Skip Content
You are currently on the new version of our website. Access the old version .
MoleculesMolecules
  • Review
  • Open Access

15 October 2016

An Overview of Plant Phenolic Compounds and Their Importance in Human Nutrition and Management of Type 2 Diabetes

,
,
,
,
,
,
,
,
1
College of Food Science, Sichuan Agricultural University, No. 46, Xinkang Road, Ya’an 625014, Sichuan, China
2
Stockbridge School of Agriculture, University of Massachusetts, Amherst, MA 01003, USA
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
This article belongs to the Special Issue Selected papers from 2nd International Symposium on Phytochemicals in Medicine and Food (2-ISPMF, Fuzhou, 2017)

Abstract

In this paper, the biosynthesis process of phenolic compounds in plants is summarized, which include the shikimate, pentose phosphate and phenylpropanoid pathways. Plant phenolic compounds can act as antioxidants, structural polymers (lignin), attractants (flavonoids and carotenoids), UV screens (flavonoids), signal compounds (salicylic acid and flavonoids) and defense response chemicals (tannins and phytoalexins). From a human physiological standpoint, phenolic compounds are vital in defense responses, such as anti-aging, anti-inflammatory, antioxidant and anti-proliferative activities. Therefore, it is beneficial to eat such plant foods that have a high antioxidant compound content, which will cut down the incidence of certain chronic diseases, for instance diabetes, cancers and cardiovascular diseases, through the management of oxidative stress. Furthermore, berries and other fruits with low-amylase and high-glucosidase inhibitory activities could be regarded as candidate food items in the control of the early stages of hyperglycemia associated with type 2 diabetes.

1. Introduction

Phenolic compounds are secondary metabolites, which are produced in the shikimic acid of plants and pentose phosphate through phenylpropanoid metabolization [1]. They contain benzene rings, with one or more hydroxyl substituents, and range from simple phenolic molecules to highly polymerized compounds [2] (Figure 1). In the synthesis of phenolic compounds, the first procedure is the commitment of glucose to the pentose phosphate pathway (PPP) and transforming glucose-6-phosphate irreversibly to ribulose-5-phosphate. The first committed procedure in the conversion to ribulose-5-phosphate is put into effect by glucose-6-phosphate dehydrogenase (G6PDH). On the one hand, the conversion to ribulose-5-phosphate produces reducing equivalents of nicotinamide adenine dinucleotide phosphate (NADPH) for cellular anabolic reactions. On the other hand, PPP also produces erythrose-4-phosphate along with phosphoenolpyruvate from glycolysis, which is then used through the phenylpropanoid pathway to generate phenolic compounds after being channeled to the shikimic acid pathway to produce phenylalanine [3,4] (Figure 2). Phenolics are the most pronounced secondary metabolites found in plants, and their distribution is shown throughout the entire metabolic process. These phenolic substances, or polyphenols, contain numerous varieties of compounds: simple flavonoids, phenolic acids, complex flavonoids and colored anthocyanins [5] (Figure 1). These phenolic compounds are usually related to defense responses in the plant. However, phenolic metabolites play an important part in other processes, for instance incorporating attractive substances to accelerate pollination, coloring for camouflage and defense against herbivores, as well as antibacterial and antifungal activities [6,7,8].
Figure 1. Common phenolic compounds in plants comprise an aromatic ring, bear one or more hydroxyl substituents and range from simple phenolic molecules to highly polymerized compounds (modified from Velderrain-Rodríguez et al., 2014) [2].
Figure 2. Biosynthesis of phenol compounds in the pentose phosphate, shikimate and phenylpropanoid pathways in plants (modified from Vattem et al., 2005, and Lin et al., 2010) [3,4].
Phenolic compounds, including stress-linked phytochemicals, have been related to favorable impacts, which are caused by the consumption of fruits and vegetables, particularly due to their antioxidant activity [9]. Balasundram et al., (2006) reviewed [10] the antioxidant activity, occurrence and latent uses of phenolic compounds in plants and agri-industrial by-products. Under those reports, fruits, vegetables and beverages are the principle sources of phenolic compounds in the human diet. Plant polyphenols as dietary antioxidants in human health and disease might protect against oxidative damage. As natural antioxidants, phenolic compounds are found abundantly in plant food and beverages, which play vital parts in pabulum and healthcare. Some research have indicated that phenolic compounds are the most affluent in ordinary human diets among the dietary antioxidants. Lately, phenolic compounds have obtained significant interest based on active reports of their conjectural part in holding back a variety of human illnesses [11,12,13]. It is well-known that normally consumed fresh and processed fruits, for instance raspberries, cranberries, apples, grapes, pears and jams, are the major sources of phenolic compounds, and strawberries and their derived products, like juices [3,14]. This review focuses on the present understanding of the potential efficacy of polyphenols on carbohydrate metabolism and glucose homeostasis, which has been commendably studied in vitro, some clinical experiments and animal models [15].

2. Health Benefits of Phenolic Compounds

The chemical constituents extracted from plants, phenolic compounds, can inhibit the absorption of amylase in the treatment of carbohydrate absorption, such as diabetes [16]. There are many fruits and vegetables that contain phenolic compounds, especially, grapes, berries and tomatoes. Phenolic compounds, for instance phenolic acids and flavonoids, could promote health benefits by reducing the risk of metabolic syndrome and the related complications of type 2 diabetes. However, different groups of phenolic compounds have different biological characteristics, and very little is known about the mechanisms by which they could contribute to the prevention of disease; there still is the need for further studies.
Reactive oxygen (ROS) and reactive nitrogen species (RNS) are highly reactive oxidized molecules, which are generated constantly by normal cellular conditions, for instance the activity of the mitochondrial respiratory chain and inflammation, which could lead to damage in other biological molecules, like proteins and DNA [17,18,19]. The antioxidant enzymes include superoxide dismutase (SOD), glutathione peroxidase (GPx) and catalase (CAT), all of them will play a vital role in getting rid of these oxidants and preventing cellular injury (Figure 3).
Figure 3. Reactive oxygen (ROS) and nitrogen (RNS) species are highly reactive oxidized molecules, including superoxide, peroxide, singlet oxygen, hydroxyl radical, NO and OONO, that are constantly produced under normal cellular conditions, such as during homeostasis and impaired functions, which could lead to cellular damage, like ageing, disease and cell death (modified from Shetty et al., 2004.) [20].
Many studies have reported the advantages of phenolic compounds, such as anti-aging, anti-inflammatory, antioxidant and antiproliferative agents. In addition to the adjustment of the above, there are relevant antioxidant enzymes to counter oxidants [21,22]. Polyphenols, especially flavonoids, phenolic acids and tannins, have the important property of inhibiting α-glucosidase and α-amylase, which are key enzymes and responsible for the digestion of dietary carbohydrates to glucose. Dietary plant polyphenols and polyphenol-rich products modulate carbohydrate and lipid metabolism, attenuate hyperglycemia, dyslipidemia and insulin resistance, improve β-cell function, stimulate insulin secretion, improve adipose tissue metabolism and alleviate oxidative stress, stress-sensitive signaling pathways and inflammatory processes. Polyphenolic compounds can also prevent the development of long-term diabetes complications, including cardiovascular disease, neuropathy, nephropathy and retinopathy. There is evidence that the small crimson fruit of Viburnum dilatatum Thunb has strong antioxidant activity, and cyanidin 3-sambubioside (C3S) and 5-caffeoyl quinic acid (5-CQA) are identified as active compounds, which were orally administered to streptozotocin-induced diabetic rats for four weeks repeatedly. Results are presented as shown in Table 1 [23,24]. From this study, both phenolic acids (gallic and and protocatechuic acids) showed concentration-dependent inhibition of α-amylase and α-glucosidase activities in vitro (Figure 4 and Figure 5). Furthermore, phenolic compounds that are found in beverages, vegetables, galenical pears and berries, may facilitate fitness by decreasing the risk of metabolic syndrome and relevant complications of type 2 diabetes [25].
Table 1. Fasted body weight, body weight gain, tissue weight, ratio of tissue-to-body weight and hemoglobin A1 of rats after the experiment for four weeks a [23].
Figure 4. OH radical scavenging ability of gallic and protocatechuic acids.
Figure 5. Fe2+ chelating ability of gallic and protocatechuic acids.
These effects are attributed in general to the potential ability of the phenolic compounds to reduce, counteract or also repair damage resulting from oxidative stress and inflammation associated with these diseases conditions. Experimental findings from the IC50 values for rat intestinal maltase and porcine pancreatic α-amylase showed 334 and 739 μM, respectively, for (−)-3-O-galloylepicatechin and 150 and 401 μM, respectively, for (−)-3-O-galloylcatechin [26] (Table 2). Molecular biological studies have found that EGCG exhibits a strong inhibitory activity on the proteasome (in vitro activity IC50 = 86 nM; in vivo activity IC50 = 18 μM) [27].
Table 2. Enzyme inhibitors from plant origins and their corresponding inhibition of enzymes in starch digestion.
Many studies have associated the increase in the consumption of fruits and vegetables containing high levels of antioxidant compounds with the reduction on the risk of certain chronic diseases, for instance diabetes and cardiovascular diseases [33,34,35]. Some polyphenol-rich foods, for instance grape, grape seed extract, pomegranate juice and cranberry juice, have been reported to play a beneficial part in reducing cardiovascular risk elements in patients with metabolic syndrome and type 2 diabetes. There is a recent study that aimed to test the hypothesis that grapeseed extract (GSE) may improve these markers in high-risk cardiovascular subjects with type 2 diabetes; thirty-two type 2 diabetes mellitus patients in the study, prescribed a diet or oral glucose-lowering agents, received GSE (600 mg/day) or placebo for four weeks in a double-blind randomized crossover trial, and the results indicate that GSE significantly improved markers of inflammation and glycaemia and improved a sole marker of oxidative stress in obese type 2 diabetic subjects at high risk of cardiovascular events over a four-week period, which suggests that it may have a therapeutic role in decreasing cardiovascular risk [36,37]. Berries are considered good sources of phenolic compounds, such as phenolic acids and flavonoids. Phenolic compounds from berry fruits as nutritional interventions could be considered a valuable tool to prevent the development of age-related neurodegenerative diseases by inflammation and decreasing oxidative stress [34].
According to Seeram (2008) [38], there is a wide range of observed biological properties associated with the phenolic compounds present in berry fruits, and they could be correlated to the type of individual phenolics rather than the total phenolic content. However, very little is known about the phenolic acid bioactive forms in vivo and the mechanisms by which they could contribute to the prevention of disease. Additionally, the little research on the biological effects of phenolic acids has ignored the issue of their possible concentrations in circulation after assimilation, such as the possibility of metabolism [39,40]. Hence, there is a need for more in-depth studies into the bioavailability and metabolism of these compounds, since the in vitro antioxidant activity does not reflect the in vivo biological activity. There is also a need to take into consideration the individual to individual variability for metabolism and the absorption of phenolic compounds. Further, it is known that many phenolic compounds are metabolized by the microbiota in the colon, leading to differences in the rate of metabolism and the products formed [41].

4. Health Benefits of Berry Phenolics for Potential Type 2 Diabetes Management

Many foods and herbal extracts have been reported as having active effects on the diabetic patient. People began to use herbs and their active ingredients to prevent the treatment of diabetes and its complications. The change of the diet structure is gradually being applied to the diet [78]. For example, a diet abundant in fruits and vegetables can reduce the risk of type 2 diabetes, illustrating the beneficial effects on type 2 diabetes with different berries, such as strawberries, raspberries, blueberries and black currants. These are the main contents of the part below.
As discussed previously, α-glucosidase and α-amylase are well-known enzymes in the management of hyperglycemia linked to type 2 diabetes [79]. Many foods and herbal extracts have been reported as having a positive effect in diabetic glycemic control using traditional medicine [80]. Polyphenol withdrawn from red wine, ethanol or a combination of both can control the health of streptozotocin-induced diabetic rats [81]. What is more, because of the antioxidant properties, cereal, fruit and vegetable fiber intake is associated with lower risk of ischemic heart disease and death, especially among old people.
In addition, many studies have reported the beneficial effects on hypertension by polyphenol-rich extracts by retarding the development of hypertension and by normalizing blood pressure [82]. In this condition, some foods and herbs could have the potential to treat hypertension, especially for patients with borderline to mild high blood pressure.
Berries are considered good sources of phenolic compounds, such as flavonoids and phenolic acids. Beyond that, berry fruits are commonly consumed fresh and as derived products, such as canned fruits, yogurts, juices and jams. Many studies have reported the benefits of berry consumption against several types of human cancers [38,83] and metabolic syndrome [84].
The polyphenol components of berries inhibit α-glucosidase and α-amylase enzymes, resulting in reduced blood glucose levels after starch-rich meals [85]. McDougall et al., (2008) studied the potential inhibitory activity of strawberries, raspberries, blueberries and black currants on α-glucosidase and α-amylase enzymes [86]. These authors reported that blueberries and black currants had the highest α-glucosidase inhibitory activity, and strawberries and raspberries had the highest α-amylase inhibitory activity. According to Song et al., (2005) [87], reducing risk for type 2 diabetes was associated with high consumption of berries and apples and a diet rich in fruits and vegetables.
High anthocyanin-containing fruit extracts are obtained from currant, blueberry, raspberry and strawberry, and good α-glucosidase inhibition by these extracts was observed [85,86]. However, Cheplick et al., (2007) reported [88] high α-glucosidase inhibitory activity for a yellow raspberry cultivar among black, red and yellow raspberries, suggesting that the α-glucosidase may be influenced more by specific anthocyanins rather than the actual amount of the overall total plant phenolics. α-amylase inhibitory activity in different raspberry cultivars might be due to some specific phenolics [88], since many fruits, including grapes, raspberries and strawberries, are known to contain high levels of soluble tannins, and these fruits have α-amylase inhibitory properties [85,86].
Wilson et al., (2008) suggested [89] that cranberry juice could represent an attractive means for increasing fruit intake and simultaneously affording positive health benefits. Apostolidis et al., (2007) reported [90] that cranberry-enriched cheese had the highest α-amylase and α-glucosidase inhibitory activities among herb, fruit and fungal-enriched cheeses by in vitro studies. Chambers and Camire (2003) [91] evaluated the ingestion of capsules filled with cranberry juice concentrate by adults with type 2 diabetes for 12 weeks. No significant difference in the blood glucose levels was observed. However, these authors suggested that more concentrated products might have benefits since the commercially-available cranberry juice cocktails contain only 27%–31% cranberry juice.
The potential effects on the in vitro inhibition of α-amylase and α-glucosidase enzymes from different Brazilian strawberry cultivars were shown [92]. These authors reported that strawberries had high α-glucosidase and low α-amylase inhibitory activities, suggesting these fruits as good sources for the potential management of hyperglycemia linked to type 2 diabetes as a part of an overall diet. Apostolidis et al., (2006) reported [93] that the combination of cranberry with oregano, which had higher rosmarinic acid content, contributed to the high antioxidant activity and total phenolic content in the extracts, suggesting potential relevance for type 2 diabetes and related hypertension.
The dietary management of hyperglycemia linked to type 2 diabetes through foods that have high α-glucosidase and moderate α-amylase inhibition has been suggested. This is due to the fact that excessive α-amylase inhibition can lead to undigested starch in the colon and consequent stomach distention and discomfort [56]. Hence, berry fruits with low α-amylase and high α-glucosidase inhibitory activities could be considered as good potential candidates as a part of an overall dietary design to manage early stages of hyperglycemia linked to type 2 diabetes.

5. Health Benefits of Other Phenolics for Potential Type 2 Diabetes Management

The following content is about the beneficial effects of some other phenolics that are exacted from pears, pomegranate peel, Phaseolus vulgaris and Cynara scolymus (artichoke) for potential type 2 diabetes management.
Pear (Pyrus spp.) is one of the most popular fruits, consumed as both fresh fruit and fruit products worldwide. Generally speaking, pear peel contains more nutrient components than its pulp. Pear has been reported as a potential source for polyphenols and triterpenes [94]. Meanwhile, polyphenol plant extracts possess potential key enzyme of type 2 diabetes (α-glucosidase and α-amylase), as well as hypertension disease (angiotensin-converting enzyme) [30,95].
Oboh et al., (2012) sought to investigate the inhibitory effect of phenolic extract from avocado (Persea americana) leaves and fruits on some key enzymes linked to type 2 diabetes (α-amylase and α-glucosidase) [95]; and sodium nitroprusside (SNP)-induced lipid peroxidation in rats’ pancreas in vitro. The result showed that the leaves and fruit of avocado inhibit both α-amylase and α-glucosidase activities in a dose-dependent manner. However, the peel had the highest α-amylase inhibitory activity, while the leaf had the highest α-glucosidase inhibitory activity as revealed by their IC50 value [95].
Punica granatum (Pomegranate) is rich in flavonoids, such as flavonols, flavanols and anthocyanins, hydrolysable tannins, such as ellagitannins and gallotannins, condensing tannins, such as proanthocyanidins, and organic and phenolic acids [30]. The efficiency of pomegranate in type 2 DM could be explained by decreasing the lipid peroxidation and oxidative stress through different mechanisms, such as enhancing the antioxidant activity of some enzymes, reducing reactive oxygen species (ROS), inducing metal chelating activity and inhibiting or activating transcriptional factors, such as PPAR-γ and nuclear factor kappa B [96]. Recently, pomegranate wine (2.0 μg/mL) was found to inhibit NF-kappa B activation in cultured vascular-endothelial cells, and studies performed on human acute monocytic leukemia cell line-1 to differentiate into macrophages showed that the traditional anti-diabetic effect of the methanolic extract from pomegranate flowers (PFE) at 500 mg kg−1·day−1 is due to the enhancement of peroxisome proliferator-activated receptor (PPAR)-γ, a transcription factor that plays an important role in carbohydrate metabolism.
According to an experimental study in diabetic rats with non-alcoholic fatty liver disease, the protective effects of polyphenols from pomegranate flowers could be explained by the increase of liver PON1 mRNA and protein expression that enhanced the body antioxidant capacity and reduced immunoreactive insulin to ameliorate the rat hepatic steatosis.
The common bean (Phaseolus vulgaris L.) with a high content of flavonoids, such as flavonols, flavanones, bioflavonoids, flavones, isoflavones, isoflavans, anthocyanins, pterocarpans and coumestans, is one of the most well-known hypoglycemic herbal drugs. Experimental evidence in diabetic animals indicates that Phaseolus vulgaris extracts are effective in reducing lipid accumulation, glycemia, appetite, weight and carbohydrate absorption. Phaseolus vulgaris made serum levels of HDL-cholesterol, plasma insulin, glutathione, vitamin C and the antiatherogenic index in diabetic rats normal. Another study in streptozotocin-induced diabetic rats concluded that cooked common beans (Phaseolus vulgaris L.) can protect against pancreatic beta-cell damage. Various clinical studies proved that Phaseolus vulgaris contains an alpha-amylase inhibitor, which will inhibit or delay digestion or effect carbohydrate absorption [97,98,99].
Anthocyanins are considered as modulators of adipose tissue metabolism. This study shows that anthocyanins have a significant potency for anti-obesity and to ameliorate fat cell dysfunction, as well as the secretion of adipocytokines in insulin resistance, increasing β-oxidation and reducing fat accumulation in adipose cells [100]. Corchorus olitorius leaf extracts are a type of polyphenol (free and bound) with inhibitory activities influencing key enzymes (α-amylase and α-glucosidase) linked to type 2 diabetes and through the inhibitory activities against type 2 diabetes. Inhibition of α-amylase and α-glucosidase activities by these extracts coupled with high antioxidant activity could be part of the mechanism by which C. olitorius leaf exhibits its anti-diabetic properties by preventing hyperglycemia and oxidative stress and damage to biomolecules (lipids, proteins, DNA). In addition, ACE inhibition may explain the antihypertensive properties. These characteristics can be attributed to its phenolic constituents, such as caffeic acid, chlorogenic acid and isorhamnetin, which are abundant in the leaf. However, this is an in vitro finding with possible physiological implications [95].
Cynara scolymus (artichoke) is a perennial herb of the Compositae family, being wide-ranging and considered for its anti-hypercholesterolemic and glucose-lowering effects. An artichoke globe presents no fat, 170 mg of potassium and is rich in vitamin C, cynarin, orthophenole derivates, magnesium, folate and dietary fiber [101]. Recent studies indicated that artichoke flavonoids upregulated nitric-oxide synthase expression in endothelial cells [102]. NO synthesis can be adjusted through the activity of endothelial nitric-oxide synthase (eNOS); the eNOS can generate both nitric oxide (NO), causing blood vessels to dilate, and superoxide, making blood vessels shrink. Therefore, eNOS, having abilities, such as antithrombotic, anti-atherosclerotic and the antihypertensive properties of endothelial NO, is important in regulating vascular function. A study on the endothelial hybrid cell line (EA.hy 926) cells, a cell line derived from human umbilical vein endothelial cells (HUVECs), has found that artichoke leaf extract (ALE), containing large amounts of polyphenolic compounds, can increase eNOS promoter activity in a concentration-dependent manner and, so, influence NO synthesis. That is the way that artichoke flavonoids upregulated nitric-oxide synthase expression to regulate vascular function. Another experimental study in normal and obese rats showed that artichoke extract lowers blood sugar [103]. A clinical study proved that Cynara scolymus supplements are also effective on glucose metabolism in patients with impaired fasting glycemia.
Plant polyphenols can improve the endogenous antioxidative system, effectively prevent oxidative damage and improve oxidant-antioxidant balance. The research on green tea shows that it contains six primary catechins as the polyphenolic compounds that are the most common in this field; and these bioactive components reduced lipid peroxidation and increased plasma total antioxidant capacity. Stress-sensitive signaling pathways, preoxidant enzymes and the induction of antioxidant enzymes, including superoxide dismutase, catalase and glutathione peroxidase, were also decreased [104]. In conclusion, one of the pathogenic mechanisms that describes the increase and progression of micro- and macro-vascular complications in diabetes is oxidative stress; increased production of free radicals and an impaired antioxidant defense system in diabetes induce the state of oxidation/antioxidant imbalance [105]. Inhibition of these oxidative processes could prevent the onset and development of long-term diabetic complications [106].

6. Some Suggestions on Natural Phenolic Compounds and Perspectives

Nowadays, more and more people are beginning to pay attention to gestational diabetes mellitus (GDM). A balanced diet can help prevent and manage several human diseases and metabolic disorders. Examples verify that a higher intake of phenolic compounds and flavonoids from food (vegetables and fruits) is consistently associated with a significantly lower risk of the GDM [107]. In addition, these studies have found positive results for resveratrol on treating diabetes, cardiovascular disease or heart disease [108]. Several lines of evidence also show that high antioxidant content fruits and vegetables may reduce the risk of certain chronic diseases, such as type 2 diabetes, and are associated with the increased risk of microvascular and macrovascular complications. Therefore, phenolic compounds of fruits and vegetables have great potential for the management of type 2 diabetes by controlling hyperglycemia, its macrovascular complications, such as hypertension, and microvascular complications linked to cellular oxidative breakdown. There is usually a large number of different substances and a distribution of conjugated forms of phenolic compounds along with functionality among berry fruits that could be taken advantage of for planning compatible functional advantages for the management of the metabolic syndrome of the chronic disease state. Especially, berry fruits could be determined as a part of a general healthy diet for the management of postprandial hyperglycemia, due to their ability to inhibit α-glucosidase simultaneously with low inhibition of α-amylase, which probably lead to less adverse effects. Further, the similar profiles of bioactive phenolic compounds also have potential, which avoid cellular oxidative breakdown linked to macro- and micro-vascular complications, as well as hypertension, respectively. Natural plant phenolic compounds present in a wide variety of natural plants have played an effective role in the treatment of type 2 diabetes, so it will be a major research direction that should be explored in today’s society.
Type 2 diabetes is a polygenic metabolic disease characterized by a concomitant impairment of the metabolic functions of several organs. The anti-diabetic effects of phenolic phytochemicals are similar due to the integration of several complementary mechanisms. It is a difficult task to elucidate the mode of actions of these polyphenolic compounds given their large numbers and the specific regulation of their bioavailability as determined by their absorption and biotransformation. Due to the in vitro inhibitory effects of plant-based food extracts (grape seed, green tea and white tea) and their constituent flavan-3-ol monomers (catechins) on α-amylase and α-glucosidase activity, two key glucosidases required for starch digestion in humans [109], the potential role of natural phenolic compounds is discussed.
Type 2 diabetes is a cluster of metabolic disorders. And type 2 diabetes is associated with other pathogenic conditions, including subclinical inflammation and oxidative stress. The pathogenic conditions result in long-term diabetes complications and insulin resistance. The escalating tendency in the prevalence rate of diabetes complications hints that recent medical treatments for the management of diabetes are not adequate, and the use of additional treatments, which consist of their nutraceuticals and functional foods, could raise the validity of diabetes management. Polyphenols in plants, which include phenolic acids, lignans, stilbenes and flavonoids, based on in vitro research, clinical trials and some animal models, have been proposed as efficient supplements for diabetes management and as preventive of its long-term complications. Further investigations making use of human clinical research are required to affirm the useful results of polyphenolic compounds as additional treatments for diabetic patients.

7. Conclusions

Summing up from the context, high levels of antioxidant compounds and a diet abundant in fruits and vegetables could potentially reduce the risk of type 2 diabetes and the associated increased risk of microvascular and macrovascular complications. Therefore, within the context phenolic antioxidants, those available from berries have excellent potential for managing type 2 diabetes through the control of hyperglycemia and its macrovascular complications, such as hypertension and microvascular complications linked to cellular oxidative breakdown. High phenolic antioxidant activity suggests that certain phenolic compounds are present in select species, which could prove to be beneficial towards human health if included as part of food designs for a healthy diet. This review provides a biochemical rationale for clinical studies on the functional benefits of fruits and vegetables, which could further be applied in in vivo studies for the development and innovation of therapeutic strategies, to prevent and manage type 2 diabetes.

Acknowledgments

The authors thank the “211 Engineering Double Support Plan”, Sichuan Agricultural University and the Education Department of Sichuan Province major project for financial support.

Author Contributions

Derong Lin initiated the writing of this review and designed the structure of this review, interpreted results, and drafted the manuscript. Mengshi Xiao, Jingjing Zhao and Zhuohao Li compiled information and made contribution to the revision of the manuscript. Baoshan Xing designed the structure of this review, interpreted results, and revised the language. Xindan Li, Maozhu Kong and Liangyu Li gave some valuable advices about the structure of the manuscript and the upcoming research issues of natural phenolic compounds. Qing Zhang, Yaowen Liu and Hong Chen compiled information and made contribution to the revision of the manuscript. Wen Qin, Hejun Wu and Saiyan Chen made certain contribution to the language modification of the review.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Randhir, R.; Lin, Y.T.; Shetty, K. Stimulation of phenolics, antioxidant and antimicrobial activities in dark germinated mung bean sprouts in response to peptide and phytochemical elicitors. Process Biochem. 2004, 39, 637–646. [Google Scholar] [CrossRef]
  2. Velderrain-Rodríguez, G.R.; Palafox-Carlos, H.; Wall-Medrano, A.; AyalaZavala, J.F.; Chen, C.-Y.O.; Robles-Sanchez, M.; Astiazaran-García, H.; Alvarez-Parrilla, E.; González-Aguilar, G.A. Phenolic compounds: Their journey after intake. Food Funct. 2014, 5, 189–197. [Google Scholar] [CrossRef] [PubMed]
  3. Vattem, D.A.; Randhir, R.; Shetty, K. Cranberry phenolics-mediated antioxidant enzyme response in oxidatively stressed porcine muscle. Process. Biochem. 2005, 40, 2225–2238. [Google Scholar] [CrossRef]
  4. Lin, D.R.; Hu, L.J.; You, H.; Sarkar, D.; Xing, B.S.; Shetty, K. Initial screening studies on potential of high phenolic-linked plantclonal systems for nitrate removal in cold latitudes. J. Soils Sediment. 2010, 10, 923–932. [Google Scholar] [CrossRef]
  5. Babbar, N.; Oberoi, H.S.; Sandhu, S.K.; Bhargav, V.K. Influence of different solvents in extraction of phenolic compounds from vegetable residues and their evaluation as natural sources of antioxidants. J. Food Sci. Technol. 2014, 51, 2568–2575. [Google Scholar] [CrossRef] [PubMed]
  6. Alasalvar, C.; Grigor, J.M.; Zhang, D.L.; Quantick, P.C.; Shahidi, F. Comparison of volatiles, phenolics, sugars, antioxidant vitamins, and sensory quality of different colored carrot varieties. J. Agric. Food Chem. 2001, 49, 1410–1416. [Google Scholar] [CrossRef] [PubMed]
  7. Acamovic, T.; Brooker, J.D. Biochemistry of plant secondary metabolites and their effects in animals. Proc. Nutr Soc. 2005, 64, 403–412. [Google Scholar] [CrossRef] [PubMed]
  8. Edreva, A.; Velikova, V.; Tsonev, T.; Dagnon, S.; Gürel, A.L.; Aktas, L. Stress-protective role of secondary metabolites: Diversity of functionsand mechanisms. Gen. Appl. Plant. Physiol. 2008, 34, 67–78. [Google Scholar]
  9. Heima, K.E.; Tagliaferroa, A.R.; Bobilya, D.J. Flavonoid antioxidants: Chemistry, metabolism and structure-activity relationships. J. Nutr. Biochem. 2002, 13, 572–584. [Google Scholar] [CrossRef]
  10. Balasundram, N.; Sundram, K.; Samman, S. Phenolic compounds in plants and agri-industrial by-products: Antioxidant activity, occurrence, and potential uses. Food Chem. 2006, 99, 191–203. [Google Scholar] [CrossRef]
  11. Fiorentino, A.; D’Abrosca, B.; Pacifico, S.; Mastellone, C.; Piccolella, S.; Monaco, P. Isolation and structure elucidation of antioxidant polyphenols from quince (Cydonia vulgaris) peels. J. Agric. Food Chem. 2008, 56, 2660–2667. [Google Scholar] [CrossRef] [PubMed]
  12. Hoper, L.; Cassidy, A. A review of the health care potential of bioactive compounds. J. Sci. Food Agric. 2006, 86, 1805–1813. [Google Scholar] [CrossRef]
  13. Pu, F.; Ren, X.L.; Zhang, X.P. Phenolic compounds and antioxidant activity in fruits of six Diospyros kaki genotypes. Eur. Food Res. Technol. 2013, 237, 923–932. [Google Scholar] [CrossRef]
  14. Pinto, M.S.; Lajolo, F.M.; Genovese, M.I. Bioactive compounds and antioxidant capacity of strawberry jams. Plant. Foods Hum. Nutr. 2007, 62, 127–131. [Google Scholar] [CrossRef] [PubMed]
  15. Hanhineva, K.; Törrönen, R.; Bondia-Pons, I.; Pekkinen, J.; Kolehmainen, M.; Mykkänen, H.; Poutanen, H. Impact of dietary polyphenols on carbohydrate metabolism. Int. J. Mol. Sci. 2010, 11, 1365–1402. [Google Scholar] [CrossRef] [PubMed]
  16. Sales, P.M.; Souza, P.M.; Simeoni, L.A.; Magalhães, P.O.; Silveira, D. α-Amylase Inhibitors: A Review of Raw Material and Isolated Compounds from Plant Source. J. Pharm. Pharm. Sci. 2012, 15, 141–183. [Google Scholar] [CrossRef] [PubMed]
  17. Halliwell, B. Effect of diet on cancer development: Is oxidative DNA damage a biomarker. Free Radic. Biol. Med. 2002, 32, 968–974. [Google Scholar] [CrossRef]
  18. Urso, M.L.; Clarkson, P.M. Oxidative stress, exercise, and antioxidant supplementation. Toxicology 2003, 189, 41–54. [Google Scholar] [CrossRef]
  19. Lea, A.J.; Tung, J.; Zhou, X. A Flexible, Efficient Binomial Mixed Model for Identifying Differential DNA Methylation in Bisulfite Sequencing Data. PLoS Genet. 2015, 11, e1005650. [Google Scholar] [CrossRef] [PubMed]
  20. Shetty, K.; Wahlqvist, M.L. A model for the role of the proline-linked pentose-phosphate pathway in phenolic phytochemical bio-synthesis and mechanism of action for human health and environmental applications. Asia Pac. J. Clin. Nutr. 2004, 13, 1–24. [Google Scholar] [PubMed]
  21. Shukitt-Hale, B.; Lau, F.C.; Joseph, J.A. Berry fruit supplementation and the aging brain. J. Agric. Food Chem. 2008, 56, 636–641. [Google Scholar] [CrossRef] [PubMed]
  22. Moo-Huchin, V.M.; Moo-Huchin, M.I.; Estrada-León, R.J.; Cuevas-Gloryc, L.; Estrada-Motaa, I.A.; Ortiz-Vázquezc, E.; Betancur-Anconad, D.; Sauri-Duchc, E. Antioxidant compounds, antioxidant activity and phenolic content in peel from three tropical fruits from Yucatan, Mexico. Food Chem. 2015, 166, 17–22. [Google Scholar] [CrossRef] [PubMed]
  23. Iwai, K.; Kim, M.Y.; Onodera, A.; Matsue, H. Alpha-glucosidase inhibitory and antihyperglycemic effects of polyphenols in the fruit of Viburnum dilatatum Thunb. J. Agric. Food Chem. 2006, 54, 4588–4592. [Google Scholar] [CrossRef] [PubMed]
  24. Iwai, K. Antidiabetic and antioxidant effects of polyphenols in brown alga Ecklonia stolonifera in genetically diabetic KK-A(y) mice. Plant Foods Hum. Nutr. 2008, 63, 163–169. [Google Scholar] [CrossRef] [PubMed]
  25. Dembinska-Kiec, A.; Mykkänen, O.; Kiec-Wilk, B.; Mykkänen, H. Antioxidant phytochemicals against type 2 diabetes. Br. J. Nutr. 2008, 99, 109–117. [Google Scholar] [CrossRef] [PubMed]
  26. Bhandari, M.R.; Jong-Anurakkun, N.; Hong, G.; Kawabata, J. α-Glucosidase and α-amylase inhibitory activities of Nepalese medicinal herb Pakhanbhed (Bergenia. ciliata, Haw.). Food Chem. 2008, 106, 247–252. [Google Scholar] [CrossRef]
  27. Dongkui, S. Design, Synthesis and Preliminary Activity Evaluationg of Catechins Proteasome Inhibitors. Master Thesis, Ocean University of China, Qingdao, China, 1 June 2009. [Google Scholar]
  28. Kawakami, K.; Aketa, S.; Nakanami, M. Major water-soluble polyphenols, proanthocyanidins, in leaves of persimmon (Diospyros kaki) and their α-amylase inhibitory activity. Biosci. Biotechnol. Biochem. 2010, 74, 1380–1385. [Google Scholar] [CrossRef] [PubMed]
  29. Shobana, S.; Sreerama, Y.N.; Malleshi, N.G. Composition and enzyme inhibitory properties of finger millet (Eleusine coracana L.) seed coat phenolics: Mode of inhibition of α-glucosidase and pancreatic amylase. Food Chem. 2009, 115, 1268–1273. [Google Scholar] [CrossRef]
  30. Zhang, X.Z.; Sathitsuksanoh, N.; Zhu, Z.G. One-step production of lactate from cellulose as the sole carbon source without any other organic nutrient by recombinant cellulolytic Bacillus subtilis. Metab. Eng. 2011, 13, 364–372. [Google Scholar] [CrossRef] [PubMed]
  31. Gao, H.; Huang, Y.N.; Xu, P.Y.; Kawabata, J. Inhibitory effect on α-glucosidase by the fruits of terminalia chebula retz. Food Chem. 2007, 105, 628–634. [Google Scholar] [CrossRef]
  32. Ani, V.; Akhilender, Naidu K. Antihyperglycemic activity of polyphenolic components of black/bitter cumin Centratherum anthelminticum (L.) Kuntze seeds. Eur. Food Res. Technol. 2008, 4, 897–903. [Google Scholar] [CrossRef]
  33. Costacou, T.; Mayer-Davis, E.J. Nutrition and prevention of type 2 diabetes. Ann. Rev. Nutr. 2003, 23, 147–170. [Google Scholar] [CrossRef] [PubMed]
  34. Hung, H.C.; Joshipura, K.J.; Jiang, R. Fruit and vegetable intake and risk of major chronic disease. J. Natl. Cancer Inst. 2004, 96, 1577–1584. [Google Scholar] [CrossRef] [PubMed]
  35. Nöthlings, U.; Schulze, M.B.; Weikert, C. Intake of vegetables, legumes, and fruit, and risk for all-cause, cardiovascular, and cancer mortality in a European diabetic population. J. Nutr. 2008, 138, 775–781. [Google Scholar] [PubMed]
  36. Kar, P.; Laight, D.; Rooprai, H.K.; Shaw, K.M.; Cummings, M. Effects of grape seed extract in Type 2 diabetic subjects at high cardiovascular risk: A double blind randomized placebo controlled trial examining metabolic markers, vascular tone, inflammation, oxidative stress and insulin sensitivity. Diabet. Med. 2009, 26, 526–531. [Google Scholar] [CrossRef] [PubMed]
  37. Shidfar, F.; Heydari, I.; Hajimiresmaiel, S.J. The effects of cranberry juice on serum glucose, apoB, apoA-I, Lp(a), and Paraoxonase-1 activity in type 2 diabetic male patients. J. Res. Med. Sci. 2012, 17, 355–360. [Google Scholar] [PubMed]
  38. Seeram, N.P. Berry fruits for cancer prevention: Current status and future prospects. J. Agri. Food Chem. 2008, 56, 630–635. [Google Scholar] [CrossRef] [PubMed]
  39. Rechner, A.R.; Kuhnle, G.; Bremner, P.; Hubbard, G.P.; Moore, K.P.; Rice-Evans, C.A. The metabolic fate of dietary polyphenols in humans. Free Radic. Biol. Med. 2002, 33, 220–235. [Google Scholar] [CrossRef]
  40. Helenoa, S.A.; Martins, A.; Queiroz, M.J.R.P.; Ferreira, I.C.F.R. Bioactivity of phenolic acids: Metabolites versus parent compounds: A review. Food Chem. 2015, 173, 501–513. [Google Scholar] [CrossRef] [PubMed]
  41. Espín, J.C.; García-Conesa, M.T.; Tomás-Barberán, F.A. Nutraceuticals: Facts and fiction. Phytochemistry 2007, 68, 2986–3008. [Google Scholar] [CrossRef] [PubMed]
  42. Lindström, J.; Absetz, P.; Hemiö, K.; Peltomäki, P.; Peltonen, M. Reducing the risk of type 2 diabetes with nutrition and physical activity-efficacy and implementation of lifestyle interventions in Finland. Public Health Nutr. 2010, 13, 993–999. [Google Scholar] [CrossRef] [PubMed]
  43. Shaw, J.E.; Sicree, R.A.; Zimmet, P.Z. Global estimates of the prevalence of diabetes for 2010 and 2030. Diabetes Res. Clin. Pract. 2010, 87, 4–14. [Google Scholar] [CrossRef] [PubMed]
  44. Alhazmi, A.; Stojanovski, E.; McEvoy, M.; Brownand, W.; Garg, M.L. Diet quality score is a predictor of type 2 diabetes risk in women: The Australian Longitudinal Study on Women’s Health. Br. J. Nutr. 2014, 112, 945–951. [Google Scholar] [CrossRef] [PubMed]
  45. Whitmore, C. Type 2 diabetes and obesity in adults. Br. J. Nutr. 2010, 19, 882–886. [Google Scholar] [CrossRef] [PubMed]
  46. DeFronzo, R.A.; Bonadonna, R.C.; Ferrannini, E. Pathogenesis of NIDDM: Abalanced overview. Diabetes Care 1992, 15, 318–368. [Google Scholar] [CrossRef] [PubMed]
  47. Pickup, J.C. Inflammation and activated innate immunity in the pathogenesis of type 2 diabetres. Diabetes Care 2004, 27, 813–823. [Google Scholar] [CrossRef] [PubMed]
  48. Smith, M.A.; Taneda, S.; Richey, P.L.; Miyata, S.; Yan, S.D.; Stern, D. Advanced Maillard reaction end products are associated with Alzheimer disease pathology. Proc. Natl. Acad. Sci. USA 1994, 91, 5710–5714. [Google Scholar] [CrossRef] [PubMed]
  49. Winer, N.; Sowers, J.R. Epidemiology of diabetes. J. Clin. Pharmacol. 2004, 44, 397–405. [Google Scholar] [CrossRef] [PubMed]
  50. García-Alonso, J.; Ros, G.; Vidal-Guevara, M.L.; Periago, M.J. Acute intake of phenolic-rich juice improves antioxidant status in healthy subjects. Nutr. Res. 2006, 26, 330–339. [Google Scholar] [CrossRef]
  51. Kajimoto, Y.; Kaneto, H. Role of oxidative stress in pancreatic beta-cell dysfunction. Ann. NY Acad. Sci. 2004, 1011, 168–176. [Google Scholar]
  52. Drews, G.; Krippeit-Drews, P.; Düfer, M. Oxidative stress and beta-cell dysfunction. Pflug. Arch. Eur. J. Phy. 2010, 460, 703–718. [Google Scholar] [CrossRef] [PubMed]
  53. Szkudelski, T.; Szkudelska, K. Anti-diabetic effects of resveratrol. Ann. NY Acad. Sci. 2011, 1215, 34–39. [Google Scholar] [CrossRef] [PubMed]
  54. Yin, P.; Zhao, S.; Chen, S. Hypoglycemic and hypolipidemic effects of polyphenols from burs of Castanea mollissima Blume. Molecules 2011, 16, 9764–9774. [Google Scholar] [CrossRef] [PubMed]
  55. Ford, E.S.; Giles, W.H.; Mokdad, A.H. Increasing Prevalence of the Metabolic Syndrome Among U.S. Adults. Diabetes Care 2004, 27, 2444–2449. [Google Scholar] [CrossRef] [PubMed]
  56. Cai, L.M.; Shi, Y.C. Self-assembly of short linear chains to α- and β-type starch spherulites and their enzymatic digestibility. J. Agric. Food Chem. 2013, 61, 10787–10797. [Google Scholar] [CrossRef] [PubMed]
  57. Mccue, P.; Shetty, K. Inhibitory effects of rosmarinic acid extracts on porcine pancreatic amylase in vitro. Asia Pac. J. Clin. Nutr. 2004, 13, 101–106. [Google Scholar] [PubMed]
  58. Johnston, K.; Sharp, P.; Clifford, M.; Morgan, L. Dietary polyphenols decrease glucose uptake by human intestinal Caco-2 cells. FEBS Lett. 2005, 579, 1653–1657. [Google Scholar] [CrossRef] [PubMed]
  59. Dao, T.M.; Waget, A.; Klopp, P. Resveratrol increases glucose induced GLP-1 secretion in mice: A mechanism which contributes to the glycemic control. PLoS ONE 2011, 6, 0020700. [Google Scholar] [CrossRef] [PubMed]
  60. Kotowaroo, M.I.; Mahomoodally, M.F.; Gurib-Fakim, A.; Subratty, A.H. Screening of traditional antidiabetic medicinal plants of Mauritius for possible α-amylase inhibitory effects in vitro. Phytother. Res. 2006, 20, 228–231. [Google Scholar] [CrossRef] [PubMed]
  61. Prabhakar, P.K.; Doble, M. Synergistic effect of phytochemicals in combination with hypoglycemic drugs on glucose uptake in myotubes. Phytomedicine 2009, 16, 1119–1126. [Google Scholar] [CrossRef] [PubMed]
  62. Kumar, R.; Balaji, S.; Uma, T.S.; Sehgal, P.K. Fruit extracts of Momordica charantia potentiate glucose uptake and up-regulate Glut-4, PPAR gamma and PI3K. J. Ethnopharmacol. 2009, 126, 533–537. [Google Scholar] [CrossRef] [PubMed]
  63. Ford, E.S.; Mokdad, A.H. Fruit and vegetable consumption and diabetes mellitus incidence among U.S. Adults. Prev. Med. 2001, 32, 33–39. [Google Scholar] [CrossRef] [PubMed]
  64. Fogli-Cawley, J.J.; Dwyer, J.T.; Saltzman, E. The 2005 Dietary Guidelines for Americans and risk of the metabolic syndrome. Am. J. Clin. Nutr. 2007, 86, 1193–1201. [Google Scholar] [PubMed]
  65. McCarty, M.F. Nutraceutical resources for diabetes prevention-an update. Med. Hypoth. 2005, 64, 151–158. [Google Scholar] [CrossRef] [PubMed]
  66. Greenberg, J.A.; Boozer, C.N.; Geliebter, A. Coffee, diabetes, and weight control. Am. J. Clin. Nutr. 2006, 84, 682–693. [Google Scholar] [PubMed]
  67. Kobayashi, Y.; Suzuki, M.; Satsu, H. Green tea polyphenols inhibit the sodium-dependent glucose transporter of intestinal epithelial cells by a competitive mechanism. J. Agric. Food Chem. 2000, 48, 5618–5623. [Google Scholar] [CrossRef] [PubMed]
  68. Bassoli, B.K.; Cassolla, P.; Borba-Murad, G.R. Chlorogenic acid reduces the plasma glucose peak in the oral glucose tolerance test: Effects on hepatic glucose release and glycaemia. Cell. Biochem. Funct. 2008, 26, 320–328. [Google Scholar] [CrossRef] [PubMed]
  69. Mostaedi, R.; Lackey, D.E.; Adams, S.H.; Dada, S.A.; Hoda, Z.A.; Ali, M.R. Prevalence of undiagnosed and inadequately treated type 2 diabetes mellitus, and dyslipidemia in morbidly obese patients who present for bariatric surgery. Obes. Surg. 2014, 24, 927–935. [Google Scholar] [CrossRef] [PubMed]
  70. Heart Outcomes Prevention Evaluation (HOPE) Study Investigators. Effects of ramipril on cardiovascular and microvascular outcomes in people with diabetes mellitus: Rresults of the HOPE study and MICRO-HOPE substudy. Heart Outcomes Prevention Evaluation Study Investigators. Lancet 2000, 355, 253–259. [Google Scholar]
  71. Suzuki, A.; Kagawa, D.; Fujii, A.; Ochiai, R.; Tokimitsu, I.; Saitob, I. Short and long-term effects of ferulic acid on blood pressure in spontaneously hypertensive rats. Am. J. Hypert. 2002, 15, 351–357. [Google Scholar] [CrossRef]
  72. Suzuki, A.; Fujii, A.; Jokura, H.; Tokimitsu, I.; Hase, T.; Saito, I. Hydroxyhydroquinone interferes with the chlorogenic acid-induced restoration of endothelial function in spontaneously hypertensive rats. Am. J. Hypert. 2008, 21, 23–27. [Google Scholar] [CrossRef] [PubMed]
  73. Kozuma, K.; Tsuchiya, S.; Kohori, J.; Hase, T.; Tokimitsu, I. Antihypertensive effect of green coffee bean extract on mildly hypertensive subjects. Hypert. Res. 2005, 28, 711–718. [Google Scholar] [CrossRef] [PubMed]
  74. Edwards, R.L.; Lyon, T.; Litwin, S.E. Quercetin reduces blood pressure in hypertensive subjects. J. Nutr. 2007, 137, 2405–2411. [Google Scholar] [PubMed]
  75. Nakamura, Y.; Matsumoto, H.; Todoki, K. Endothelium-dependent vaso relaxation induced by black currant concentrate in rat thoracic aorta. Jpn. J. Pharmacol. 2002, 89, 29–35. [Google Scholar] [CrossRef] [PubMed]
  76. Reshefa, N.; Hayarib, Y.; Gorenb, C.; Boaz, M.; Madar, Z.; Knobler, H. Antihypertensive effect of sweetie fruit in patients with stage I hypertension. Am. J. Hypert. 2005, 18, 1360–1363. [Google Scholar] [CrossRef] [PubMed]
  77. Nettleton, J.A.; Harnack, L.J.; Scrafford, C.G.; Mink, P.J.; Barraj, L.M.; Jacobs, D.R., Jr. Dietary flavonoids and flavonoid-rich foods are not associated with risk of type 2 diabetes in postmenopausal women. J. Nutr. 2006, 136, 3039–3045. [Google Scholar] [PubMed]
  78. Arulselvan, P.; Ghofar, H.A.A.; Karthivashan, G.; Halim, M.F.A.; Ghafar, M.S.A.; Fakurazi, S. Antidiabetic therapeutics from natural source: A systematic review. Biomed. Prev. Nutr. 2014, 4, 607–617. [Google Scholar] [CrossRef]
  79. Thilagam, E.; Parimaladevi, B.; Kumarappan, C.; Mandal, S.C. α-Glucosidase and α-amylase inhibitory activity of senna surattensis. J. Acupunct. Meridian Stud. 2013, 6, 24–30. [Google Scholar] [CrossRef] [PubMed]
  80. Yeh, G.Y.; Eisenberg, D.M.; Kaptchuk, T.J.; Phillips, R.S. Systematic review of herbs and dietary supplements for glycemic control in diabetes. Diabetes Care 2003, 26, 1277–1294. [Google Scholar] [CrossRef] [PubMed]
  81. Al-Awwadi, N.; Azay, J.; Poucheret, P. Antidiabetic activity of red wine polyphenolic extract, ethanol or both in streptozotocin-treated rats. J. Agric. Food Chem. 2004, 52, 1008–1016. [Google Scholar] [CrossRef] [PubMed]
  82. Negishi, H.; Xu, J.W.; Ikeda, K.; Njelekela, M.; Nara, Y.; Yamori, Y. Black and green tea polyphenols attenuate blood pressure increases in stroke-prone spontaneously hypertensive rats. J. Nutr. 2004, 134, 38–42. [Google Scholar] [PubMed]
