevents cisplatin-induced ovarian damage via antioxidant activity and regulation of PTEN and FOXO3a phosphorylation in mouse model. Reprod. Toxicol. 2020, 98, 209–217. [Google Scholar] [CrossRef] [PubMed]
  111. Pieńkowska, N.; Bartosz, G.; Furdak, P.; Sadowska-Bartosz, I. Delphinidin Increases the Sensitivity of Ovarian Cancer Cell Lines to 3-Bromopyruvate. Int. J. Mol. Sci. 2021, 22, 709. [Google Scholar] [CrossRef] [PubMed]
  112. Chen, B.H.; Stephen Inbaraj, B. Nanoemulsion and Nanoliposome Based Strategies for Improving Anthocyanin Stability and Bioavailability. Nutrients 2019, 11, 1052. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Regulators of female reproductive processes—targets of black elderberry (Sambucus nigra L.) and its constituents, rutin, anthocyanins and agglutinins (simplified). Explanations are provided in the text.
Figure 1. Regulators of female reproductive processes—targets of black elderberry (Sambucus nigra L.) and its constituents, rutin, anthocyanins and agglutinins (simplified). Explanations are provided in the text.
Pharmaceuticals 15 00239 g001
Table 1. Physiological and therapeutic actions of elderberry.
Table 1. Physiological and therapeutic actions of elderberry.
Therapeutic ActionsElderberry PreparationExperimental ModelResultsRef.
Antimicrobial activityWater elderberry fruit extract Mycoplasma mycoides subspecies capri strain GM12, Escherichia coli strain DH5α and Bacillus subtilis strain ATCC 6051In vitro growth inhibition of bacterial pathogens [51]
Antiviral activityEthanol elderberry fruit extract
Concentrated elderberry fruit juice
Madin–Darby canine kidney cells (MDCK)Inhibition of Human Influenza A (H1N1) virus[53,54,68]
Concentrated elderberry fruit juiceFemale BALB/c mice infected with influenza A virusSuppression of the viral replication in the bronchoalveolar lavage fluids (BALFs); increase of the human influenza A virus (IFV)-specific neutralizing antibody in the serum; increase of secretory IgA in BALFs and feces[54]
Ethanol elderberry fruit extractVera cellsInhibition of Infectious Bronchitis virus (IBV) by reduction in virus titers[67]
Anti-inflammatory activityEthanol elderberry fruit
Elderflower extract
Lipopolysaccharide (LPS)-activated cells RAW 264.7 and dendritic cells D2SC/IStrong complement fixating activity and inhibitory effect on NO production[44]
Gastrointestinal digested water elderberry fruit extract Co-cultured human intestinal epithelial cells Caco-2 and lipopolysaccharide (LPS)-activated cells RAW 264.7Downregulation the expression of major genes of inflammatory pathway IL-1β, IL-6, TNF-α and COX-2[46]
Ethanol elderberry fruit extractHuman skin keratinocytes HaCaTsProtective effect against UVB-induced skin photoaging and inflammation; suppression of UVB-induced matrix metalloproteinase-1 (MMP-1) expression and inflammatory cytokine secretion; inhibition of mitogen-activated protein kinases/activator protein 1 (MAPK/AP-1) and nuclear factor- κB (NF-κB) signaling pathways[66]
Immuno-modulatory activityElderberry fruit juiceAlveolar carcinoma cells A549Stimulation of human inflammatory cytokines IL-6, IL-8 and TNF production [68]
Water elderberry fruit extractMurine-derived dendritic cellsStimulation of L. acidophilus-induced IL-12 and IFN-β production[42]
Elderberry extract syrup SambucolNormal human monocytesStimulation of the inflammatory cytokines IL-1β, IL-6, IL-8 and TNFα production; causes a shift in the immune response to inflammation-associated Th1 responses [43]
Antioxidant activityWater elderberry fruit extract
Ethanol elderberry fruit extract
Human intestinal epithelial cells Caco-2 and human skin keratinocytes HaCaTsReduction in the intracellular reactive oxygen species (ROS) production[46,66]
Water elderberry fruit extractWeissberger’s biogenic oxidative systemInhibition of oxidative degradation of hyaluronan (HA); ability to scavenge free radicals[50]
