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Dietary Polyphenols—Important Non-Nutrients in the Prevention of Chronic Noncommunicable Diseases. A Systematic Review

Wojciech Koch

Nutrients · 2019 · Systematic review · CC BY

doi:10.3390/nu11051039

Abstract

The improvement of the social and economic conditions of society has eliminated the threat of death from the majority of infectious diseases. However, the rapid progress of civilization has created new possibilities for the appearance of factors with adverse effects for the health of society. This has led to increased morbidity from certain diseases, the presence of which had not been observed several centuries ago. Chronic noncommunicable diseases (e.g., cancers, cardio-vascular disorders, diabetes, obesity, neurodegenerative diseases) result from an inappropriate relationship between people and their environment. The common characteristic for all chronic diseases is a “new” form of inflammation, very often called metaflammation, which is considered as a subclinical, permanent inflammation. As a result, metabolic cascade, including cellular oxidative stress, atherosclerotic process, and insulin resistance, occurs, which slowly generates significant deterioration in the organism. Polyphenols are the major group of non-nutrients, considering their diversity, food occurrence, and biological properties. The current review aims to present a wide spectrum of literature data, including the molecular mechanism of their activity and experimental model used, and summarize the recent findings on the multitude of physiological effects of dietary polyphenols towards the prevention of several chronic diseases. However, despite several studies, the estimation of their dietary intake is troublesome and inconclusive, which will be also discussed.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 24, 2026. Paragraph numbers are ours, so an answer can point at one.

Highlights

During recent decades; a significant increase in chronic noncommunicable diseases has been observed; Polyphenols are the main group of biologically active non-nutrients present in food; Estimation of dietary intake of polyphenols is difficult; Beneficial effects of phenolics towards the prevention of lifestyle diseases are reviewed

1. Introduction

The rapid progress of humanity observed starting from the Industrial Revolution and especially after World War II has led to an increase in the length and quality of life. Rapid development of medical and pharmaceutical sciences has led to an improvement in diagnosis and the introduction of new drugs (e.g., vaccination or antibiotics). Together with the improvement of the social and economic conditions of society, this has eliminated the threat of death from the majority of infectious diseases. However, the rapid progress of civilization has created new possibilities for the appearance of factors with adverse effects for the health of society. The Western diet, with its high saturated fat and sugar intake, physical inactivity, insufficient sleep, strong psychological stress, low sun exposure, environmental pollution, and smoking or alcohol abuse, are some of the most important factors which have been discussed during the last 20 years in numerous papers and reports, leading to the description of the many so-called “diseases of civilization”.

2. Chronic Noncommunicable Diseases

Lifestyle diseases are classified as diseases resulting from an inappropriate relationship between people and their environment and lifestyle. They are often described as chronic noncommunicable diseases (NCDs) and are, in general, treated as the same group of diseases. The list of impairments of such a type is increasing. Recently, Egger and Dixon classified chronic diseases with lifestyle or environmental determinants into ten categories: cardio- and cerebrovascular diseasescancers with lifestyle componentsendocrine/metabolic disordersgastrointestinal disorderskidney diseasemental/central nervous system (CNS) healthmusculoskeletal disordersrespiratory diseasesreproductive disordersdermatological disorders

cardio- and cerebrovascular diseases

cancers with lifestyle components

endocrine/metabolic disorders

gastrointestinal disorders

kidney disease

mental/central nervous system (CNS) health

musculoskeletal disorders

respiratory diseases

reproductive disorders

dermatological disorders

2.1. Historical Background

On the basis of anthropological and medical reports, several authors suggest that these diseases are not observed or are rare in hunter-gatherer or nonwesternized populations. This hypothesis is supported by historical records of explorers and adventurers which support the evidence of the superior health of pre-agriculture traditional populations. Deterioration of diet did not start in the last 50 or 100 years; rather, it started much earlier. The Agricultural Revolution started about 11,000 years ago in the Middle East and quickly spread around the globe. “Industrial” food production significantly altered the human diet and lifestyle, which was associated with the introduction of cereal grains as staple foods, domesticated meats, nonhuman milk, legumes, and other cultivated plant foods and later a common use of sucrose and alcoholic drinks. According to Carrera-Bastos et al., the superior physical health and body composition of hunter-gatherers and other traditional populations minimally affected by modern diet and lifestyle were not primarily due to genetics, but to environmental factors. They also suggest that during the last several thousand years, no significant gene changes have occurred to protect humans from chronic diseases caused by modern habits. Based on the anatomical, biomechanical, and isotope analysis of the hominin skeletons, several typical diet and lifestyle characteristics of the hunter-gatherers and traditional populations may be observed; these are presented in Table 1.

The 20th century brought an improvement in sanitation, hygiene, and immunization and the development of antibiotics, which resulted in the overcoming of “germ diseases”. In the 1970s and 1980s in the developed countries of North America, Europe, and the Asian-Pacific region, the process of the “epidemiological transition” started, when chronic diseases began to be more frequent compared to infectious. Currently, this can be observed in developing countries such as Brazil, China, Russia, or India. According to Egger and Dixon, the progress of civilization tamed infectious diseases, but surprisingly instigated an unhealthy style of life, which resulted in the rapid outbreak of NCDs.

2.2. Current Findings on NCDs

The background of NCDs is rather complicated, in contrast to infectious diseases which are always connected with germs. The common characteristic for all chronic diseases is a “new” form of inflammation, which from the beginning of the 1990s has been called metaflammation. This term is used to describe a form of low-grade, chronic, and systemic inflammation, originally associated with obesity. Recent findings have revealed that “metaflammation” is not limited to obesity, but also related to other lifestyle diseases and conditions, for example heart disease, type 2 diabetes, many forms of cancer, osteoporosis, and even central nervous system diseases (depression or dementia). Metaflammation is considered a part of a metabolic cascade, including cellular oxidative stress, atherosclerotic process, and insulin resistance. As a result, dysmetabolism, induced allostatic overload, and finally chronic impairment can be observed. Factors which induce metaflammation have largely arisen since the industrial revolution and have been named “anthropogens” or man-made environmental inducers.

Anthropogens induce low, subclinical, but persistent immune-response to a nonlife-threating situation. This situation could become dysmetabolic if exposure starts to be prolonged. Moreover, low-grade chronic inflammation is often associated with man-made environmental inducers; for example, chronic psychological stress, improper diet, environmental pollution, smoking, and drug and alcohol abuse. Numerous studies have been performed indicating different factors regarding the progress of low-grade chronic inflammation and finally its contribution to NCDs. The most important are insufficient sleep (fewer than 6 h per 24-h day), chronic vitamin D deficiency, physical inactivity, and broadly understood nutritional changes. Surprisingly, these are in contrast to the factors presented in Table 1, which were characteristic for hunter-gatherers and other traditional populations.

2.3. Nutritional Changes Associated with NCDs—Potential Role of Antioxidants

The important role of nutrition for the prevention of chronic diseases is already well known. Inadequate as well as overnutrition may lead to serious consequences. Recent statistics have shown that improper nutrition accounts for up to two-thirds of the risk for type 2 diabetes, cardiovascular diseases (CVD), and other chronic impairments. The diets of industrialized societies are significantly changed compared to Paleolithic or even Ancient Egyptian or Medieval populations. Chronic disease progress has been associated with important nutritional aberrations which have occurred during last few centuries, regarding specific nutrient intake, overall meal patterns, food processing, and general food product characteristics, including glycemic index and macro- and micronutrient density. Numerous studies have indicated dietary risk factors associated with the increased risk of developing noncommunicable diseases:excessive energy intake from high energy-dense/low nutrient-dense productscommon consumption of products with high glycemic load and indexlow dietary fiber intake (in particular, in soluble form)low dietary poly-unsaturated fatty acid (PUFA) intakelow dietary omega-3 fatty acid intakehigh dietary trans fatty acid intakehigh dietary sodium intake and improper sodium/potassium statuslow intake of fruits and vegetableshyperhomocysteinemia associated mostly with a high animal-protein diet

excessive energy intake from high energy-dense/low nutrient-dense products

common consumption of products with high glycemic load and index

low dietary fiber intake (in particular, in soluble form)

low dietary poly-unsaturated fatty acid (PUFA) intake

low dietary omega-3 fatty acid intake

high dietary trans fatty acid intake

high dietary sodium intake and improper sodium/potassium status

low intake of fruits and vegetables

hyperhomocysteinemia associated mostly with a high animal-protein diet

During the last two decades, it has been proposed that oxidative stress, caused by reactive oxygen species (ROS), may be a key factor in the development of insulin resistance, diabetes, cardiovascular diseases, neurodegenerative disorders, and other NCDs. Prolonged exposure of β-cells to oxidative agents (e.g., H2O2) results in their dysfunction and induced insulin resistance and that the use of antioxidants improves insulin sensitivity, which has been proved in in vitro and animal model studies. The role of ROS in the initiation, progression, and clinical consequences of cardiovascular diseases is already well known and has been described in several research papers proposing different mechanisms of antioxidant action in the prevention of CVD.

Although changes in lifestyle and diet (according to the characteristics presented above) are still considered crucial, many authors suggest that increased dietary intake of antioxidants is one of the most important factors in the prevention of NCDs, especially when those antioxidants are taken with a normal diet and not via dietary supplements. The human diet contains many different antioxidants, including vitamins (C, E, β-carotene), trace elements (copper, iron, zinc, selenium), or plant metabolites (polyphenols, carotenoids). Although phytochemicals are often considered antinutrients or non-nutrients, during the last 15 years several findings have shed new light on their positive impact on the human organism, including their significant role in the prevention of chronic diseases. Plant foods contain a wide spectrum of secondary metabolites among which polyphenols are one of the most abundant and nutritionally important phytochemicals. There are over 8000 phenolic structures currently known and over 500 are present in plant foods and are considered dietary polyphenols. Polyphenols are synthetized from the combination of derivates formed from phenylalanine and acetic acid in two biochemical pathways—the shikimate and the acetate pathways. This is a very wide and complex group of phytochemicals, for which the common feature is the presence in their structure of at least one or more phenolic groups, which are responsible for the strong reducing properties of polyphenols. In nature, they occur as simple molecules, for example phenolic acids or flavonoids, or as very complicated polymerized macromolecules with molecular weights of greater than 30,000 Da, such as tannins. The diversity of polyphenols is increased, as they appear in the form of glycosides with one or two sugars, of which glucose is the most abundant molecule. Other sugar residues involve galactose, rhamnose, arabinose, xylose or glucuronic and galacturonic acids, and many others. Direct connections between sugar residues and aromatic carbon atoms (C–C binding) are also common.

3. Polyphenols—Estimation of Daily Dietary Intake Problems

Major classes of polyphenols involve simple phenols, phenolic acids, acetophenones, phenylacetic acids, coumarins, anthraquinones, xanthones, stilbenes, lignans, and flavonoids. The latter are the most complicated and the most widely distributed in plants. Flavonoids account for approximately two-thirds of dietary polyphenols and the remaining one-third are phenolic acids, being the second most important group of phenolics present in foods. Flavonoids are an integral part of animal and human diets and plants are their only sources, as they cannot be synthesized by animals. The most frequent class of flavonoids found in foods are flavonols, which are predominant in fruits in the form of different glycosides. In vegetables, the quercetin derivates are the most abundant flavonoid. Exact estimation of daily dietary intake of flavonoids is difficult given their complicated distribution in plants, variety of classes, techniques used (analytical or calculating methods), and food habits. Moreover, several factors that influence their level in plants (germination, degree of ripeness, light), different flavonoid structures which still have not been identified and food processing cannot be ignored. Another question is whether the study quantify glucoside forms, aglycones, or both. There are plenty of data on phenolic content in plants and assessments of dietary intake found in literature. However, these values mostly do not represent the total intake of all polyphenols, even not all flavonoids. In 1976, Kühnau estimated daily dietary intake of polyphenols at 1 g. Later, those values were very often questioned as being almost impossible to attain from natural sources. Studies from the 1990s suggested that daily dietary intake is much lower, e.g., (values in mg/day):Denmark—26Finland—0–41Greece—15Japan—60–68The Netherlands—33United States—20

Denmark—26

Finland—0–41

Greece—15

Japan—60–68

The Netherlands—33

United States—20

However, those values mostly referred to only three flavonols and two flavones and therefore were underestimated. Later findings shed new light on polyphenolic intake, including flavonoids. A recent study performed by Pozzo and coworkers on 1658 Italian individuals, aged 45–64 years, revealed a mean intake of flavonoids at 320 mg/person/day, with a median of 251 mg/person/day. Food consumption data were based on the semiquantitative food-frequency questionnaire used in the EPIC (European Prospective Investigation into Cancer and Nutrition) and the flavonoid intake was calculated using the latest food composition tables published by the US Department of Agriculture (USDA) and extended by European data. The database contained information on the food content of seven major classes of flavonoids. Flavonoid intake was calculated by multiplying the specific flavonoid content in food servings (expressed as mg aglycone equivalent/100 g food) by the daily consumption of the selected food item (g/day). The study revealed that the main consumed classes of flavonoids were proanthocyanidins and flavan-3-ols with median intakes of 96.1 and 50.4, respectively. The major consumed substances were, among others, polymers of flavon-3-ols, simple and condensed catechins (theaflavins, thearubigins), hesperetin, myricetin, or quercetin. The major sources of flavonoids were fruits, red wine, vegetables, and tea.

Recent studies on polyphenols intake found in the literature are based on calculations using US or European databases, among which the Phenol-Explorer database is one of the most important and widely used. It contains information on the content of 502 polyphenol glycosides, esters, and aglycones in 452 foods and may be helpful in the estimation of daily dietary intake of phenolics. However, values based on estimations using databases are inaccurate, as the content of flavonoids and other polyphenols may vary significantly according to place, harvest time or food processing. Therefore, these values are only approximate and may differ significantly from analytical data, which are hard to collect considering the multitude and structure diversity of dietary polyphenols.

A study performed in Poland on 648 students was based on analytical determinations of selected flavonoids and phenolic acids in reconstructed daily food rations using the HPLC method. Moreover, total phenolic content (TPC) was determined using the Folin–Ciocalteu method. The mean intake of phenolics over the 3-year study period was determined to be 245.8 and 172.7 mg/day in women and men, respectively. The major polyphenol, in both the food rations of women and men, was hesperidin, while quercetin was also consumed in significant amounts—32.6 mg/day among women and 35.8 mg/day among men. The study was limited to the intake of seven phenolic compounds; however, TPC values expressed as gallic acid equivalents were much higher and close to 1 g/day.

According to Pérez-Jiménez and coworkers and based on the Phenol-Explorer database, cloves and dried peppermint are the foodstuffs richest in polyphenols, with content of 15 and 12 g/100 g. Later, food products such as star anise, cocoa powder, Mexican oregano (dried), or celery seed were classified, with contents between 2 and 5 g/100 g. However, the consumption of these products is so low that they cannot be considered important dietary sources of polyphenols. The Phenol-Explorer database suggests that products rich in phenolics, where the intake may be considered significant (amounts and frequency of consumption), contain between 1756 mg (black chokeberry) to 45 mg/100 g (broccoli) of polyphenols. Although black (102 mg/100 g) and green tea (89 mg/100 g) infusions were classified 52 and 54, respectively, according to the classification of the 100 foods with the highest polyphenol content, recently they have been considered the most important sources of dietary polyphenols. The multitude of methods used to evaluate dietary intake of polyphenols caused significant differences between particular results. Figure 1 gathers the most important methods used to estimate the intake of dietary phenolics.

4. Dietary Polyphenols—Natural Substances Beneficial in the Prevention and Treatment of Lifestyle Diseases

A wide spectrum of biological activity of polyphenols has previously been extensively described in numerous scientific papers, including in vitro and in vivo studies. We can see from Figure 2. These natural components of human diet are probably the most extensively described in the scientific literature. Some of their properties may be used in the prevention and treatment of lifestyle diseases. One of the targets of the present review was to gathered some of the interesting and recent findings on the biological properties of selected dietary polyphenols, including molecular mechanism of action, regarding their potential role in reducing the incidence of civilization diseases. Since scientific literature is filled with hundreds of studies focused on biological properties of polyphenols, only research on compounds which dietary intake is significant were considered and described.

4.1. Antioxidant Activities of Dietary Polyphenols

This is probably the most extensively and the most frequently described biological activity of phenolics, which because of their structure, may be related to almost all compounds from this group. Experimental studies revealed that the mechanism of action may include several different pathways: direct ROS scavenging; inhibition of enzymes or trace elements chelation, which are involved in free radicals generation (e.g., copper or iron); increase in endogenic antioxidant production (e.g., SOD (SuperOxide Dismutase), glutathione). Flavonoids are known for their properties to inhibit enzymes which are involved in ROS generation, like glutathione S-transferase, microsomal monooxygenase, mitochondrial succinoxidase or NADH oxidase. Protective role, against free radicals, for other antioxidants (e.g., vitamin C and E) was also proved. In vitro experiments showed that quercetin, epicatechin, and rutin are described by strong antioxidant properties. Quercetin possess strong iron-chelating and iron-stabilizing properties. Epicatechin and rutin were proved to be strong ROS scavengers and inhibitors of lipid peroxidation. Moreover, it was shown that glycosidic forms of polyphenols are usually weaker antioxidants than the corresponding aglycones. Green tea polyphenols were confirmed to significantly increase the antioxidant capacity of human blood serum. Clinical study performed on ten healthy Korean subjects (aged 23–25), which consume 150 mL of green tea infusion in the first week, 300 mL in the second, and 450 mL in the third, showed increased total capacity of serum and plasma. The highest changed was observed after drinking of 300 and 450 mL, whereas after ingestion of 150 mL, no significant differences were observed. Moreover, this study elucidated that the highest increase was observed 120 min after tea consumption.

Not only simple polyphenols derived from tea, but also the products of their condensation, synthesized during the production of fermented and semifermented teas, possess strong antioxidant properties. Theaflavins, which are one of the most important phenolic constituents present in black tea, were proved to be stronger antioxidants in comparison to EGCG (-epigallocatechin-3-gallate), which is considered one of the most active antiradical molecules present in food. Randomized, double-blind, crossover study performed by Arent and co-investigators revealed that consumption of black tea, enriched in theaflavins, led to better recovery and decreased the oxidative stress in humans subjected to acute anaerobic interval training. It was also observed that theaflavins reduced muscle pain after training in comparison to control group. Imran and coworkers studied the influence of theaflavins and thearubigins, which are a dominant fraction of polymeric polyphenols present in black tea, on antioxidant status and lipid peroxidation in rats. They have proved that theaflavins showed higher antioxidant activity compared to thearubigins. A diet rich in both TFs and TRs (thearubigins) showed significant reduction in lipid profile, glucose content, and renal function. Animals receiving TFs were characterized by lower values in the TBARS (thiobarbituric acid reactive substances) test, compared to thearubigins or a mixture of TFs and TRs (1:1). However, theaflavins+thearubigins diets caused the highest glucose, urea, and creatinine reduction and maximum level of insulin and antioxidant parameters compared to diets containing TFs or TRs alone. Another clinical study showed beneficial effects of oolong tea drinking, which is considered the richest source of another condensed compounds of phenolic nature—theasinensins. Research performed on athletes showed that consumption of oolong tea for 30 days caused significant antioxidant effect observed as strong reduction of malondialdehyde at rest and after exercise, decreased levels of SOD at the rest. It was also observed that oolong tea drinking significantly reduced lipid peroxidation and normalized the cholesterol profiles. Among all thesinensins isomers, theasinensin A was considered as the strongest antioxidant agent against lipid peroxidation.

4.2. Anti-Inflammatory Effect

Since low-grade, chronic inflammation is a key factor in the development and progression of lifestyle diseases beneficial effects of polyphenols towards inhibition and reduction of any form of inflammation may be crucial in prevention and treatment of this type of disorders. Several studies revealed positive role of tea polyphenols considering inhibition of different mechanisms of inflammation. EGCG was proved to reduce autoimmune response by affecting the differentiation of the dysregulated CD 4(+) T cells to potential autoimmune agents. Animals experiments proved beneficial effects of EGCG treatment towards the improvement of autoimmune diseases. It was also shown that EGCG inhibits proliferation of autoreactive T cells, production of proinflammatory cytokines and Th1 and Th 17 subpopulations, and increases the amount of regulatory T cells populations in lymphoid tissues and the central nervous system. All these findings suggest that EGCG may have preventive and therapeutic potential regarding T-cell mediated autoimmune diseases. Epigallocatechin-3-gallate was also shown to reduce inflammation in connective tissue. EGCG was injected intraperitoneally 3 times/week into mice with collagen-induced arthritis. Significant reduction in cytokines, phosphorylated-signal transducer and activator of transcription-3, 705 and 727 and oxidative stress proteins production was observed. Moreover, the inhibition of osteoclast and Th 17 production was proved associated with increased regulatory T cells production. As a result, significant reduction in arthritis symptoms has been observed. Not only tea catechins, but also other dietary flavonoids were recently described to have immune-response modulation properties. The recruitment of neutrophils to the site of injury or damage is an early sign of inflammation. Significant reduction of NO (nitric oxide), MPO (myeloperoxidase), and TNF-α (inflammatory mediators) production in human peripheral blood neutrophils by rutin, quercetin, and vitexin in the concentration of 25 µM was observed. These result suggests that dietary flavonoids may have a potential role in treating patients with neutrophil-mediated inflammatory diseases. Apigenin administrated orally significantly reduced the infiltration of the inflammatory cells in the experimental autoimmune myocardiatitis in mice. The production of proinfalammatory cytokines—Th1 cytokines, TNF-α, interferon-gamma (IFN-γ), and interleukin-2 (IL-2) was also limited.

4.3. Anticancer Activity

One of the diseases most frequently associated with improper changes in lifestyle, including dietary habits, are different forms of cancer. Among the biological properties of dietary polyphenols, the cancer-chemopreventive properties in various in vitro and animal models have been extensively reported. This activity may originate from their antioxidant and anti-inflammatory properties. Recently, one of the most frequently investigated phenolics towards potential cancer prevention and treatment are simple and condensed tea polyphenols. Zhang and coworkers revealed induction of apoptosis of hepatocellular carcinoma LM6 cells (HCCLM6), associated with the reduction of mitochondrial membrane potential and promotion of G0/G1 phase cell cycle arrest caused by EGCG. The induced apoptosis of HCCLM6 cells was connected with a significant decrease in Bcl-2 and NF-κB expression. No influence on noncancerous liver cells was proved (HL-7702). Anticancer activity of epigallocatechin-3-galltae was also proved in animal model. Chemopreventive effect of EGCG and TF (theaflavin) in the treatment of tongue and liver cancer induced by N-nitrosodiethylamine in mice was shown. The mechanism of action was associated with the modulation of cellular proliferation/apoptosis and prevalence of CD 44 positive regulation. Significant chemopreventive activity of theaflavins towards prostate cancer was also proved. Two independent studies showed reduction of proliferation and apoptosis induction in human prostate carcinoma (LNaCP and PC-3 cells). Theaflavin caused tumor cell death by induction of p53 suppressor expression and inhibition of nuclear transcription factor NF-κβ and mitogen-activated MAPK-kinase, which are important carcinogenesis factors. The cell cycle blocking in the phase G2/M was also observed. Theaflavins are considered as a promising chemopreventive agent in human prostate cancer as their relative bioavailability in prostate tissue was 70% higher in comparison to EGCG. Other dietary flavonoids are also considered as strong, natural anticancer agents. Recently, numerous studies indicated interesting findings on anticancer properties of the most abundant polyphenolic aglycones in the human diet—quercetin, apigenin, and hesperidin. Recently, quercetin was shown to inhibit of the human retinoblastoma (RB Y79 cell line) growth. Inhibition of tumor progression and invasion in the dose dependent manner was proved. The strongest effect was revealed at the quercetin concentration of 100 µM. Additionally antiangiogenesis effect was also reported. Another recent study performed by Hashemzaei and co-investigators showed significant anticancer activity in in vitro and in vivo models. Quercetin used at the concentrations of 10, 20, 40, 80, and 120 µM was found to induce apoptosis of cancer cells of nine different cancer cell lines, i.e., colon, prostate, breast, and ovarian carcinomas. These results were confirmed in animal model, as mice bearing colon and breast cancers exhibited a significant reduction of tumors in groups treated with quercetin. Apigenin, a common dietary flavonoid, present in many fruits and vegetables was recently widely investigated for its anticancer properties. Animal studies showed significant reduction of proliferation, invasion, and migration and increased apoptosis of colonorectal, breast, prostate, melanoma, renal cell, and ovarian cancers. Hesperidin, a flavonoid derived from citrus fruit, was reported to inhibit human hepatic cancer HepG2 cells growth through the activation of caspase-9, -8, and -3, downregulation of Bcl-xL protein, and upregulation of Bax, Bak, and tBid protein levels in a dose-dependent manner. It was interesting that the sensitivity of HepG2 cancer cells to hesperidin was much higher compared to naringin, neohesperidin, and naringenin. Other in vitro experiments, performed on MCF-7 human breast, androgen-independent PC-3, and DU-145 prostate cancer cells, and androgen-dependent LNCa cancer cells, revealed significant antitumor effect of hesperidin. The mechanism of action was different to antimitosis and involved inhibition of the proliferation of MCF-7-GFP-Tubulin cells and both basal and testosterone-induced proliferation of LNCaP cells. Hesperidin was also proved to inhibit ovarian cancer cell viability and increase cytotoxicity in a dose- and time-dependent manner. The mechanism of action involved induction of apoptosis through activation of protein expression of antigrowth arrest- and DNA damage-inducible gene 153, anti-CCAAT’enhancer-binding protein homologous protein, glucose-regulated protein 78, and cytochrome c. This mechanism may shed new light on a potential role of this dietary flavonoid in the prediction of ovarian carcinoma.

4.4. Cardiovascular Diseases Prevention

A population-based cohort study performed by Pozzo and coworkers over 12 years on 1658 individuals showed that higher dietary intake of flavonoids was associated with reduced risk of CVDs after a mean 12-year follow-up and a 40–50% lower risk of nonfatal CV events. No influence of different subclasses of flavonoids on CV diseases prevention was observed. The intake of flavan-3-ols, anthocyanidins, and flavanones were the most significantly inversely associated with all-cause mortality. Although results from numerous studies and RCTs are inconclusive, a recent meta-analysis performed by Sarrias and coworkers (based on 117 articles published between 1997–2015) revealed significant effect of flavanols on blood lipids. Flavanols from tea, cocoa, and apples (catechins and dimeric procyanidins) were proved to significantly reduce total and LDL cholesterol and increase HDL fraction. No influence on TAGs level was observed.

During the last 10 years, several studies and clinical trials have confirmed that catechins have strong antihypertensive activity. The mechanism involves regulation of NADPH production and inhibition of RNA expression of Il-6 and MMP-9 in blood patients with hypertension. Bogdanski and co-investigators in a double-blind, placebo-controlled trial on 56 obese, hypertensive subjects, revealed that green tea polyphenols are effective in reduction of both systolic and diastolic blood pressures. Additionally, increased intake of these flavonoids caused significant reduction of TNF-α, C-reactive protein levels, fasting serum glucose, insulin levels, and insulin resistance.

Rats treated for five weeks with-epicatechin at 2 or 10 mg/kg per day were shown to be resistant to a systolic blood pressure increase caused by administration of deoxycorticosterone acetate (DOCA). Epicatechin was proved to improve the impaired endothelium-dependent relaxation response to acetylcholine and reduce plasma endothelin-1 and malondialdehyde levels. Among other catechins, EGCG was especially responsible for the inhibition of calcium-activated chloride channels. Further, based on that mechanism, calcium dependent phosphorylation of inositol triphosphate, calmodulin antibodies, and calmodulin-dependent protein kinase II were improved, which resulted in strong antihypertensive effect. Studies performed on spontaneously hypertensive rats revealed significant decrease of blood pressure after administration of EGCG (200 mg/kg/day). The effect was comparable to observed after treatment with 3 mg/kg/day of enalapril—a common hypotensive drug. Moreover, it was shown that EGCG increased production and release of nitric oxide from endothelium via a PI-3-kinase pathway. Obtained results suggested that EGCG may play beneficial role in the treatment of hypertension and metabolic syndrome. EGCG was also proved to inhibit renin—a crucial enzyme in the treatment of hypertension. This in vitro study also revealed that the specific structure of EGCG—a galloyl moiety and ortho-trihydroxy phenyl structure—may be responsible for the inhibitory activity of EGCG towards renin.

Catechins can also play a beneficial role in the prevention of hypertension through the increased release of NO, which is endogenous relaxing factor, responsible, among others, for lowering blood pressure. EC was proved to increase the activity of endogenous NO synthetase, protect endothelial cells from strong stress, and stabilize EDRF (endothelium-derived relaxing factor) when blood vessels are damaged.

4.5. Anti-Obesity Effect/Weight-Reducing Properties

According to Huang and coworkers, until 2013 there were about 24 different clinical trials performed on obese participants, which have proved the weight-reducing properties of tea polyphenols. Numerous studies performed in vitro and on animals have also confirmed beneficial effects of green tea infusions on weight reduction. The precise molecular mechanism is still discussed. However, the key findings involve reduction of food intake, deterioration of lipid emulsification and absorption, adipogenesis and lipid synthesis suppression, and increase of energy expenditure via thermogenesis. Acceleration of fat oxidation and fecal lipid excretion were also confirmed. As a result, total body mass, fat tissue content, and waist to hip ratio were reduced. Blood lipids levels were also improved. Not only flavan-3-ols present in tea, but also other flavonoids present in commonly consume foods may have a positive effect on the reduction of the body weight. Supplementation with a mixture of quercetin and green tea extract for four weeks in mice fed a high fat diet for 12 weeks revealed significant changes in genes expression. Over 100 genes in adipose tissue were downregulated, including those involved in leukocyte extravasation and phagocytosis. Downregulation of cholesterol metabolism was also observed and cholesterol congeries in adipose and muscle tissue is frequently observed in obesity and sarcopenia. A mild improvement of glucose tolerance in animals fed with quercetin only was proved. This study confirmed other findings suggesting an important role of quercetin, which improved blood glucose tolerance and insulin sensitivity. Quercetin was also shown to regulate hepatic gene expression related to lipid metabolism in high-fat diet (HFD)-induced obesity in mice. The supplementation with this dietary flavonoid caused significant reduction of liver and white adipose tissue weight as well as hepatic lipid accumulation. Moreover, the size of lipid droplets in the animal epididymal fat pads was also decreased.

Luteolin, was also found to increase insulin sensitivity and decrease low-grade chronic inflammation observed in the obesity through the enhanced uptake of glucose by adipocytes and reduction of proinflammatory chemokines blood levels. Moreover, luteolin treatment decreased mRNA levels of tumor necrosis factor α, IL-6, and MCP-1, while it increased the gene expression of adiponectin and leptin in 3T3-L1 adipocytes and primary mouse adipose cells. A potent transcriptional activation of PPARγ (peroxisome proliferator-associated receptor) target genes in animal adipose cells was also revealed.

4.6. Antidiabetic Activity

Diabetes is the only disease that in the twentieth first century was referred to as an epidemic by the United Nations. It is the most frequently observed chronic noncommunicable disease, which is a major public health problem worldwide. Over 9% of adults have diabetes, which corresponds to 415 million people. Since diabetes is a dominant cause of mortality, morbidity, disability, and increasing healthcare expenditures, this disease is one of the biggest medical challenges of the present time. Several antioxidant, anti-inflammatory, and increasing the insulin sensitivity activities of dietary polyphenols were described above. However, in recent years, many different properties of phenolics towards the regulation of carbohydrates metabolism have been described in the scientific literature. Apigenin, a flavone commonly present in celery, red pepper, parsley, and lemon, was described to have beneficial effects on AMP-dependent regulation of lipid and glucose metabolism. Apigenin was found to be a 200-fold more potent AMPK (5’ adenosine monophosphate-activated protein kinase) activator compared to metformin, a well-known antidiabetes drug. Apigenin administrated intraperitoneally for seven days (4 mg/kg body weight/day) had a strong antihyperglycemic effect in mice with STZ (streptozocin)-induced diabetes. This effect was more marked in the oral glucose tolerance test. The protective effect of these compounds over liver and kidneys of STZ-diabetic models was also shown. Another study showed that apigenin increased glucose uptake, thyroid hormones level, and insulin secretion in alloxan-induced diabetic mice. Increased level of glucose led to intensified toxicity, which contributes to progressive pancreatic β-cell failure and the development of overt diabetes. Increased production of ROS is one of the major aspects of glucose toxicity. A study performed on HIT-T15 pancreatic β-cells subjected to oxidative stress caused by 2-deoxy-D-ribose (dRib) revealed the protective effect of apigenin against cell damage. The results revealed that this dietary flavonoid caused significant reduction of the intracellular ROS level, increased cell survival and mitochondrial membrane potential, and decreased cell apoptosis. Taken together, it was concluded that administration of apigenin attenuated all the pancreatic β-cell failures caused by dRib. Naringin and naringenin (the aglycone form of naringin), the most abundant representatives of flavanones in foods, possess a wide spectrum of antidiabetic activity. In mice with type 2 diabetes, naringin and hesperidin, which were separately administrated, significantly influenced glycolysis and gluconeogenesis and thus improved hyperglycemia. The proposed mechanism involved the upregulation of hepatic and adipocyte PPARγ and GLUT 4, important for the regulation of glucose metabolism. Additionally, both flavonoids improved lipid metabolism by reducing free fatty acid and TAGs (Triglycerides) plasma levels, inhibition of hepatic (HMG-CoA) reductase activity, and increasing fecal cholesterol. On the other hand, recent findings on rodents suggest that naringenin and quercetin attenuates glucose uptake in adipose tissue, thus deteriorating glucose metabolism. This was observed after oral administration of these two dietary flavonoids in the amount equal to a consumption of a one glass of grapefruit juice. Glucose tolerance impairment was probably due to inhibition of hypothalamic PI3K signaling, an enzyme which is crucial for the neuronal control of glucose homoeostasis in the organism. These inconclusive actions may be due to individuals’ differences in absorption and metabolism of these polyphenols. Recently, several studies revealed that diet supplementation with hesperidin in db/db, C57BL6 mice resulted in the regulation of hepatic enzymes involved in glucose metabolism in liver, which finally improved hyperglycemia. The reported mechanism was due to the upregulation of hepatic glucokinase, PPARγ, and adipocyte GLUT4. Reduction of G6Pase (glucose-6-phosphatase) and increased expression of GK (glucokinase), which, when combined, decreased glucose export through glucose transporter membrane proteins was observed in rats with STZ-induced type 1 diabetes. Quercetin and its glycosylated forms are another example of the flavonoids which are present in human diet in the highest amounts, for which many findings on their antidiabetic activity were recently described. Berry extract with high quercetin concentration was proved to induced AMPK signaling pathways in muscle tissue and oxygen utilization in mitochondria—an analogous mechanism to that of metformin. Quercetin glycosides like hyperoside or isoquercetin also stimulated AMPK in muscle tissue and improved insulin resistance. High effectiveness of quercetin was also reported in the treatment of STZ-induced diabetes in mice. Significant enhancement of liver glucose uptake and reduction of liver glycogenolysis and gluconeogenesis together was proved. Moreover, depletion of GLUT4 and GK stimulated by hyperglycemia was also observed.

Rutin at the concentration of 100 mg/kg in the diet showed significant reduction in blood glucose levels and increased production of insulin in mice with induced diabetes. Moreover, reestablishment of glycogen content and activities of enzymes involved in carbohydrates metabolism was also proved in this study.

Several studies proved that supplementation of 0.04–0.045% quercetin in the diet significantly reduced serum glucose and insulin resistance, measured as HOMA-IR parameter, in obese rats and a mouse model. No influence on body weight or adipose tissue size was observed. It was also concluded that quercetin is more effective as an antidiabetic than as an anti-obesity agent.

Polyphenolic compounds from green, black, and oolong tea were shown to be strong noncompetitive inhibitors of α-glucosidase—the enzyme responsible for intestinal maltose, maltotriose, and α-dextrin hydrolysis, which increases blood glucose levels. Among the tested products, polyphenols derived from oolong tea were characterized by the strongest inhibitory potential. The study performed by Johnston and coworkers on polarized Caco-2 intestinal cells revealed that catechins from green tea are effective inhibitors of glucose intestinal uptake through regulation of the SGLT-1 and GLUT 2 pathways. The authors concluded that such a mechanism may be beneficial in reducing sugar intestinal absorption and an important dietary tool in the management of diabetes.

4.7. The Activity of Dietary Polyphenols toward CNS Disorders

Neurodegenerative diseases are progressive disorders of the nervous system that are associated with abnormal functioning or destruction of neurons in the brain and/or spinal cord. These diseases are the result of many toxic processes, eventually leading to the death of nerve cells. Factors that may induce neurodegeneration include: deficiency of endogenous antioxidants, inflammation, excitotoxicity of glutamate, expression of proapoptotic proteins, and increases in iron and nitric oxide, leading to oxidative stress. Alzheimer’s and Parkinson’s diseases are considered the most common neurodegenerative disorders.

4.7.1. Parkinson’s Disease

PD (Parkinson’s disease) affects about 1% of the population over the age of 50. Symptoms are caused by degenerative changes of dopaminergic neurons, mainly in the substantia nigra pars compacta with the presence of Lewy bodies and Lewy neurites, which results in a decrease in dopamine concentration. Other neuropathological changes observed in the disease include: activation of microglial cells and increase in α-synuclein concentration. Despite the many hypotheses and speculations about PD etiology, oxidative stress seems to be a crucial factor in the development of the disease. Although the estimation of daily dietary intake of polyphenols is complicated and their bioavailability and the chemical forms in which they directly act in cells are even harder to explain, recent studies have shown that phenolics can cross the blood–brain barrier and exert biological effects in CNS. The precise protective mechanism of polyphenols toward the dopaminergic neurons is still unclear and a matter of discussion. Recent studies have confirmed that their major antioxidant mechanism of action is probably not the only one responsible for cellular protection. Fraga suggests that changes in membrane and protein functioning, even at very low polyphenol concentrations, could significantly change molecular mechanisms and therefore possess important biological activity in vivo. Interactions between polyphenols and proteins, even at concentrations lower than those required to act as an antioxidant, leading to inhibition of protein aggregation, play a key role in the prevention of PD. Several studies during the last decade have proved that polyphenols significantly inhibit the expression of α-synuclein—a key protein in the formation of oligomeric aggregates, which is one of the most important factors in the pathogenesis of PD.

Masuda et al. tested 79 compounds belonging to 12 different chemical classes (including 39 polyphenols) for their potential to inhibit the deposition of α-synuclein into the filaments in vitro. A significant decrease in sarkosyl-insoluble α-synuclein and a corresponding increase in the level of sarkosyl-soluble protein was observed in the presence of exifone, gossypetin, myricetin, and purpurogallin. The most effective polyphenols for the inhibition of α-synuclein filament deposition were baicalein, delphinidin, EGCG, exifone, GC (-gallocatechin), GCG (-gallocatechin gallate), gossypetin, hinokiflavone, hypericin, procyanidin B1, procyanidin B2, rosmarinic acid, and theaflavine. These findings proved that the inhibitory potential of some dietary polyphenols against the formation of insoluble oligomers and reduction of their toxicity to nerve cells may be a crucial mechanism in the prevention of PD development.

In a similar study, Meng et al. investigated the ability of 48 flavonoids belonging to different classes for their effectiveness to inhibit the fibrillation of α-synuclein in vitro. The investigation revealed that the majority of the tested polyphenols inhibit α-synuclein fibrillation and aggregation (e.g., luteolin, rutin, C, ECG (epicatechin-3-gallate)), with EGCG, myricetin, baicalein, eriodictyol, and quercetin being the strongest inhibitors. On the other hand, diosmetin, hesperetin, and hesperidin possessed no inhibitory activity.

Several studies have proved that EGCG can strongly reduce α-synuclein neurocytotoxicity by transforming large, harmful fibrils into smaller, nontoxic, amorphous protein aggregates.

In vitro studies by Lu et al. performed on the rat liver cytosol demonstrated that EGCG is a strong inhibitor of the catechol-O-methyltransferase enzyme (COMT), which can significantly improve the bioavailability of L-Dopa—the most important drug in the therapy of PD.

The protective role of tea polyphenols against neurotoxins has been proved in vivo in mice with MPTP (N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine)-induced Parkinsonism. This study demonstrated that green tea flavonoids, as well as isolated EGCG, strongly decrease striatal dopamine depletion and loss of neurons of the substantia nigra. The neuroprotective role of EGCG was associated with its iron-chelation and antioxidant properties, which led to decreased accumulation of iron and α-synuclein in the substantia nigra pars compacta of the brain.

Another study on a mice model revealed that tea consumption decreases, by about 30–60%, the risk of PD. Oral administration of black tea infusions before or after 6-OHDA (a neurotoxin of dopaminergic system applied to rat neonates which develops persistent brain damage) has been reported to reduce the impairment of dopaminergic neurons and improve motor efficiency.

Since oxidative stress, accumulation of transition metals, and inflammation play key roles in neuronal damage, the strong antioxidant and metal chelating properties of polyphenols also seem to be crucial in the prevention of neurodegenerative disorders. However, other mechanisms are also significant, as presented above.

Although several in vitro or in vivo experiments have demonstrated the beneficial role of polyphenols against PD, there are still little data from epidemiological studies. One of the few such studies is research performed by Checkoway and co-investigators, which proved that consumption of at least two cups of tea per day significantly reduces the risk of PD development. In another study, Gao and coworkers investigated the influence of flavonoid intake on the risk of PD. They concluded that there is a significant negative correlation between a diet rich in flavonoids and PD incidence; however, the protective role of other dietary substances of plant origin also cannot be precluded. They also determined the most important dietary sources of flavonoids in relation to PD, which were berries, red wine, orange/orange juice, and apples (in men), but surprisingly not tea. They also found significant associations between higher anthocyanin intake and PD risk. For other subclasses of flavonoids, such a correlation was not observed.

The pathogenesis of PD is still not clear. Therefore, the future discovery of new findings and mechanisms of action of flavonoids in terms of the prevention of this disease are probably only a matter of time. However, data on the flavonoids dosages necessary to prevent PD incidence and progression and results from clinical studies are currently scarce.

4.7.2. Alzheimer’s Disease

Alzheimer’s disease (AD) is the most common neurodegenerative disorder worldwide and the most frequent observed form of dementia. As reported in 2015, the prevalence of this disease has exceeded 44 million people across the world and it is expected that this number will double by 2050. The abnormal extracellular accumulation of amyloid-β-peptide in amyloid plaques and hyperphosphorylation of tau proteins and their excessive aggregation in intracellular neurofibrillary tangles are considered to be the most important neuropathological features of AD. Additionally, epidemiological and clinical data support other hypotheses of the disease development: the reduction of the choline acetyltransferase activity; impairment of the brain mitochondria functioning; metabolic changes connected with lifestyle diseases such as diabetes or obesity or vascular problems leading to a deterioration in cerebral blood flow.

The positive role of flavonoid-rich products and diets toward the prevention of AD and improving cognitive functions has been extensively described throughout the last 20 years. In general, their mechanism of action is connected with antioxidant activity and thus anti-aging properties. Protective effects of various polyphenols have been confirmed in several experiments regarding the use of single phenolics, as well as total extracts. Joseph et al. revealed that mice fed for eight months with a diet containing blueberry extract (20 g/kg) rich in polyphenols showed a significant improvement in memory and cognitive functions. Polyphenols from the extract enhanced neuronal signaling via the influence on the extracellular signal-regulated kinase and decreased activity of N-Sase (neutral sphingomyelin-specific phospholipase C) in the hippocampus and striatum. The latter enzyme activity increases as a function of age; thus, its inhibition may have a nootropic effect. The authors concluded that a diet rich in antioxidant phytochemicals may overcome genetic predispositions to AD. However, they did not investigate which particular polyphenols were responsible for such activity.

Of all the dietary polyphenols, it seems that the strongest potential in the prevention of AD has been confirmed for EGCG. This main green tea polyphenol, via activation of PKC (protein kinase C), promotes the nonamyloidogenic α-secretase pathway of APP in neuronal cell cultures and thus reduces the formation of β-amyloid fibrils. These results are supported by in vivo studies—a two-week treatment of mice with EGCG revealed a significant decrease in APP production and an increased synthesis of sAPP (soluble form of APP) in the hippocampus.

Another clinical parameter associated with a higher prevalence of AD is homocysteine. Increased levels of this amino acid may be responsible for vascular impairment and further neurotoxic alterations. Higher homocysteine levels are determined in the moderate phase of AD, rather than in initial stage and control groups. Recent findings suggest that consumption of beverages rich in polyphenols may reduce inflammation and vascular impairments associated with AD. Antioxidants decrease the levels of thiol groups (from homocysteine), which are involved in the autocatalytic oxidation process in plasma and increased production of ROS. As a result, lower amounts of free radicals and reduced cell damage are observed. A population-based prospective study preformed on 1836 Japanese-Americans demonstrated that consumption of fruit and vegetable juices at least three times per week significantly delayed the onset of AD, especially among patients who are at high risk of developing the disease. In particular, polyphenols from grapes were emphasized as being active toward the reduction of the disease progression.

Moderate consumption of red wine (rich in stilbenes, ex. resveratrol) has been proved to reduce β-amyloid progression and thus attenuates cognitive impairment and the prevalence of AD.

Table 2 summarizes recent findings on the biological properties of dietary polyphenols, which may be crucial in the potential prevention of lifestyle diseases incidence.

5. Conclusions

Polyphenols are the most common non-nutrients present in the human diet. Considering the significant amounts of compounds consumed in this class and the multitude of their activities, it should be noted that they can play an important role in the prevention of numerous disorders, including civilization diseases. However, it should be remembered that despite many promising results obtained in in vitro or animal experiments regarding their beneficial effects towards the organism, there is still not enough convincing evidence from human studies, especially with large populations. More research of this type is needed to better understand the real value of dietary polyphenols in the context of their ability to prevent the progress of civilization diseases.

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    Csanyi G., Yao M., Rodriguez A.I., Al Ghouleh I., Sharifi-Sanjani M., Frazziano G., Huang X., Kelley E.E., Isenberg J.S., Pagano P.J. Thrombospondin-1 regulates blood flow via CD47 receptor-mediated activation of NADPH oxidase 1. Arterioscler. Thromb. Vasc. Biol. 2012;32:2966-2973.

    Not in our library10.1161/atvbaha.112.300031

  64. 64.

    Touyz R.M., Briones A.M. Reactive oxygen species and vascular biology: Implications in human hypertension. Hypertens. Res. 2011;34:5-14.

    Not in our library10.1038/hr.2010.201

  65. 65.

    Heitzer T., Schlinzig T., Krohn K., Meinertz T., Münzel T. Endothelial dysfunction, oxidative stress, and risk of cardiovascular events in patients with coronary artery disease. Circulation. 2001;104:2673-2678.

    Not in our library10.1161/hc4601.099485

  66. 66.

    Koch W., Baj T., Kukula-Koch W., Marzec Z. Dietary intake of specific phenolic compounds and their effect on the antioxidant activity of daily food rations. Open Chem. 2015;13:869-876.

    Not in our library10.1515/chem-2015-0100

  67. 67.

    Huxley R.R., Neil H.A. The relation between dietary flavonol intake and coronary heart disease mortality: A meta-analysis of prospective cohort studies. Eur. J. Clin. Nutr. 2003;57:904-908.

    Not in our library10.1038/sj.ejcn.1601624

  68. 68.

    Jarząb A., Kukula-Koch W. Recent advances in obesity: The role of turmeric tuber and its metabolites in the prophylaxis and therapeutical strategies. Curr. Med. Chem. 2017;24:1.

    Not in our library10.2174/0929867324666161118095443

  69. 69.

    Chang Y.J., Myung S.-K., Chung S.T., Lee Y.K., Jeon Y.-J., Park C.-H., Seo H.G., Huh B.Y. Effects of vitamin treatment or supplements with purported antioxidant properties on skin cancer prevention: A meta-analysis of randomized controlled trials. Dermatology. 2011;223:36-44.

    Not in our library10.1159/000329439

  70. 70.

    Puertollano M.A., Puertollano E., de Cienfuegos G.Á., de Pablo M.A. Dietary antioxidants: Immunity and host defense. Curr. Top. Med. Chem. 2011;11:1752-1766.

    Not in our library10.2174/156802611796235107

  71. 71.

    Katta R., Brown D.C. Diet and skin cancer: The potential role of dietary antioxidants in nonmelanoma skin cancer prevention. J. Skin Cancer. 2015;893149.

    Not in our library10.1155/2015/893149

  72. 72.

    Lugasi A., Hóvári J., Sági K.V., Bíró L. The role of antioxidant phytonutrients in the prevention of diseases. Acta Biol. Szeged. 2003;47:119-125.

    Not in our library

  73. 73.

    Grosso G., Micek A., Godos J., Pajak A., Sciacca S., Galvano F., Giovannucci E.L. Dietary flavonoid and lignan intake and mortality in prospective cohort studies: Systematic review and dose-response meta-analysis. Am. J. Epidemiol. 2017;1-13.

    Not in our library10.1093/aje/kww207

  74. 74.

    Robbins R.J. Phenolic acids in foods: An overview of analytical methodology. J. Agric. Food Chem. 2003;51:2866-2887.

    Not in our library10.1021/jf026182t

  75. 75.

    Koes R., Verweij W., Quattrocchio F. Flavonoids: A colourful model for the regulation and evolution of biochemical pathways. Trends Plant Sci. 2005;10:236-242.

    Not in our library10.1016/j.tplants.2005.03.002

  76. 76.

    Hertog M.G.L., Hollman P.C.H., Venema D.P. Optimization of a quantitative HPLC determination of potentially anticarcinogenic flavonoids in vegetables and fruits. J. Agric. Food Chem. 1992;40:1591-1598.

    Not in our library10.1021/jf00021a023

  77. 77.

    Yao L.H., Jiang Y.M., Shi J., Tomás-Barberán F.A., Datta N., Singanusong R., Chen S.S. Flavonoids in food and their health benefits. Plant Foods Hum. Nutr. 2004;59:113-122.

    Not in our library10.1007/s11130-004-0049-7

  78. 78.

    Kühnau J. The flavonoids, a class of semi-essential food components: Their role in human nutrition. World Rev. Nutr. Diet. 1976;24:117-191.

    Not in our library10.1159/000399407

  79. 79.

    Tomás-Barberán F.A., Clifford M.N. Flavanones, chalcones and dihydrochalcones-nature, occurrence and dietary burden. J. Sci. Food Agric. 2000;80:1073-1080.

    Not in our library10.1002/(sici)1097-0010(20000515)80:7<1073::aid-jsfa568>3.0.co;2-b

  80. 80.

    Justesen U., Knuthsen P., Leth T. Determination of plant polyphenols in Danish foodstuffs by HPLC-UV and LC-MS detection. Cancer Lett. 1997;114:165-167.

    Not in our library10.1016/s0304-3835(97)04651-x

  81. 81.

    Knekt P., Jarvinen R., Revnanen A., Moatela J. Flavonoid intake and coronary mortality in Finland: A cohort study. BMJ. 1996;312:478-481.

    Not in our library10.1136/bmj.312.7029.478

  82. 82.

    Hertog M.G.L., Kromhout D., Aravanis C., Blackburn H., Buzina R., Fidanza F., Giampaoli S., Jansen A., Menotti A., Nedeljkovic S. Flavonoid intake and long term risk of coronary heart disease and cancer in the Seven Countries Study. Arch. Intern. Med. 1995;155:381-386.

    Not in our library10.1001/archinte.1995.00430040053006

  83. 83.

    Rimm E.B., Katan M.B., Ascherio A., Stampfer M.J., Willett W.C. Relation between intake of flavonoids and risk for coronary heart disease in male health professionals. Ann. Intern. Med. 1996;12:384-389.

    Not in our library10.7326/0003-4819-125-5-199609010-00005

  84. 84.

    Pozzo V., Goitre I., Fadda M., Gambion R., De Francesco A., Soldati L., Gentile L., Magistroni P., Cassader M., Bo S. Dietary flavonoid intake and cardiovascular risk: A population-based cohort study. J. Transl. Med. 2015;13:218.

    Not in our library10.1186/s12967-015-0573-2

  85. 85.

    Pérez-Jiménez J., Neveu V., Vos F., Scalbert A. A systematic analysis of the content of 502 polyphenols in 452 foods and beverages—An application of the Phenol-Explorer database. J. Agric. Food Chem. 2010;58:4959-4969.

    Not in our library10.1021/jf100128b

  86. 86.

    Neveu V., Pérez-Jiménez J., Vos F., Crespy V., Du Chaffaut L., Mennen L., Knox C., Eisner R., Cruz J., Wishart D., et al. Phenol-Explorer: An online comprehensive database on polyphenol contents in foods. Database. 2010;2010:bap024.

    Not in our library10.1093/database/bap024

  87. 87.

    Pérez-Jiménez J., Neveu V., Vos F., Scalbert A. Identification of the 100 richest dietary sources of polyphenols: An application of the Phenol-Explorer database. Eur. J. Clin. Nutr. 2010;64:112-120.

    Not in our library10.1038/ejcn.2010.221

  88. 88.

    Mishra A., Kumar S., Pandey A.K. Scientific validation of the medicinal efficacy of Tinospora cordifolia. Sci. World. J. 2013;292934.

    Not in our library10.1155/2013/292934

  89. 89.

    Kukula-Koch W., Aligiannis N., Halabalaki M., Skaltsounis A.L., Glowniak K., Kalpoutzakis E. Influence of extraction procedures on phenolic content and antioxidant activity of Cretan barberry herb. Food Chem. 2013;138:406-413.

    Not in our library10.1016/j.foodchem.2012.10.045

  90. 90.
  91. 91.

    Pinto M.S. Tea: A new perspective on health benefits. Food Res. Int. 2013;53:558-567.

    Not in our library10.1016/j.foodres.2013.01.038

  92. 92.

    Bruno R.S., Bomser J.A., Ferruzzi M.G., Preedy V.R. Antioxidant Capacity of Green Tea (Camellia sinensis). Processing and Impact on Antioxidants in Beverages. 2014.

    Not in our library

  93. 93.

    Kukula-Koch W., Koch W., Angelis A., Halabalaki M., Aligiannis N. Application of pH-zone refining hydrostatic countercurrent chromatography (hCCC) for the recovery of antioxidant phenolics and the isolation of alkaloids from Siberian barberry herb. Food Chem. 2016;203:394-401.

    Not in our library10.1016/j.foodchem.2016.02.096

  94. 94.

    Sung H., Nah J., Chun S., Park H., Yang S.E., Min W.K. In vivo antioxidant effect of green tea. Eur. J. Clin. Nutr. 2000;54:527-529.

    Not in our library10.1038/sj.ejcn.1600994

  95. 95.

    Arent S.M., Senso M., Golem D.L. The effects of theaflavin-enriched black tea extract on muscle soreness, oxidative stress, inflammation, and endocrine responses to acute anaerobic interval training: A randomized, double-blind, crossover study. J. Int. Soc. Sport. Nutr. 2010;7:11.

    Not in our library10.1186/1550-2783-7-11

  96. 96.
  97. 97.

    Tsai P.H., Kan N.B., Ho S.C., Liu C.C., Lin C.C. Effects of oolong tea supplementationon lipid peroxidation of athletes at rest and post-exhaustive exercise. J. Food Sci. 2005;70:581-585.

    Not in our library10.1111/j.1365-2621.2005.tb08332.x

  98. 98.

    Weerawatanakorn M., Hung W.-L., Pan M.-H., Li S., Li D., Wan X., Ho C.-T. Chemistry and health beneficial effects of oolong tea and theasinensins. Food Sci. Hum. Well. 2015;4:133-146.

    Not in our library10.1016/j.fshw.2015.10.002

  99. 99.

    Pae M., Wu D. Immunomodulating effect of epigallocatechin-3-gallate from green tea: Mechanisms and applications. Food Funct. 2013;4:1287-1303.

    Not in our library10.1039/c3fo60076a

  100. 100.

    Wu D. Green tea EGCG, T-cell function, and T-cell-mediated autoimmune encephalomyelitis. J. Investig. Med. 2016;64:1213-1219.

    Not in our library10.1136/jim-2016-000158

  101. 101.

    Lee S.Y., Jung Y.O., Ryu J.G., Oh H.J., Son H.J., Lee S.H., Kwon J.E., Kim E.K., Park M.K., Park S.H., et al. Epigallocatechin-3-gallate ameliorates autoimmune arthritis by reciprocal regulation of T helper-17 regulatory T cells and inhibition of osteoclastogenesis by inhibiting STAT3 signaling. J. Leucoc. Biol. 2016;100:559-568.

    Not in our library10.1189/jlb.3a0514-261rr

  102. 102.

    Nikfarjam B.A., Adineh M., Hajiali F., Nassiri-Asl M. Treatment with rutin—A therapeutic strategy for neutrophil-mediated inflammatory and autoimmune diseases: Anti-inflammatory effects of rutin on neutrophils. J. Pharmacopunct. 2017;20:52-56.

    Not in our library10.3831/kpi.2017.20.003

  103. 103.

    Nikfarjam B.A., Hajiali F., Adineh M., Nassiri-Asl M. Anti-inflammatory Effects of Quercetin and Vitexin on Activated Human Peripheral Blood Neutrophils. J. Pharmacopunct. 2017;20:127-131.

    Not in our library10.3831/kpi.2017.20.017

  104. 104.

    Zhang S., Liu X., Sun C., Yang J., Wang L., Liu J., Gong L., Jing Y. Apigenin attenuates experimental autoimmune myocarditis by modulating Th1/Th2 cytokine balance in mice. Inflammation. 2016;39:678-686.

    Not in our library10.1007/s10753-015-0294-y

  105. 105.

    Zhang Y., Duan W., Owusu L., Wu D., Xin Y. Epigallocatechin-3-gallate induces the apoptosis of hepatocellular carcinoma LM6 cells but not non-cancerous liver cells. Int. J. Mol. Med. 2015;35:117-124.

    Not in our library10.3892/ijmm.2014.1988

  106. 106.

    Sur S., Pal D., Roy R., Barua A., Roy A., Saha P., Panda C.K. Tea polyphenols EGCG and TF restrict tongue and liver carcinogenesis simultaneously induced by N-nitrosodiethylamine in mice. Toxicol. Appl. Pharmacol. 2016;300:34-46.

    Not in our library10.1016/j.taap.2016.03.016

  107. 107.

    Kalra N., Seth K., Prasad S., Singh M., Pant A.B., Shukla Y. Theaflavins induced apoptosis of LNCaP cells is mediated through induction of p53, down-regulation of NF-kappa B and mitogen-activated protein kinases pathways. Life Sci. 2007;80:2137-2146.

    Not in our library10.1016/j.lfs.2007.04.009

  108. 108.

    Prasad S., Kaur J., Roy P., Kalra N., Shukla Y. Theaflavins induce G2/M arrest by modulating expression of p21waf1/cip1, cdc25C and cyclin B in human prostate carcinoma PC-3 cells. Life Sci. 2007;81:1323-1331.

    Not in our library10.1016/j.lfs.2007.07.033

  109. 109.

    He H.-F. Research progress on theaflavins: Efficacy, formation, and preparation. Food Nutr. Res. 2017;61:1344521.

    Not in our library10.1080/16546628.2017.1344521

  110. 110.

    Song W., Zhao X., Xu J., Zhang H. Quercetin inhibits angiogenesis-mediated human retinoblastoma growth by targeting vascular endothelial growth factor receptor. Oncol. Lett. 2017;14:3343-3348.

    Not in our library10.3892/ol.2017.6623

  111. 111.

    Hashemzaei M., Far A.D., Yari A., Heravi R.E., Tabrizian K., Taghdisi S.M., Sadegh S.E., Tsarouhas K., Kouretas D., Tzanakakis G., et al. Anticancer and apoptosis-inducing effects of quercetin in vitro and in vivo. Oncol. Rep. 2017;38:819-828.

    Not in our library10.3892/or.2017.5766

  112. 112.

    Dai J., Van Wie P.G., Fai L.Y., Kim D., Wang L., Poyil P., Luo J., Zhang Z. Downregulation of NEDD9 by apigenin suppresses migration, invasion, and metastasis of colorectal cancer cells. Toxicol. Appl. Pharmacol. 2016;311:106-112.

    Not in our library10.1016/j.taap.2016.09.016

  113. 113.

    Tseng T.H., Chien M.H., Lin W.L., Wen Y.C., Chow J.M., Chen C.K., Kuo T.C., Lee W.J. Inhibition of MDA-MB-231 breast cancer cell proliferation and tumor growth by apigenin through induction of G2/M arrest and histone H3 acetylation-mediated p21WAF1/CIP1 expression. Environ. Toxicol. 2017;32:434-444.

    Not in our library10.1002/tox.22247

  114. 114.

    Shukla S., Fu P., Gupta S. Apigenin induces apoptosis by targeting inhibitor of apoptosis proteins and Ku70-Bax interaction in prostate cancer. Apoptosis. 2014;19:883-894.

    Not in our library10.1007/s10495-014-0971-6

  115. 115.

    Shukla S., Shankar E., Fu P., MacLennan G.T., Gupta S. Suppression of NF-κB and NF-κB-Regulated gene expression by apigenin through IκBα and IKK pathway in TRAMP mice. PLoS ONE. 2015;10:e0138710.

    Not in our library10.1371/journal.pone.0138710

  116. 116.

    Cao H.H., Chu J.H., Kwan H.Y., Su T., Yu H., Cheng C.Y., Fu X.Q., Guo H., Li T., Tse A.K., et al. Inhibition of the STAT3 signaling pathway contributes to apigenin-mediated anti-metastatic effect in melanoma. Sci. Rep. 2016;6:21731.

    Not in our library10.1038/srep21731

  117. 117.

    Hu X.W., Meng D., Fang J. Apigenin inhibited migration and invasion of human ovarian cancer A2780 cells through focal adhesion kinase. Carcinogenesis. 2008;29:2369-2376.

    Not in our library10.1093/carcin/bgn244

  118. 118.

    Meng S., Zhu Y., Li J.F., Wang X., Liang Z., Li S.Q., Xu X., Chen H., Liu B., Zheng X.Y., et al. Apigenin inhibits renal cell carcinoma cell proliferation. Oncotarget. 2017;8:19834-19842.

    Not in our library10.18632/oncotarget.15771

  119. 119.

    Banjerdpongchai R., Wudtiwai B., Khaw-on P., Rachakhom W., Duangnil N., Kongtawelert P. Hesperidin from Citrus seed induces human hepatocellular carcinoma HepG2 cell apoptosis via both mitochondrial and death receptor pathways. Tumour Biol. 2016;37:227-237.

    Not in our library10.1007/s13277-015-3774-7

  120. 120.

    Lee C.J., Wilson L., Jordan M.A., Nguyen V., Tang J., Smiyun G. Hesperidin suppressed proliferations of both human breast cancer and androgen-dependent prostate cancer cells. Phytother. Res. 2010;24:15-19.

    Not in our library10.1002/ptr.2856

  121. 121.

    Zhao J., Li Y., Gao J., De Y. Hesperidin inhibits ovarian cancer cell viability through endoplasmic reticulum stress signaling pathways. Oncol. Lett. 2017;14:5569-5574.

    Not in our library10.3892/ol.2017.6873

  122. 122.

    González-Sarrías A., Combet E., Pinto P., Mena P., Dall’Asta M., Garcia-Aloy M., Rodríguez-Mateos A., Gibney E.R., Dumont J., Massaro M., et al. A systematic review and meta-analysis of the effects of flavanol-containing tea, cocoa and apple products on body composition and blood lipids: Exploring the factors responsible for variability in their efficacy. Nutrients. 2017;9:746.

    Not in our library10.3390/nu9070746

  123. 123.

    Bogdanski P., Suliburska J., Szulinska M., Stepien M., Pupek-Musialik D., Jablecka A. Green tea extract reduces blood pressure, inflammary biomarkers, and oxidative stress and improves, parameters associated with insulin resistance in obese, hypertensive patients. Nutr. Res. 2012;32:421-427.

    Not in our library10.1016/j.nutres.2012.05.007

  124. 124.

    Ademiluyi A.O., Oboh G., Ogunsuyi O.B., Oloruntoba F.M. A comparative study on antihypertensive and antioxidant properties of phenolic extracts from fruit and leaf of some guava (Psidium guajava L.) varieties. Comp. Clin. Pathol. 2016;25:363-374.

    Not in our library10.1007/s00580-015-2192-y

  125. 125.

    Tounekti T., Joubert E., Hernandez I., Munne-Bosch S. Improving the polyphenol content of tea. Crit. Rev. Plant Sci. 2013;32:192-215.

    Not in our library10.1080/07352689.2012.747384

  126. 126.

    Gómez-Guzmán M., Jiménez R., Sánchez M., Zarzuelo M.J., Galindo P., Quintela A.M., Lopez-Sepulveda R., Romero M., Tamargo J., Vargas F., et al. Epicatechin lowers blood pressure, restores endothelial function, and decreases oxidative stress and endothelin-1 and NADPH oxidase activity in DOCA-salt hypertension. Free Radic. Biol. Med. 2012;52:70-79.

    Not in our library10.1016/j.freeradbiomed.2011.09.015

  127. 127.

    Mahajan N., Dhawan V., Sharma G., Jain S., Kaul D. Induction of inflammatory gene expression by THP-1 macrophages cultured in normocholesterolaemic hypertensive sera and modulatory effects of green tea polyphenols. J. Hum. Hypertens. 2008;22:141-143.

    Not in our library10.1038/sj.jhh.1002277

  128. 128.

    Chen X.Q., Hu T., Han Y., Huang W., Yuan H.B., Zhang Y.T., Du Y., Jiang Y.W. Preventive Effects of Catechins on Cardiovascular Disease. Molecules. 2016;21:1759.

    Not in our library10.3390/molecules21121759

  129. 129.

    Namkung W., Thiagarajah J.R., Phuan P.W., Verkman A.S. Inhibition of Ca2+-activated Cl¯ channels by gallotannins as a possible molecular basis for health benefits of red wine and green tea. FASEB J. 2010;24:4178-4186.

    Not in our library10.1096/fj.10-160648

  130. 130.

    Ohno S., Yokoi H., Mori K., Kasahara M., Kuwahara K., Fujikura J., Naito M., Kuwabara T., Imamaki H., Ishii A., et al. Ablation of the N-type calcium channel ameliorates diabetic nephropathy with improved glycemic control and reduced blood pressure. Sci. Rep. 2016;6:27192.

    Not in our library10.1038/srep27192

  131. 131.

    Potenza M.A., Marasciulo F.L., Tarquinio M., Tiravanti E., Colantuono G., Federici A., Kim J.A., Quon M.J., Montagnani M. EGCG, a green tea polyphenol, improves endothelial function and insulin sensitivity, reduces blood pressure, and protects against myocardial I/R injury in SHR. Am. J. Physiol. Endocrinol. Metab. 2007;292:1378-1387.

    Not in our library10.1152/ajpendo.00698.2006

  132. 132.

    Li F., Takahashi Y., Yamaki K. Inhibitory effect of catechin-related compounds on renin activity. Biomed. Res. 2013;34:167-171.

    Not in our library10.2220/biomedres.34.167

  133. 133.

    Huang J., Wang Y., Xie Z., Zhou Y., Zhang Y., Wan X. The anti-obesity effects of green tea in human intervention and basic molecular studies. Eur. J. Clin. Nutr. 2014;68:1075-1087.

    Not in our library10.1038/ejcn.2014.143

  134. 134.

    Moon H.S., Lee H.G., Choi Y.J., Kim T.G., Cho C.S. Proposed mechanisms of (-)-epigallocatechin-3-gallate for anti-obesity. Chem. Biol. Interact. 2007;167:85-98.

    Not in our library10.1016/j.cbi.2007.02.008

  135. 135.

    Bose M., Lambert J.D., Ju J., Reuhl K.R., Shapses S.A., Yang C.S. The major green tea polyphenol, (-)-epigallocatechin-3 gallate, inhibits obesity, metabolic syndrome, and fatty liver disease in high-fat-fed mice. J. Nutr. 2008;138:1677-1683.

    Not in our library10.1093/jn/138.9.1677

  136. 136.

    Nagao T., Hase T., Tokimitsu I. A green tea extract high in catechins reduces body fat and cardiovascular risks in humans. Obesity. 2007;15:1473-1483.

    Not in our library10.1038/oby.2007.176

  137. 137.

    Mehta V., Parashar A., Sharma A., Singh T.R., Udayabanu M. Quercetin ameliorates chronic unpredicted stress-mediated memory dysfunction in male Swiss albino mice by attenuating insulin resistance and elevating hippocampal GLUT4 levels independent of insulin receptor expression. Horm Behav. 2017;89:13-22.

    Not in our library10.1016/j.yhbeh.2016.12.012

  138. 138.

    Cialdella-Kam L., Ghosh S., Meaney M.P., Knab A.M., Shanely R.A., Nieman D.C. Quercetin and green tea extract supplementation downregulated genes related to tissue inflammatory responses to a 12-week high fat-diet in mice. Nutrients. 2017;9:773.

    Not in our library10.3390/nu9070773

  139. 139.

    Henagan T.M., Lenard N.R., Gettys T.W., Stewart L.K. Dietary quercetin supplementation in mice increases skeletal muscle PGC1alpha expression, improves mitochondrial function and attenuates insulin resistance in a time-specific manner. PLoS ONE. 2014;9:e89365.

    Not in our library10.1371/journal.pone.0089365

  140. 140.

    Jung C.H., Cho I., Ahn J., Jeon T.-I., Ha T.-Y. Quercetin reduces high-fat diet-induced fat accumulation in the liver by regulating lipid metabolism genes. Phytother. Res. 2013;27:139-143.

    Not in our library10.1002/ptr.4687

  141. 141.

    Ding L., Jin D., Chen X. Luteolin enhances insulin sensitivity via activation of PPARγ transcriptional activity in adipocytes. J. Nutr. Biochem. 2010;21:941-947.

    Not in our library10.1016/j.jnutbio.2009.07.009

  142. 142.

    Jaacks L.M., Siegel K.R., Gujral U.P., Narayan K.M. Type 2 diabetes: A 21st century epidemic. Best Pract. Res. Clin. Endocrinol. Metab. 2016;30:331-343.

    Not in our library10.1016/j.beem.2016.05.003

  143. 143.

    Rauter A.P., Martins A., Borges C., Mota-Filipe H., Pinto R., Sepodes B., Justino J. Antihyperglycaemic and protective effects of flavonoids on streptozotocin-induced diabetic rats. Phytother. Res. 2010;24:133-138.

    Not in our library10.1002/ptr.3017

  144. 144.

    Zang M., Xu S., Maitland-Toolan K.A., Zuccollo A., Hou X., Jiang B., Wierzbicki M., Verbeuren T.J., Cohen R.A. Polyphenols stimulate amp-activated protein kinase, lower lipids, and inhibit accelerated atherosclerosis in diabetic ldl receptor-deficient mice. Diabetes. 2006;55:2180-2191.

    Not in our library10.2337/db05-1188

  145. 145.
  146. 146.

    Panda S., Kar A. Apigenin (4′,5,7-trihydroxyflavone) regulates hyperglycaemia, thyroid dysfunction and lipid peroxidation in alloxan induced diabetic mice. J. Pharm. Pharmacol. 2007;59:1543-1548.

    Not in our library10.1211/jpp.59.11.0012

  147. 147.

    Suh K.S., Oh S., Woo J.-T., Kim S.-W., Kim J.-W., Kim Y.S., Chon S. Apigenin attenuates 2-deoxy-d-ribose-induced oxidative cell damage in HIT-T15 pancreatic. β-cells. Biol. Pharm. Bull. 2012;35:121-126.

    Not in our library10.1248/bpb.35.121

  148. 148.

    Jung U.J., Lee M.K., Park Y.B., Kang M.A., Choi M.S. Effect of citrus flavonoids on lipid metabolism and glucose-regulating enzyme mRNA levels in type-2 diabetic mice. Int. J. Biochem. Cell Biol. 2006;38:1134-1145.

    Not in our library10.1016/j.biocel.2005.12.002

  149. 149.

    Pu P., Gao D.-M., Mohamed S., Chen J., Zhang J., Zhou X.-Y., Zhou N.-J., Xie J., Jiang H. Naringin ameliorates metabolic syndrome by activating amp-activated protein kinase in mice fed a high-fat diet. Arch. Biochem. Biophys. 2012;518:61-70.

    Not in our library10.1016/j.abb.2011.11.026

  150. 150.

    Koch C.E., Ganjam G.K., Steger J., Legler K., Stohr S., Schumacher D., Hoggard N., Heldmaier G., Tups A. The dietary flavonoids naringenin and quercetin acutely impair glucose metabolism in rodents possibly via inhibition of hypothalamic insulin signalling. Br. J. Nutr. 2013;109:1040-1051.

    Not in our library10.1017/s0007114512003005

  151. 151.

    Akiyama S., Katsumata S., Suzuki K., Ishimi Y., Wu J., Uehara M. Dietary hesperidin exerts hypoglycemic and hypolipidemic effects in streptozotocin-induced marginal type 1 diabetic rats. J. Clin. Biochem. Nutr. 2010;46:87-92.

    Not in our library10.3164/jcbn.09-82

  152. 152.

    Jung U.J., Lee M.-K., Jeong K.-S., Choi M.-S. The hypoglycemic effects of hesperidin and naringin are partly mediated by hepatic glucose-regulating enzymes in C57BL/KsJ-db/db mice. J. Nutr. 2004;134:2499-2503.

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    Agrawal Y.O., Sharma P.K., Shrivastava B., Ojha S., Upadhya H.M., Arya D.S., Goyal S.N. Hesperidin produces cardioprotective activity via PPAR- pathway in ischemic heart disease model in diabetic rats. PLoS ONE. 2014;9:e111212.

    Not in our library10.1371/journal.pone.0111212

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    Eid H.M., Martineau L.C., Saleem A., Muhammad A., Vallerand D., Benhaddou-Andaloussi A., Nistor L., Afshar A., Arnason J.T., Haddad P.S. Stimulation of AMP-activated protein kinase and enhancement of basal glucose uptake in muscle cells by quercetin and quercetin glycosides, active principles of the antidiabetic medicinal plant vaccinium vitis-idaea. Mol. Nutr. Food Res. 2010;54:991-1003.

    Not in our library10.1002/mnfr.200900218

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    Alam M.M., Meerza D., Naseem I. Protective effect of quercetin on hyperglycemia, oxidative stress and DNA damage in alloxan induced type 2 diabetic mice. Life Sci. 2014;109:8-14.

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    Kobori M., Masumoto S., Akimoto Y., Takahashi Y. Dietary quercetin alleviates diabetic symptoms and reduces streptozotocin-induced disturbance of hepatic gene expression in mice. Mol. Nutr. Food Res. 2009;53:859-868.

    Not in our library10.1002/mnfr.200800310

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    Xu M., Hu J., Zhao W., Gao X., Jiang C., Liu K., Liu B., Huang F. Quercetin differently regulates insulin-mediated glucose transporter 4 translocation under basal and inflammatory conditions in adipocytes. Mol. Nutr. Food Res. 2014;58:931-941.

    Not in our library10.1002/mnfr.201300510

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    Prince P., Kamalakkannan N. Rutin improves glucose homeostasis in streptozotocin diabetic tissues by altering glycolytic and gluconeogenic enzymes. J. Biochem. Mol. Toxicol. 2006;20:96-102.

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    Jeong S.M., Kang M.J., Choi H.N., Kim J.H., Kim J.I. Quercetin ameliorates hyperglycemia and dyslipidemia and improves antioxidant status in type 2 diabetic db/db mice. Nutr. Res. Pract. 2012;6:201-207.

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    Arias N., Macarulla M.T., Aguirre L., Martinez-Castano M.G., Portillo M.P. Quercetin can reduce insulin resistance without decreasing adipose tissue and skeletal muscle fat accumulation. Genes Nutr. 2014;9:361.

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    Yang X., Kong F. Evaluation of the in vitro α-glucosidase inhibitory activity of green tea polyphenols and different tea types. J. Sci. Food Agric. 2016;96:777-782.

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    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.

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    Mandel S., Grunblatt E., Riederer P., Gerlach M., Levites Y., Youdim M.B.H. Neuroprotective strategies in Parkinson’s disease: An update on progress. CNS Drugs. 2003;17:729-762.

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    Berg D., Gerlach M., Youdim M.B.H., Double K.L., Zecca L., Riederer P., Becker G. Brain iron pathways and their relevance to Parkinson’s disease. J. Neurochem. 2001;79:225-236.

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    Dauer W., Przedborski S. Parkinson’s disease: Mechanisms and models. Neuron. 2003;39:889-909.

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    Cardoso S.M., Moreira P.I., Agostinho P., Pereira C., Oliveira C.R. Neurodegenerative pathways in Parkinson’s disease: Therapeutic strategies. Curr. Drug Targets CNS Neurol. Disord. 2005;4:405-419.

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    Braak H., Ghebremedhin E., Rüb U., Bratzke H., Del Tredici K. Stages in the development of Parkinson’s disease-related pathology. Cell Tissue Res. 2004;318:121-134.

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    McGeer P.L., Itagaki S., Akiyama H., McGeer E.G. Rate of cell death in parkinsonism indicates active neuropathological process. Ann. Neurol. 1988;24:574-576.

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    Miller R.L., James-Kracke M., Sun G.Y., Sun A.Y. Oxidative and inflammatory pathways in Parkinson’s disease. Neurochem. Res. 2009;34:55-65.

    Not in our library10.1007/s11064-008-9656-2

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    Hamaguchi T., Ono K., Murase A., Yamada M. Phenolic compounds prevent Alzheimer’s pathology through different effects on the amyloid-beta aggregation pathway. Am. J. Pathol. 2009;175:2557-2565.

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    Smith A., Giunta B., Bickford P.C., Fountain M., Tan J., Shytle R.D. Nanolipidic particles improve the bioavailability and alpha-secretase inducing ability of epigallocatechin-3-gallate (EGCG) for the treatment of Alzheimer’s disease. Int. J. Pharm. 2010;389:207-212.

    Not in our library10.1016/j.ijpharm.2010.01.012

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    Janle M.E., Lila M.A., Grannan M., Wood L., Higgins A., Yousef G.G., Rogers R.B., Kim H., Jackson G.S., Ho L., et al. Pharmacokinetics and tissue distribution of 14C-labeled grape polyphenols in the periphery and the central nervous system following oral administration. J. Med. Food. 2010;13:926-933.

    Not in our library10.1089/jmf.2009.0157

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    Stevenson D.E., Hurst R.D. Polyphenolic phytochemicals—Just antioxidants or much more? Cell Mol. Life Sci. 2007;64:2900-2916.

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    Fraga C.G. Plant polyphenols: How to translate their in vitro antioxidant actions to in vivo conditions. Life. 2007;59:308-315.

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    Karpinar D.P., Balija M.B., Kügler S., Opazo F., Rezaei-Ghaleh N., Wender N., Kim H.Y., Taschenberger G., Falkenburger B.H., Heise H., et al. Pre-fibrillar alpha-synuclein variants with impaired beta-structure increase neurotoxicity in Parkinson’s disease models. EMBO J. 2009;28:3256-3268.

    Not in our library10.1038/emboj.2009.257

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    Marques O., Outeiro T.F. Alpha-synuclein: From secretion to dysfunction and death. Cell Death Dis. 2012;3:e350.

    Not in our library10.1038/cddis.2012.94

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    Masuda M., Suzuki N., Taniguchi S., Oikawa T., Nonaka T., Iwatsubo T., Hisanaga S., Goedert M., Hasegawa M. Small molecule inhibitors of alpha-synuclein filament assembly. Biochemistry. 2006;45:6085-6094.

    Not in our library10.1021/bi0600749

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    Meng X., Munishkina L.A., Fink A.L., Uversky V.N. Effects of various flavonoids on the alpha-synuclein fibrillation process. Parkinsons Dis. 2010;650794:1-16.

    Not in our library10.4061/2010/650794

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    Ehrnhoefer D.E., Bieschke J., Boeddrich A., Herbst M., Masino L., Lurz R., Engemann S., Pastore A., Wanker E.E. EGCG redirects amyloidogenic polypeptides into unstructured, off-pathway oligomers. Nat. Struct. Mol. Biol. 2008;15:558-566.

    Not in our library10.1038/nsmb.1437

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    Bae S.Y., Kim S., Hwang H., Kim H.K., Yoon H.C., Kim J.H., Lee S., Kim T.D. Amyloid formation and disaggregation of alpha-synuclein and its tandem repeat (alpha-TR). Biochem. Biophys. Res. Commun. 2010;400:531-536.

    Not in our library10.1016/j.bbrc.2010.08.088

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    Bieschke J., Russ J., Friedrich R.P., Ehrnhoefer D.E., Wobst H., Neugebauer K., Wanker E.E. EGCG remodels mature alpha-synuclein and amyloid-beta fibrils and reduces cellular toxicity. Proc. Natl. Acad. Sci. USA. 2010;107:7710-7715.

    Not in our library10.1073/pnas.0910723107

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    Lu H., Meng X., Yang C.S. Enzymology of methylation of tea catechins and inhibition of catechol-O-methyltransferase by (−)-epigallocatechin gallate. Drug Metab. Dispos. 2003;31:572-579.

    Not in our library10.1124/dmd.31.5.572

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    Levites Y., Weinreb O., Maor G., Youdim M.B.H., Mandel S. Green tea polyphenol (-)-epigallocatechin-3-gallate prevents N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced dopaminergic neurodegeneration. J. Neurochem. 2001;78:1073-1082.

    Not in our library10.1046/j.1471-4159.2001.00490.x

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    Mandel S., Maor G., Youdim M.B.H. Iron and alpha synuclein in the substantia nigra of MPTP-treated mice: Effect of neuroprotective drugs R-apomorphine and green tea polyphenol epigallocatechin-3-gallate. J. Mol. Neurosci. 2004;24:401-416.

    Not in our library10.1385/jmn:24:3:401

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    Chaturvedi R.K., Shukla S., Seth K., Chauhan S., Sinha C., Shukla Y., Agrawal A.K. Neuroprotective and neurorescue effect of black tea extract in 6-hydroxydopamine-lesioned rat model of Parkinson’s disease. Neurobiol. Dis. 2006;22:421-434.

    Not in our library10.1016/j.nbd.2005.12.008

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    Checkoway H., Powers K., Smith-Weller T., Franklin G.M., Longstreth W.T., Swanson P.D. Parkinson’s disease risks associated with cigarette smoking, alcohol consumption, and caffeine intake. Am. J. Epidemiol. 2002;155:732-738.

    Not in our library10.1093/aje/155.8.732

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    Gao X., Cassidy A., Schwarzschild M.A., Rimm E.B., Ascherio A. Habitual intake of dietary flavonoids and risk of Parkinson disease. Neurology. 2012;78:1138-1145.

    Not in our library10.1212/wnl.0b013e31824f7fc4

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    Baptista F.I., Henriques A.G., Silva A.M.S., Wiltfang J., da Cruz a Silva O.A.B. Flavonoids as therapeutic compounds targeting key proteins involved in Alzehimer’s disease. ACS Chem. Neurosci. 2014;5:83-92.

    Not in our library10.1021/cn400213r

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    Van Cauwenberghe C., Van Broeckhoven C., Sleegers K. The genetic landscape of Alzheimer disease: Clinical implications and perspectives. Genet. Med. 2015;18:421-430.

    Not in our library10.1038/gim.2015.117

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    Contestabile A. The history of the cholinergic hypothesis. Behav. Brain Res. 2011;221:334-340.

    Not in our library10.1016/j.bbr.2009.12.044

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    Cervellati C., Wood P.L., Romani A., Valacchi G., Squerzanti M., Sanz J.M., Ortolani B., Zuliani G. Oxidative challenge in Alzheimer’s disease: State of knowledge and future needs. J. Investig. Med. 2016;64:21-32.

    Not in our library10.1136/jim-2015-000017

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    Folch J., Patraca I., Martínez N., Pedrós I., Petrov D., Ettcheto M., Abad S., Marin M., Beas-Zarate C., Camins A. The role of leptin in the sporadic form of Alzheimer’s disease. Interactions with the adipokines amylin, ghrelin and the pituitary hormone prolactin. Life Sci. 2015;140:19-28.

    Not in our library10.1016/j.lfs.2015.05.002

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    Talbot K., Wang H.Y., Kazi H., Han L.Y., Bakshi K.P., Stucky A., Fuino R.L., Kawaguchi K.R., Samoyedny A.J., Wilson R.S., et al. Demonstrated brain insulin resistance in Alzheimer’s disease patients is associated with IGF-1 resistance, IRS-1 dysregulation, and cognitive decline. J. Clin. Investig. 2012;122:1316-1338.

    Not in our library10.1172/jci59903

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    Commenges D., Scotet V., Renaud S., Jacqmin-Gadda H., Barberger-Gateau P., Dartigues J.F. Intake of flavonoids and risk of dementia. J. Epidemiol. 2000;16:357-363.

    Not in our library10.1023/a:1007614613771

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    Le Bars P.L., Kieser M., Itil K.Z. A 26-week analysis of a double-blind, placebo-controlled trial of the ginkgo biloba extract EGb 761 in dementia. Dement. Geriatr. Cognit. Disord. 2000;11:230-237.

    Not in our library10.1159/000017242

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    Youdim K.A., Joseph J.A. A possible emerging role of phytochemicals in improving age-related neurological dysfunctions: A multiplicity of effects. Free Radic. Biol. Med. 2001;30:583-594.

    Not in our library10.1016/s0891-5849(00)00510-4

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    Joseph J.A., Denisova N.A., Arendash G., Gordon M., Diamond D., Shukitt-Hale B., Morgan D. Blueberry supplementation enhances signaling and prevents behavioral deficits in an Alzheimer disease model. Nat. Neurosci. 2003;6:153-162.

    Not in our library10.1080/1028415031000111282

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    Levites Y., Amit T., Mandel S., Youdim M.B.H. Neuroprotection and neurorescue against amyloid beta toxicity and PKC-dependent release of non-amyloidogenic soluble precursor protein by green tea polyphenol (-)-epigallocatechin-3-gallate. FASEB J. 2003;17:952-954.

    Not in our library10.1096/fj.02-0881fje

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    Ono K., Yoshiike Y., Takashima A., Hasegawa K., Naiki H., Yamada M. Potent anti-amyloidogenic and fibril-destabilizing effects of polyphenols in vitro: Implications for the prevention and therapeutics of Alzheimer’s disease. J. Neurochem. 2003;87:172-181.

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    Morris M.S. Homocysteine and Alzheimer’s disease. Lancet. Neurol. 2003;7:425-428.

    Not in our library10.1016/s1474-4422(03)00438-1

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    Wojtunik-Kulesza K.A., Oniszczuk A., Oniszczuk T., Waksmundzka-Hajnos M. The influence of common free radicals and antioxidants on development of Alzheimer’s Disease. Biomed. Pharmacother. 2016;78:39-45.

    Not in our library10.1016/j.biopha.2015.12.024

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    Dai Q., Borenstein A.R., Wu Y., Jackson J.C., Larson E.B. Fruit and vegetable juices and Alzheimer’s disease: The Kame Project. Am. J. Med. 2006;119:751-759.

    Not in our library10.1016/j.amjmed.2006.03.045

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    Wang J., Zhao Z., Ho L., Seror I., Humala N., Percival S. Moderate consumption of Cabernet Sauvignon attenuates β-amyloid neuropathology in a mouse model of Alzheimer’s disease. FASEB J. 2006;20:2313-2320.

    Not in our library10.1096/fj.06-6281com

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    Luchsinger J.A., Tang M.-X., Siddiqui M., Shea S., Mayeux R. Alcohol intake and risk of dementia. J. Am. Geriatr. Soc. 2004;52:540-546.

    Not in our library10.1111/j.1532-5415.2004.52159.x

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