  83. Juranić, Z.; Žižak, Ž. Biological activities of berries: From antioxidant capacity to anti-cancer effects. Biofactors 2005, 23, 207–211. [Google Scholar] [CrossRef] [PubMed]
  84. Tsuda, T. Regulation of adipocyte function by anthocyanins: Possibility of preventing the metabolic syndrome. J. Agric. Food Chem. 2008, 56, 642–646. [Google Scholar] [CrossRef] [PubMed]
  85. McDougall, G.J.; Shpiro, F.; Doboson, P.; Smith, P.; Blake, A.; Stewart, D. Different polyphenolic compounds of soft fruits inhibit α-amylase and α-glucosidase. J. Agric. Food Chem. 2005, 53, 2760–2766. [Google Scholar] [CrossRef] [PubMed]
  86. McDougall, G.J.; Kulkarni, N.N.; Stewart, D. Current developments on the inhibitory activity effects of berry polyphenols on digestive enzymes. BioFactors 2008, 34, 73–80. [Google Scholar] [CrossRef] [PubMed]
  87. Song, Y.Q.; Manson, J.E.; Buring, J.E.; Sesso, H.D.; Liu, S. Associations of dietary flavonoids with risk of type 2 diabetes, and markers of insulin resistance and systemic inflammation in women: A prospective study and crosssectional analysis. J. Am. Coll. Nutr. 2005, 24, 376–384. [Google Scholar] [CrossRef] [PubMed]
  88. Cheplick, S.; Kwon, Y.; Bhowmik, P.; Shetty, K. Clonal variation in raspberry fruit phenolics and relevance for diabetes and hypertension management. J. Food Biochem. 2007, 31, 656–679. [Google Scholar] [CrossRef]
  89. Wilson, T.; Singh, A.P.; Vorsa, N. Human Glycemic Response and Phenolic Content of Unsweetened Cranberry Juice. J. Med. Food. 2008, 11, 46–54. [Google Scholar] [CrossRef] [PubMed]
  90. Apostolidis, E.; Kwon, Y.I.; Shetty, K. Inhibitory potential of herb, fruit, and fungal-enriched cheese against key enzymes linked to type 2 diabetes and hypertension. Inn. Food Sci. Emerg. Technol. 2007, 8, 46–54. [Google Scholar] [CrossRef]
  91. Chambers, B.K.; Camire, M.E. Can cranberry supplementation benefit adults with type 2 diabetes. Diabetes Care 2003, 26, 2695–2696. [Google Scholar] [CrossRef] [PubMed]
  92. Pinto, M.S.; Lajolo, F.M.; Genovese, M.I. Bioactive compounds and quantification of total ellagic acid in strawberries (Fragaria. X ananassa Duch.). Food Chem. 2008, 107, 1629–1635. [Google Scholar] [CrossRef]
  93. Apostolidis, E.; Kwon, Y.I.; Shetty, K. Potential of cranberry-based herbal synergies for diabetes and hypertension management. Asia Pac. J. Clin. Nutr. 2006, 15, 433–441. [Google Scholar] [PubMed]
  94. Li, X.; Wang, T.; Zhou, B.; Gao, W.Y.; Cao, J.G.G.; Huangc, L.Q. Chemical composition and antioxidant and anti-inflammatory potential of peels and flesh from 10 different pear varieties (Pyrus spp.). Food Chem. 2014, 152, 531–538. [Google Scholar] [CrossRef] [PubMed]
  95. Oboh, G.; Ademiluyi, A.O.; Akinyemi, A.J.; Henle, T.; Saliua, J.A.; Schwarzenbolz, U. Inhibitory effect of polyphenol-rich extracts of jute leaf (Corchorus olitorius) on key enzyme linked to type 2 diabetes(a-amylase and a-glucosidase) and hypertension (angiotensin I converting) in vitro. J. Funct. Foods 2012, 4, 450–458. [Google Scholar] [CrossRef]
  96. Banihani, S.; Swedan, S.; Alguraan, Z. Pomegranate and type 2 diabetes. Nutr. Res. 2013, 33, 341–348. [Google Scholar] [CrossRef] [PubMed]
  97. Pari, L.; Venkateswaran, S. Effect of an aqueous extract of Phaseolus vulgaris on plasma insulin and hepatic key enzymes of glucose metabolism in experimental diabetes. Die Pharm. 2003, 58, 916–919. [Google Scholar]
  98. Pari, L.; Venkateswaran, S. Protective role of Phaseolus vulgaris on changes in the fatty acid composition in experimental diabetes. J. Med. Food 2004, 7, 204–209. [Google Scholar] [CrossRef] [PubMed]
  99. Dragan, S.; Andrica, F.; Serban, M.C.; Timar, R. Polyphenols-rich natural products for treatment of diabetes. Curr. Med. Chem. 2015, 22, 14–22. [Google Scholar] [CrossRef] [PubMed]
  100. Tsuda, T.; Horio, F.; Uchida, K.; Hiromitsu, A.; Osawa, T. Dietary cyanidin 3-O-beta-d-glucoside-rich purple corn color prevents obesity and ameliorates hyperglycemia in mice. J. Nutr. 2003, 133, 2125–2130. [Google Scholar] [PubMed]
  101. Trojan-Rodrigues, M.; Alves, T.L.; Soares, G.L.G.; Ritter, M.R. Plants used as antidiabetics in popular medicine in Rio Grande do Sul, southern Brazil. J. Ethnopharmacol. 2012, 139, 155–163. [Google Scholar] [CrossRef] [PubMed]
  102. Li, H.; Xia, N.; Brausch, I.; Yao, Y.; Förstermann, U. Flavonoids from artichoke (Cynara scolymus L.) up-regulate endothelial-type nitric-oxide synthase gene expression in human endothelial cells. J. Pharmacol. Exp. Ther. 2004, 310, 926–932. [Google Scholar] [CrossRef] [PubMed]
  103. Fantini, N.; Colombo, G.; Giori, A. Evidence of glycemia-lowering effect by a Cynara scolymus L. extract in normal and obese rats. Phytother. Res. 2011, 25, 463–466. [Google Scholar] [CrossRef] [PubMed]
  104. Crespy, V.; Williamson, G. A review of the health effects of green tea catechins in in vivo animal models. J. Nutr. 2004, 134, 3431–3440. [Google Scholar]
  105. Goycheva, P.; Gadjeva, V.; Popov, B. Oxidative stress and its complications in diabetes mellitus. Trakia J. Sci. 2006, 4, 1–8. [Google Scholar]
  106. Pérez-Matute, P.; Zulet, M.A.; Martínez, J.A. Reactive species and diabetes: Counteracting oxidative stress to improve health. Curr. Opin. Pharmacol. 2009, 9, 771–779. [Google Scholar] [CrossRef] [PubMed]
  107. Santangelo, C.; Zicari, A.; Mandosi, E.; Scazzocchio, B.; Mari, E.; Morano, S. Could gestational diabetes mellitus be managed through dietary bioactive compounds? Current knowledge and future perspectives. Br. J. Nutr. 2016, 115, 1129–1144. [Google Scholar] [CrossRef] [PubMed]
  108. Diaz-Gerevini, G.T.; Repossi, G.; Dain, A.; Tarres, M.C.; Das, U.N.; Eynard, A.R. Beneficial action of resveratrol: How and why? Nutrition 2016, 32, 174–178. [Google Scholar] [CrossRef] [PubMed]
  109. Yilmazer-Musa, M.; Griffith, A.M.; Michels, A.J.; Schneider, E.; Frei, B. Grape Seed and Tea Extracts and Catechin 3-Gallates Are Potent Inhibitors of α-Amylase and α-Glucosidase Activity. J. Agric. Food Chem. 2012, 60, 8924–8929. [Google Scholar] [CrossRef] [PubMed]

Article Metrics

Citations

Article Access Statistics

Multiple requests from the same IP address are counted as one view.