Anticancer activityEthanol elderflower extractBreast carcinoma cells MCF7 Protective effect against breast cancer by reduction of cell proliferation; inhibition of estrogen secretion, downregulation of ERα and upregulation of PR [57]
Butanolic elderflower extractBladder carcinoma cells T24 and human fibroblast cells MRC-5Selective cytotoxic activity in cancer cells[58]
Sambucus nigra agglutininEpithelial ovarian adenocarcinoma cells OAW-42, p53 null OC cells SKOV3, normal epithelial ovarian cell line IOSE-364, mouse fibroblast cells NIH3T3 and lung carcinoma cells A549Protective effect against ovarian cancer by induction of apoptosis in cancer cells and cell cycle arrest before G2/M phase; inhibition of cancer progression; mitochondrial dysfunction through increase in ROS generation and cytochrome-c release; shift of cellular respiration toward oxidative phosphorylation[33]
Antidepressant activityMethanol elderberry fruit extractMale Swiss albino miceAntidepressant potential in forced swimming test (FST) and tail suspension tests (TST)[63]
Antidiabetic activityAqueous elderflower extract Mice abdominal musclesIncrease in muscle glucose uptake, glucose oxidation and glycogenesis[73]
Aqueous elderflower extract Rat pancreatic beta-cells BRIN-BD11Stimulation of insulin secretion [73]
Methanol polyphenolic elderberry fruit extractWistar white male rats, streptozotocin (STZ)-induced hyperglycemic ratsReduction in the body fat in diabetic rats; decrease in the lipid peroxidation level in serum[70]
Methanol elderflower extractPrimary porcine myotube culturesModulation of glucose; increase in glucose uptake[71]
Antiosteoporosis activityMethanol polyphenolic elderberry fruit extractWistar white male rats, streptozotocin (STZ)-induced hyperglycemic ratsImprovement of the bone mineral density and osteoporosis status[70]
Anti-obesogenic activityAnthocyanin-rich spray-dried black elderberry extract C57BL/6 male mice,
diet-induced obese mouse model
Decrease in liver weight, serum triglycerides (TAG), inflammatory markers and insulin resistance; reduction of hepatic cholesterol and lipid synthesis[75]
Methanol elderflower extractMouse embryonic fibroblast cells 3T3-L1Activation of the peroxisome proliferator-activated receptor (PPAR) γ; stimulation of insulin-dependent glucose uptake [72]
Methanol elderflower extractPrimary porcine myotube culturesModulation of lipid metabolism; reduction of
fat accumulation
[71]
Aromatase activityEthanol elderberry fruit
Ethanol elderflower extract
Human ovarian granulosa cells HGL5 Stimulatory effect on ovarian steroidogenesis; upregulation of steroid hormone secretion[26]
Ethanol elderflower extractChorion carcinoma cell lines JEG-3 and BeWoInhibition of estradiol secretion and ERα upregulation[57]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Kolesarova, A.; Baldovska, S.; Kohut, L.; Sirotkin, A.V. Black Elder and Its Constituents: Molecular Mechanisms of Action Associated with Female Reproduction. Pharmaceuticals 2022, 15, 239. https://doi.org/10.3390/ph15020239

AMA Style

Kolesarova A, Baldovska S, Kohut L, Sirotkin AV. Black Elder and Its Constituents: Molecular Mechanisms of Action Associated with Female Reproduction. Pharmaceuticals. 2022; 15(2):239. https://doi.org/10.3390/ph15020239

Chicago/Turabian Style

Kolesarova, Adriana, Simona Baldovska, Ladislav Kohut, and Alexander V. Sirotkin. 2022. "Black Elder and Its Constituents: Molecular Mechanisms of Action Associated with Female Reproduction" Pharmaceuticals 15, no. 2: 239. https://doi.org/10.3390/ph15020239

APA Style

Kolesarova, A., Baldovska, S., Kohut, L., & Sirotkin, A. V. (2022). Black Elder and Its Constituents: Molecular Mechanisms of Action Associated with Female Reproduction. Pharmaceuticals, 15(2), 239. https://doi.org/10.3390/ph15020239

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop