Starch is composed of amylose, which is a linear α-1,4-linked glucose polymer, and highly branched amylopectin consisting of linear α-1,4-linked glucose chains with α-1,6-linked branch chains. Salivary and pancreatic α-amylases catalyze the endo-hydrolysis of α-1,4-glucosidic linkages releasing mainly maltose, maltotriose and related α-1,6-oligomers. Further digestion takes place in the small intestinal brush border by α-glucosidases, which hydrolyze the terminal α-1,4-linked glucose residues as the final step in the digestion of dietary carbohydrates to release glucose. The α-glucosidase activities, first described as maltases, are associated with maltase-glucoamylase and sucrase-isomaltase [28–30]. In addition to α-1,4-glucosidic activity, sucrase-isomaltase displays specific activities against the α-1,2 linkages of sucrose and α-1,6 linkages of isomaltose.

A variety of polyphenols have been shown to inhibit α-amylase and α-glucosidase activities in vitro (Table 1). The inhibitory polyphenols include flavonoids (anthocyanins, catechins, flavanones, flavonols, flavones and isoflavones), phenolic acids and tannins (proanthocyanidins and ellagitannins). In addition, in vitro inhibitory activities have been reported for polyphenolic extracts of foods, including berries (strawberries, raspberries, blueberries and blackcurrants), vegetables (pumpkin, beans, maize and eggplant), colored grains such as black rice, green and black tea, and red wine (Table 2). In the studies, maltose, sucrose or p-nitrophenyl-α-d-glucopyranoside have been used as substrate for α-glucosidase activity.

Intestinal absorption of glucose is mediated by active transport via the sodium-dependent glucose transporter SGLT1 and by facilitated sodium-independent transport via the glucose transporter GLUT2 [31,32]. On the luminal side of the intestinal brush border membrane, two Na⁺ ions bind to SGLT1 and produce a conformational change that permits glucose binding, followed by another conformational change to allow glucose and Na⁺ to enter the enterocyte. Glucose is released from the enterocyte via GLUT2, a high capacity facilitative transporter in the basolateral membrane, to enter the circulation.

The influence of polyphenols on glucose transporters has been studied in vitro by using intestinal brush border membrane vesicles or everted sacs and Caco-2 cells. Several flavonoids and phenolic acids have been shown to inhibit glucose transport (Table 2). The Na⁺-dependent SGLT1-mediated glucose transport was inhibited by chlorogenic, ferulic, caffeic and tannic acids [33], quercetin monoglucosides [34], tea catechins [35–37] and naringenin [38]. The glucose transport by GLUT2 was inhibited by quercetin, myricetin, apigenin and tea catechins [37,39].

Effects of polyphenols, polyphenolic food fractions, and foods and beverages rich in polyphenols on postprandial blood glucose responses have been investigated in animal models and in human studies. Either glucose, maltose, sucrose, starch or various meals have been used as the carbohydrate challenge.

Animal studies. Diacylated anthocyanin as well as an anthocyanin extract from purple sweet potato reduced the blood glucose and insulin responses to maltose administration in rats [40]. The lack of effect after sucrose or glucose administration indicates that the anti-hyperglycemic effect was achieved by maltase inhibition, and not by inhibition of intestinal sucrase activity or glucose transport. Also a tea polyphenol, theaflavin 3-O-gallate, was effective in suppressing the postprandial glucose response to maltose [41].

A crude Acerola polyphenol fraction (containing anthocyanins) significantly reduced the plasma glucose level after administration of maltose or glucose in mice, suggesting inhibition of α-glucosidase and intestinal glucose transport [42]. A leaf extract of Nerium indicum, a plant used as a folk remedy for type 2 diabetes in Pakistan, was found to reduce the postprandial rise in blood glucose in maltose-or sucrose-loaded rats [43]. A similar response was obtained with chlorogenic acid, which was identified as the major α-glucosidase inhibitor in the leaf extract.

Gingko biloba extracts and their flavonoid fraction reduced the elevation of rat plasma glucose level after oral administration of starch, maltose, sucrose or glucose [44]. Also in diabetic rats, the flavonoid fraction attenuated the glucose response to sucrose and glucose administration. When diabetic rats were administered glucose with quercetin, hyperglycemia was significantly decreased compared to administration of glucose alone [39].

Human studies. Apple juice contains polyphenols such as chlorogenic acid and phloridzin, with higher levels in cloudy juice compared to clear juice. When nine healthy subjects consumed a 25 g glucose load in 400 mL of commercial apple juices, the mean plasma glucose concentrations were significantly lower at 15 and 30 min after ingestion of clear apple juice, and significantly lower at 15 min but significantly higher at 45 and 60 min after ingestion of cloudy apple juice compared to control drink [45]. The effects of apple juices on plasma glucose, insulin, GIP and GLP-1 concentrations were consistent with delayed absorption of glucose.

Berries are rich sources of polyphenols, especially anthocyanins, flavonols, proanthocyanidins and phenolic acids. In twelve healthy subjects, ingestion of sucrose (35 g) with berries (150 g of purée made of bilberries, blackcurrants, cranberries and strawberries providing nearly 800 mg polyphenols) produced a different postprandial glycemic response compared to the control without berries but with comparable profile of available carbohydrates [46]. The shape of the plasma glucose curve with reduced concentrations in the early phase and a slightly elevated concentration in the later phase indicates delayed response due to berry consumption. Berries also significantly decreased the peak glucose increment. Reduced rates of sucrose digestion and/or absorption from the gastrointestinal tract are the most probable mechanisms underlying the delayed and attenuated glycemic response. In another study, consumption of cranberry juice sweetened with high-fructose corn syrup resulted in different (but not statistically significant) pattern of postprandial glycemia compared to the similar amount of the sweetener in water [47].

In ten type 2 diabetic patients, red wine (200 mL) taken during a midday meal induced a smaller increase in blood glucose versus the same meal accompanied by an equivalent amount of water, with no effect of plasma insulin levels [48]. Comparable results were obtained with tannic acid, a polyphenolic component of red wine. Ethanol had no effect. In ten healthy young adults, sugar cane bioflavonoid extract reduced the postprandial glycemic response to a high-glycemic starchy meal composed of wheat biscuits and milk [49]. Ingestion of cinnamon (6 g) with rice pudding significantly lowered blood glucose response in the postprandial phase (15, 30 and 45 min) in 14 healthy subjects [50,51]. However, in another study of the same group [51], cinnamon (3 g) reduced postprandial serum insulin and increased GLP-1 concentrations without significantly affecting blood glucose response. Cinnamon has high content of proanthocyanidins.

Gastrointestinal hormone (GIP and GLP-1) profiles after consumption of 25 g glucose with coffee (400 mL containing 350 mg chlorogenic acid) indicated delayed intestinal absorption of glucose in nine healthy subjects [52]. The authors concluded that chlorogenic acid, the major polyphenol of coffee, might attenuate the intestinal glucose absorption rates and shift the site of glucose absorption to more distal parts of the intestine. In overweight men, chlorogenic acid (1 g) reduced early glucose and insulin responses during an oral glucose tolerance test [53]. Attenuated glycemic response has also been observed when sucrose (25 g) was consumed in chlorogenic acid enriched instant coffee [54].

When either 250 mL of coffee or tea was consumed with test meals, they increased the overall mean peak blood glucose concentration, but did not significantly affect the incremental area under the glucose response curve of the meals [55]. Coffee and tea contain caffeine, which increases postprandial glycemia and impairs glucose tolerance [52,56,57]. Caffeinated coffee ingested with either a high or low glycemic meal significantly impaired acute blood glucose management and insulin sensitivity compared with ingestion of decaffeinated coffee [57]. Instant black tea consumed with glucose reduced the late phase plasma glucose response with a corresponding increase in insulin [58]. The attenuation of late postprandial glycemia may be explained by an elevated insulin response following stimulation of pancreatic β-cells rather than by retarded absorption of glucose.

In conclusion, the scientific evidence on the potential of polyphenolic compounds to retard carbohydrate digestion and absorption and to suppress hyperglycemia in the postprandial state is promising. However, it is mostly based on simple in vitro and animal studies. Current evidence from human studies suggests that beverages such as apple juice, red wine and decaffeinated coffee as well as berries and cinnamon may improve short-term glycemic control. For substantiation of the benefits of polyphenols in the control of postprandial glucose homeostasis, more clinical studies involving subjects with normal and impaired glucose metabolism are needed. These studies should be focused on the effects of dietary polyphenols on glycemic responses induced by starch and sucrose, the main high-glycemic carbohydrates in our diet.

There are few recent studies where soy isoflavonoids at physically achievable concentrations have shown positive impact on β-cell function. Choi et al. [62] used genistein and daidzedin in order to study factors related to glucose and insulin metabolism using a non-obese diabetic mouse model which spontaneously develops autoimmune insulin dependent diabetes mellitus. Both isoflavonoids (0.2 g/kg genistein or daidzein for nine weeks) preserved the insulin production by the β-cells, whereas mice fed the control diet had no insulin production [62]. Another in vivo study performed in non-obese mice (streptozotocin (STZ) induced diabetic model) fed with fermented soybean, a Korean food ‘chungkukjang’ (5 g/100 g of diet for 6 weeks), similarly showed that the insulin concentration in pancreas was higher in the soybean- fed mice than in the non-treated control mice. In addition to enhancing the insulin production in pancreas the treatment also seemed to contribute to improved insulin sensitivity in peripheral tissues, thus necessitating smaller amounts of insulin and preventing pancreatic exhaustion [63]. The same line in results was obtained also by Lu et al on high-isoflavone soy protein fed STZ-diabetic rats [64].

Epigallocatechin gallate (EGCG) and rutin were examined for their ability to attenuate the glucotoxicity in rat insulinoma pancreatic β-cells (RIN m5F) [65]. The treatment increased glucose dependent insulin secretion, and was able to promote effective secretion of insulin also under chronic high glucose incubation when insulin secretion is suppressed by glucotoxicity (33 mM, 48 h), suggesting that both EGCG and rutin might preserve the glucose- sensing ability during hyperglycemia. EGCG and rutin elevated the intracellular ATP, suggesting that the increase in insulin secretion is mediated by enhancing the normal, glucose induced insulin secretion that is dependent on ATP concentrations. Interestingly, epicatechin, the precursor of EGCG, was found to inhibit insulin secretion when tested on INS-1 cells [66].

A very detailed study on the effects of dietary phenolic acids on pancreas function was carried out with cinnamic acid derivatives in INS-1 cell culture and perfused rat pancreas [67]. Among the differentially substituted cinnamic acid derivatives, the most prominent insulin releasing agents were the ones containing m-hydroxy and p-methoxy residues on the phenol ring structure, whereas cinnamic acid (no substituents in the phenol ring) was inactive. The structure promoting insulin secretion most effectively was the one of ferulic acid, containing p-hydroxy and m-methoxy structure, as it enhanced insulin secretion in a dose-dependent manner (1–100 μM), being significant already at 1 μM concentrations. Notably, the assays were performed in absence of glucose, whereas the majority of other reports have focused on glucose dependent insulin release. The results were verified also with treatment of perfused rat pancreas and intravenous administration in normal rats, where the increase in plasma insulin was detected in fasting state. Interestingly, isoferulic acid, the stereoisomer of ferulic acid did not have any effect on insulin releasing properties. This finding corroborated earlier results showing that plasma glucose lowering properties of isoferulic acid are due to increase in glucose uptake and retarding of hepatic gluconeogenesis, without any effect on pancreatic insulin output [68]

In one of the most recent studies isoflavonoids were shown to improve glucose stimulated insulin secretion in INS-1E pancreatic cell line but this effect was not due to modulation of insulin synthesis, since there was no difference on the insulin concentration in the genistein treated and non-treated cells. However, the insulin secretion upon glucose stimulation was significantly increased after 48h pre-treatment with genistein (1–5 μM). It was suggested that the effect of genistein on promoting glucose dependent insulin secretion was not mediated by the same mechanism as glucose stimulation alone, since several cellular factors related to glucose-induced insulin secretion, e.g., cellular ATP concentration, were not changed. The finding that cellular Ca²⁺ levels were elevated by the genistein treatment suggests that the improvement in insulin secretory function may be attributable to modulation of Ca²⁺ signaling and cAMP/protein kinase A (AMPK) function, but the mechanism is not yet clear [69]. The effect of genistein on insulin secretion was observable also in mouse and human pancreatic islets showing non-species-specific and biologically relevant effect.

Also numerous other publications report on the insulin secretagogic activities of dietary phenolics e.g., anthocyanidin and anthocyanin compounds in INS-1 cell line [70], aspalathin, component from rooibos tea Aspalathus linearis, in RIN-5F cells [71], and compounds isolated from Eriobotrya japonica in INS-1 Cells [66].

There are also indications for the function of polyphenols on β-cells by other mechanisms besides affecting insulin secretion. Ethanol extracts from the root, stem, leaf and fruit of the Canadian lowbush blueberry Vaccinium angustifolium, a very rich source of flavonoids, were analyzed for insulin secretagogue and proliferative effects [72]. The insulin secretion was measured from growth arrested (tetracycline-treated) β-cells in order to distinguish the insulinotropic effect from the cell proliferative effect. Only slight enhancement was observed in the glucose stimulated insulin secretion with the treatment by leaf and stem extracts, but the effect on the cell proliferation rate was found to be significantly increased by the treatment with the fruit extract when compared to vehicle-only control, suggesting a potential capability to restrain β-cell damage in metabolic syndrome.

Another study showing β-cell protective effect of flavonoids was performed by mixtures of flavonoids quercetin, luteolin and apigenin in RINmF5 cells [73]. Flavonoids showed anti-inflammatory action in a treatment with interleukin 1β (IL-1β) and interferon γ (IFN- γ), and the effect was verified at transcriptional analysis of inflammation-related genes, suggesting a role for flavonoids in the restoration of insulin secretion capacity by preventing the cytokine-induced β-cell damage.

Oral administration of rutin (100 mg/kg, 45 days) was shown to promote β-cell viability in STZ induced diabetic rats [74]. It was suggested that the β-cell restoring effect of rutin was due to enhanced ability to scavenge free radicals and mediate antioxidant enzyme activity in the pancreas. Similarily, quercetin, the aglycon molecule of rutin, showed β-cell restoration when used as dietary supplement (0.5% of diet for 14 days) in STZ induced diabetic mice [75]. Gene expression analysis showed that quercetin restored the cell proliferation capacity inhibited by STZ treatment, and resulted in higher plasma insulin levels. In addition oxidative stress markers were reduced in pancreas, further ameliorating the oxidative damage associated with diabetes. Quercetin has been studied also in STZ-diabetic rats by intraperitoneal injection, and the preservation of islet cells and restoration of insulin production has been observed in two studies [76,77].

Intraperitoneal injection of (−)epicatechin in alloxan treated mice demonstrated β-cell- regenerative capacity [78]. Similarily, (−)epicatechin or quercetin promoted increased release of insulin when isolated rat islets were exposed to them, whereas naringenin and chrysin inhibited it [79]. Additional observations with dietary sources of polyphenols include the protection of non-obese diabetic mice pancreatic islets from infiltration of immune cells and induction of insulitis by feeding grape powder and high vitamin A supplement [80]. An interesting approach was taken to study olive mill waste which is a rich source of phenolic compounds, especially phenylethanol compound hydroxytyrosol. Fractions of olive mill waste were studied for a range of hypoglycemic and antioxidative effects, including the effect in insulin secretion in alloxan- induced diabetic rats administered by intraperitonial injection. Mainly the purified hydroxytyrosol fraction showed protective action on alloxan-damaged β-cells [81].

Phytochemical- rich extracts from other than dietary plants have also been studied for their impact on pancreatic insulin production and release. Studies have focused especially on medicinal plants known for their anti-diabetic effects. Seed extracts of Eugenia jambolana enhanced insulin secretion from isolated islets of STZ-induced diabetic rats in the presence of 10 mM glucose [82]; eupatilin, a flavone from Artemisia princes, elevated pancreatic insulin concentration in type 2 diabetic mouse model (db/db) [83]; and aqueous extract from Abutilon indicum, a plant used as traditional medicine in Thailand, stimulated insulin secretion from isolated rat islets and INS-1E cells [84]. A fraction containing apigenin and rutin from Teucrium polium, a medicinal plant from Iran, mediated insulin secretion increase in the presence of STZ on isolated rat pancreatic islets [85].

In conclusion, it is obvious that the pancreas is one of the targets of dietary polyphenol bioactivity, as several of the studied plant extracts and purified compounds exhibit beneficial effects on β-cell function and insulin release in different diabetic models. However, no single mechanism has been identified to be responsible for the response. For instance, in INS-1E cells genistein did not increase the level of intracellular ATP upon the glucose stimulation, whereas treatment of the RIN-m5F cells with EGCG and rutin elevated the ATP level [65]. This suggests that the latter treatment enhanced the signaling route mediated normally by glucose, whereas the genistein treatment had effect on alternative mechanism of insulin secretion. A range of different compounds and plant food extracts studied show various activities relevant for insulin secretion, and the activities are different on normoglycaemic controls and the subjects with symptoms of metabolic syndrome. The different effects of various molecules were highlighted in a study showing that even small changes (e.g., hydroxylation) on the molecular backbone result in different insulin- releasing capacity [67]. The studies have been made mainly using cell cultures and animal models, and motivate to proceed to human controlled trials.

Chlorogenic acid and ferulic acid caused a modest, but significant increase in 2-deoxy-d-glucose transport into L6 myotubes, showing comparable performance to metformin and 2,4-thiazolodinedione, two common commercial oral hypoglycemic drugs [94]. Purified aspalathin from green roiboos extract increased dose-dependently and significantly glucose uptake by L6 myotubes at concentrations 1–100 μM, irrespective of insulin absence [71]. As aspalathin is capable of scavenging intracellular reactive oxygen species (ROS), its antioxidative function may be involved in the stimulation of glucose uptake and insulin secretion, and hence glucose homeostasis. An inhibitory effect of EGCG was observed in L6 skeletal muscle cells on insulin resistance induced by dexamethasone, a glucocorticoid [95]. A 24 h- treatment with EGCG attenuated the effect of dexamethasone on glucose uptake and improved insulin-stimulated glucose uptake in a dose-dependent manner by increasing GLUT4 translocation to plasma membrane [95]. EGCG was able to increase the phosphorylation of AMPK, suggesting that the AMPK signalling pathway is likely responsible for the EGCG-stimulated GLUT4 translocation.

Resveratrol increased glucose uptake in C2C12 skeletal muscle cells by activating AMPK [96]. In the absence of insulin, the effect of resveratrol on glucose uptake was primarily dependent on AMPK activation, without involving PI3K. In the presence of insulin, resveratrol also potentiated the effect of insulin on glucose uptake via AMPK activation, but leading to activation of the PI3K-Akt signal pathway [96]. Resveratrol treatment during 15 weeks increased both insulin-stimulated whole-body and steady-state glucose uptake of both soleus muscle and liver in high cholesterol-fructose-fed rats [97]. It enhanced membrane trafficking activity of GLUT4 and increased phosphorylation of IR in insulin-resistant soleus muscles. Interestingly the activation of estrogen receptor seems to be crucial for resveratrol-stimulating muscular glucose uptake via both insulin-dependent and –independent pathways [97]. Additional putative function for resveratrol was found in a study reporting that Akt/protein kinases B (PKB) and GLUT4 or GLUT1 translocation is not involved in resveratrol activation. The mechanism seems to involve sirtuin-dependent AMPK activation that may lead to stimulation of the intrinsic activity of GLUT4 [98]. Sirtuins are a family of histone/protein deacetylases, among which, SIRT1 has been suggested to play a role in regulating glucose homeostasis and may be involved in the insulin signalling cascade [99,100].

Kaempferol and quercetin isolated from the traditional Chinese medicine Euonymus alatus improved glucose uptake of insulin stimulated 3T3-L1 mature adipocytes and had no effects on GU without insulin [101]. The results indicated that both flavonoids could ameliorate insulin resistance peripherally, similar to a PPARγ agonist such as rosiglitazone. Kaempferol 3-neohesperidoside, a flavonoid glycoside isolated from Cyathea phalerata, stimulated glucose uptake in rat soleus muscle mainly via the PI3K pathway [102]. Another kaempferol derivative, kaempferitrin (3,7-dirhamnoside), has recently been shown to inhibit GLUT4 mediated glucose uptake in differentiated 3T3-L1 cells by interfering with insulin signaling pathway and also by directly interacting with membrane GLUT4 [103]. Contradictory, at the same time other authors have found opposite results for kaempferitrin treatment of the same cell line, demonstrating increase in the glucose uptake [104]. The latter results agreed with the glucose uptake stimulation by kaempferitrin found in rat soleus muscle [105]. This suggests that the effect of kaempferitrin on insulin mediated glucose uptake might be a cell type specific function. Inhibitory effect on glucose uptake has been observed in adypocyte cells also by the isoflavone genistein with concentrations 20–50 μM [106].

Several plant based foods and extracts have been reported to enhance glucose uptake in vitro. A green tea polyphenolic extract was reported to regulate the expression of genes involved in glucose uptake and insulin signalling pathways in the muscle tissue from rats with metabolic syndrome induced by a high fructose diet [107]. The tea extract significantly increased the mRNA levels of GLUT4 in the muscle. A procyanidin extract from grape seed has been reported as an insulinomimetic agent since it stimulates glucose uptake in 3T3-L1 adipocytes and L6E9 muscle cells via PI3K – pathway [108]. A more detailed study with same approach showed recently that the grape seed extract interacts with the insulin receptor inducing its phosphorylation and consequently leading to increased glucose uptake via pathway requiring Akt. However, the treatment leads to differential phosphorylation of the insulin signalling pathway proteins than insulin does [109].

Fruit juice extract of Momordica charantia (bitter melon) was shown to stimulate glucose and amino acid uptakes into L6 muscle cells in a similar manner to insulin [110]. Pharmacological concentrations had inhibitory effects, while physiological concentrations had insulin-like stimulating effects, a finding that points out the importance of the concentration of the bioactive compounds in stimulating glucose uptake into muscle cells. Water-soluble components in bitter melon also enhanced the glucose uptake at sub-optimal concentrations of insulin in 3T3-L1 adipocytes, which was accompanied by an increase in adiponectin secretion [111]. Charantin, steroid, glycosides, flavonoids and their derivatives may in part be responsible for the observed up-regulatory activities of glucose uptake and mRNA expression of GLUT4, PI3K and PPARγ in bitter melon extracts but more research is needed to confirm this statement [112]. Another study on the effect of fruit juices on the glucose uptake was performed with blueberry juice. The biotransformation of the juice with a novel strain of bacteria isolated from the blueberry flora (Serratia vaccinii) increased its phenolic content and antioxidant activity [113] and modified its biological activity [72]. The juice extract increased AMPK phosphorylation and glucose uptake in both muscle cells and adipocytes, but it also inhibited adipogenesis [114].

Common spices, such as cinnamon, cloves, turmeric and bay leaves also show insulin-like activity in vitro [115]. For instance, cinnamon polyphenols with doubly linked procyanidin type-A polymers appear to be unique for their insulin- like activity [115]. A water-soluble cinnamon extract showed to increase the activity of autophosphorylation of the IR and decrease the activity of tyrosine phosphatase in vitro [116]. The mechanism of cinnamon’s insulin-like activity may be in part due to increases in the amounts of IRβ and GLUT4 [117]. In vivo insulin-regulated glucose utilization was also enhanced by cinnamon extracts by increasing glucose uptake in rats with insulin resistance induced by a high-fructose diet [118,119].

Several plant extracts from plants used in traditional medicine have been as well reported to promote insulinotropic / insulinomimetic activities. Four isoflavonoids (genistein-derivatives), recently identified from a branch extract fraction of the Vietnamese traditional herb Tetracera scandens, exhibited significant glucose uptake activity both in basal and insulin-stimulated skeletal muscle cells in a dose-dependent manner. AMPK activation and GLUT4 and GLUT1 expressions appear to be involved in the glucose uptake stimulation mechanism [120]. A recent review has also reported that penta-galloyl-glucose (PGG), a polyphenolic compound highly enriched in a number of medicinal herbals, exhibits multiple biological activities relevant in diabetes prevention [95]. Both β-PGG and its anomer α-PGG have showed insulin-mimicking activity in the absence of insulin, and α-PGG was more potent than β-PGG [121]. α-PGG itself stimulated glucose uptake in 3T3-L1 adipocytes. However, α-PGG weakened the activity of insulin if treated together. α-PGG induced phosphorylation of the IR, PI3K and Akt, and stimulated membrane translocation of GLUT4. Plant root extracts can also exert glucose uptake enhancement properties. For example, the aqueous extract of Canna indica root (Cannaceae), rich in flavonoid compounds, caused a dose- and time- dependent induction of glucose uptake activity in L8 muscle cells [122]. The authors suggested that GLUT1 protein synthesis and the activation of PI3K are critical for the increase in glucose transporter activity at the plasma membrane.

In conclusion, insulin stimulates glucose uptake in skeletal muscle and adipose tissue primarily by eliciting the translocation of GLUT4 from an intracellular pool to the plasma membrane [123]. Current data suggest that polyphenols mainly affect glucose transport and insulin-receptor function, both of which play essential roles in diseases related to carbohydrate metabolism [124]. To date glucose uptake data from polyphenols mainly derives from animal cell culture studies. The most likely mechanism implies the PI3K activity signaling route. Recent studies use amounts of phenolic compounds closer to physiological range. However, doses of relevance to human health are still unknown, and deserve further research.

Tea catechins and their effects on liver glucose metabolism have been effectively studied in animal and cell culture models. Green tea extracts and green tea catechins such as epigallocatechin alone have been shown to decrease blood glucose levels and concomitantly also liver triglyceride contents. In streptozotocin-induced diabetic rats oral administration of EGCG (25 mg/kg b.w./day) for eight weeks significantly alleviated the increase in serum glucose levels and serum TG levels [132]. However, the study did not include any tissue specific analyses. Supplementation of the diet with 0.5% and 1.0% green tea for six weeks reduced liver TG concentrations 27–30% in fructose-fed ovariextomized rats as compared to fructose and starch fed control diets [133]. Several other studies have also shown reduced blood glucose levels and liver TG contents after feeding with green tea or EGCG. For instance, supplementation of high-fat diet (60% energy as fat) fed mice with dietary EGCG (3.2 g/kg diet) for 16 weeks resulted in decreased blood glucose levels and decreased liver TG contents [134].

The potential mechanisms explaining how liver could contribute to the reduced blood glucose levels in green tea and EGCG treated animal models have been studied as well. Wolfram et al. [135] assessed glucose and insulin tolerance in db/db mice and investigated the effect of 5–7 weeks EGCG supplementation on gene expression in liver tissue using real-time quantitative PCR (RT-PCR). EGCG supplementation (2.5–10.0 g/kg) resulted in decreased blood glucose levels in a dose dependent manner as tested by OGTT. In the fed state plasma glucose, free fatty acid and TG levels were lower and insulin levels higher in EGCG-treated db/db mice than in control mice. EGCG treatment increased the expression of liver glucokinase (glycogenic enzyme), carnitine palmitoyl transferase-1β and decreased the expression of gluconeogenetic enzymes phosphoenolpyruvate carboxykinase (PEPCK). The authors suggested that the potential mechanisms to explain the T2DM amelioration by the dietary supplementation of EGCG could be the reduced endogenous liver glucose production and increase in glucose-induced insulin secretion [135]. Furthermore, DNA microarray analysis of H4IIE rat hepatoma cells exposed to EGCG (50μM), showed that genes involved in the synthesis of fatty acids, triacylglycerol, and cholesterol were strongly downregulated, also genes involved in gluconeogenesis were downregulated whereas genes involved in glycogenesis were upregulated.

These findings are in line with cell culture studies that have shown reduced hepatic gluconeogenesis and glucose output after exposure to EGCG or green tea extract [136,137]. For instance, Collins et al. [136,137] studied the role of EGCG in hepatic gluconeogenesis using isolated hepatocytes exposed to physiologically relevant concentrations of EGCG (≤1 μM). EGCG decreased glucose production by inhibiting expression of the gluconeogenetic enzymes (PEPCK and glucose-6-phosphatase) in a similar manner to insulin. However, EGCG was not found to activate the insulin signalling pathway. Further tests showed that EGCG activated AMPK, which was shown to be necessary for the observed inhibition of gluconeogenetic enzyme expression. AMPK activation was mediated by the calmodulin-dependent protein kinase kinase CaMKK [136]. Furthermore, ROS production induced by EGCG was shown to be required for the activation of AMPK and inhibition of gluconeogenesis. The study by Collins et al. showed that EGCG exerts toxic effects on primary hepatocytes already at concentration of 10 μM. Other studies have found EGCG to have similar effects on hepatic glucose metabolism, though with concentrations exceeding 10 μM [137,138].

Similarly to green tea also soy and soy isoflavones genistein and daidzein supplementation (0.2 g/kg) have been found to decrease blood glucose levels and to reduce liver TG concentrations in db/db mice model [139] and in non-obese diabetic mice [62]. Both studies found reduced glucose-6-phosphatase and PEPCK liver activities and increased glucokinase activities suggesting that genistein and daidzein suppresses liver glucose output. Cederroth et al. [140] studied the mechanisms behind the effects of soy supplementation rich in equol, daidzein and genistein, in normal CD-1 mice. Phytoestrogen- rich supplementation (198 ppm daidzein and 286 ppm genistein equivalents in the high phytoestrogen diet) from conception to adulthood was found to activate AMPK in liver but also in white adipose tissue and muscle. The authors hypothesised that high-phytoestrogen-fed mice would have altered mitochondrial metabolism and found that the expression of peroxisome proliferator-activated receptor α (PPARα) and its coactivator peroxisome proliferator-activated receptor γ coactivator (PGC-1α) were upregulated in liver, white adipose tissue and muscle suggesting improved fatty acid β-oxidation [140]. Potentially, in normal (non-obese) mice activation of PPARα could lead to change from glucose utilization to fatty acid oxidation to produce fuels, instead of creating new TGs [141]. Increased fatty acid β-oxidation might protect against non-alcoholic hepatic steatosis and therefore could also improve insulin sensitivity and glucose metabolism in liver. Furthermore, decrease in hepatic TG pools has been shown to correlate with improved insulin sensitivity [130]. However, the role of TGs in the development of insulin resistance is not yet clear. Chungkukjang (a fermented soybean food) supplementation also resulted in significantly higher hepatic GK activity and decreased activity of gluconeogenic enzymes G6Pase and PEPCK in db/db mice when compared to control group [142]. However, also insulin secretion was improved after Chungkukjang supplementation.

The citrus flavonoids, hesperidin and naringin (0.2 g/kg) were shown to lower blood glucose levels as compared to the control diet fed to db/db mice [143]. Similarly to green tea and soy, hesperidin and naringin also significantly reduced plasma free fatty acid, TG and total cholesterol levels in plasma as well as hepatic TG content. These physiological changes were postulated to be due to increase in hepatic glucokinase mRNA, decrease in expression of the gluconeogenetic enzymes PEPCK and G6Pase, and improvement in lipid metabolism caused by altered activities of hepatic lipid metabolizing enzymes [143,144]. Furthermore, naringenin (25–100 μM), the aglycone form of naringin, was shown to suppress hepatic glucose production from hepatoma cells in a dose dependent manner even though naringenin did not have any impact on gluconeogenetic gene expression [145]. However, naringenin exposure led to decrease in cellular ATP levels.

Grape seed-derived polyphenols such as procyanidins have been also shown to alleviate insulin resistance in mice fed with high-fat diet. Simultaneous supplementation of grape-seed derived procyanidin-rich extract and G. pentaphyllum extract (altogether 80 mg/kg) improved glucose tolerance and HOMA-IR index, as well as lowered the high-fat-diet induced serum glucose levels and also increased the activity of hepatic glucokinase [95].

Unlike polyphenols discussed above, resveratrol was shown to have opposite effects and increase the expression and activity of gluconeogenetic enzymes. As Ganjam et al. [146] showed, rats treated with resveratrol (5–10 mg/kg/day) by intraperitoneal injections for 2 days lead to decreased GK mRNA levels in liver in a dose-dependent manner. The decreased GK mRNA expression was accompanied by a reduction in GK protein levels. In primary rat hepatocyte cultures resveratrol (10–50 μM) also suppressed GK expression and conversely enhanced PEPCK expression. The suppression of GK by resveratrol was found to be mediated, at least partly, by the deacetylation of FoxO1-transcription factor and further binding to HNF-4 (hepatocyte nuclear factor) that can restrain it from its binding site in the proximal GK promoter [146]. Similar effects of resveratrol on hepatic glucose metabolism have been shown with H4IIE rat hepatoma cells [147]. However, there are controversial findings showing that activation of SIRT1 was repressing forkhead transcription factors including Foxo1 in different cell models [148]. On the other hand, the results are supported by the fact that knockdown of SIRT1 in liver leads to decrease in gluconeogenesis [149]. The roles of Foxos and sirtuins in the regulation of hepatic glucose metabolism clearly need further clarification.

Administration of phenolic acid fraction of rice bran containing considerable amounts of trans-cinnamic acid derivatives (ferulic acid, and p-coumaric acid) and ferulic acid alone for 17 days was shown to exert hypoglycemic effects and to elevate liver glycogen synthesis and glucokinase activity in db/db mice compared with the control group [150]. Insulin secretion was also improved, and it was postulated that the rice bran fraction and ferulic acid could have increased insulin action and the utilization of dietary glucose in the liver.

In conclusion, several different polyphenol classes have been shown to reduce hepatic glucose output by suppressing gluconeogenetic enzyme expression and increasing the activity of glucokinase to improve glycogenesis and glucose utilization. EGCG has been shown to exhibit these effects by activating AMPK. Furthermore, theaflavins have been shown to activate AMPK in HepG2 cells and to attenuate hepatic lipid accumulation [151]. Activation of AMPK by dietary polyphenols leads to suppression of hepatic gluconeogenesis and induction of fatty acid β-oxidation that both improve hepatic glucose utilization and insulin sensitivity [152]. Resveratrol seems to function in opposite way by activating FoxO1 and inducing hepatic gluconeogenesis. In contrast, resveratrol has been also shown to activate hepatic AMPK [153,154]. Therefore the role of resveratrol in hepatic glucose metabolism needs further clarification. Recent findings suggest that FoxO1 integrates insulin signalling with hepatic mitochondrial function and inhibition of Foxo1 can improve hepatic metabolism during insulin resistance and the metabolic syndrome [155]. In addition to the changes in hepatic glucose utilization and output, most of the in vivo studies report changes in hepatic TG contents as well as in blood TG contents. As the hepatic lipid accumulation is connected to insulin resistance it is therefore possible that phytochemicals could exert their effects indirectly on hepatic glucose output by influencing lipid metabolism. In vivo studies have also reported increased insulin secretion or changes in blood insulin levels after polyphenol rich diet and therefore the hepatic effects could be also due to insulin signalling.

In epidemiological studies, very few of the individual polyphenolic compounds alone have been so far demonstrated to have a beneficial effect on prevention of type 2 diabetes. A prospective study of flavonoid intake from the Finnish diet concluded that quercetin and myricetin are associated with reduced risk of type 2 diabetes [5]. On contrary, intakes of quercetin, kaempferol, myricetin, apigenin, and luteolin were not associated with reduced risk of type 2 diabetes in The Women’s Health Study [156]. However, the inverse association with diabetes risk in epidemiological studies has been shown with whole polyphenol-rich diets/food items, which suggests that the effects of polyphenols on disease risk cannot be attributed to single compounds. This is an important issue for consideration for the mechanistic studies using in vitro models. Whole grain rich diets have been linked with decreased risk of obesity and type 2 diabetes in epidemiological studies [157,158], and high coffee consumption has been associated with lower prevalence of metabolic syndrome [19,159]. Apples and tea consumption have also been linked to lowered incidence of type 2 diabetes in middle-aged women [156], and apples and berries were the most important contributors lowering the risk in Finnish men and women [5]. In a meta-analysis including nine cohort studies with follow-up ranging from 5 to 18 years, tea consumption was associated with prevention of development of type 2 diabetes [160]. Over four cups of tea per day was required to produce the beneficial effect, although also smaller intake has been shown to be effective in lowering the risk of obesity and blood glucose levels [161]. These beneficial effects by both coffee and tea intakes have been demonstrated also in a recent cohort study where the effect of single compounds magnesium, potassium, and caffeine alone was excluded, and it also was concluded that the effect was not mediated by blood pressure lowering effect [162].

There are only a few controlled interventions studying the effects of specific polyphenols or food products in amelioration of the symptoms of the metabolic syndrome. One of the polyphenols studied most frequently in vitro is EGCG and/or its source green tea extract. In spite of promising results from animal and in vitro testing, EGCG treatment has not been shown to improve insulin resistance in humans, although some beneficial health impacts have been observed [163,164]. One study on type 2 diabetes patients showed increased levels of insulin after 12 weeks of diet supplemented with catechin-rich (582.8 mg) green tea [165], and another study revealed correlation between high intake of tea polyphenols and improved insulin levels in type 2 diabetes patients [164]. In contrast to tea, interesting results have been produced in human trials by dark chocolate consumption. Dark chocolate (100 g dark chocolate bar containing approximately 500 mg of polyphenols for 15 days) improved insulin sensitivity along with reducing blood pressure in healthy subjects [166] and similar results were reported with the same treatment on hypertensive subjects [167]. However, consumption of a flavanol-rich cocoa drink (150 mL twice a day, approximately 900 mg flavanols) for 15 days did not improve insulin resistance or blood pressure in individuals with essential hypertension [168]. Grape seed extract given to type 2 diabetic patients for 4 weeks, had positive effect on several inflammatory markers and glycaemia, but did not result in statistically significant changes in HOMA-IR [169]. In regard of whole grain consumption the beneficial health effects may also be, at least partly, due to the polyphenol content of whole grain products, as a polyphenol-rich wheat bread had higher glucose lowering and antioxidative effect than a control wheat bread during a 9-day study period [170]. Other promising plant food candidates with diabetes preventive potential include cinnamon, bitter melon and fenugreek [171].

On the other hand, considerable evidence is available on the effects of several polyphenols and polyphenol-rich food items in ameliorating insulin resistance and improving insulin sensitivity in experimental animals. In mice fed high-fat diet indications towards beneficial effect in glucose/insulin signaling have been obtained by catechin [172], EGCG [134], grape seed procyanidins [173], and blueberry [174]. Similarly in rats fed high-fat diet isoflavones [175], quercetin [176], and blueberry [177] have alleviated the markers of metabolic syndrome. Another type of high-calorie diet, fructose-rich diet, has been applied in rat experiments, producing promising results in balancing the glucose/insulin metabolism with myricetin [178], fenugreek seed extract or quercetin [179], longan flower extract [180], green tea [181] and cinnamon [119,179]. Moreover, insulin sensitivity was improved in the CD-1 mice that have genetic susceptibility to obesity and type 2 diabetes by feeding a diet containing soy [140].

In conclusion, the evidence from epidemiological studies on the protective role of polyphenol-rich foods against development of type 2 diabetes is suggestive, but in spite of the large array of studies in vitro and the positive results in animal models, only a handful of controlled human interventions confirm these results. The discrepancy between the results from animal and human studies may be due to species specific differences, but also other factors such as genetic variability and general study set-up (dosage of supplementation, number of study objects, length of intervention) most likely have an impact on the outcome. It is clear that more tightly controlled human studies should be conducted in order to draw conclusions about the role of polyphenols in insulin resistance.