Abstract
This paper provides an overview of work that suggests that polyphenol components from berries can inhibit crucial enzymes involved in starch and lipid digestion and potentially influence blood glucose levels and fat digestion. Polyphenols from certain berries have been found to inhibit lipase activity in vitro at low levels. By screening berries with differing polyphenol composition for their inhibitory effectiveness, certain polyphenol classes were implicated as active components. The inhibition was caused at low levels, certainly achievable in the gut after intake of a small amount of berries and approached inhibition achieved by the pharmaceutical lipase inhibitor, orlistat. Polyphenols from berries also have the potential to modulate starch digestion as they inhibit both α-amylase activity and α-glucosidase activity in vitro at low levels. Different berries showed very different levels of effectiveness against the two enzymes and a comparison of their polyphenol composition indicated which components were the most effective inhibitors. For α-amylase, tannins (ellagitannins and proanthocyanidins) were found to be the most effective components but their effectiveness may be modulated by other polyphenols. The active components in the inhibition of α-glucosidase were less obvious and a range of different polyphenol classes may be effective. In both cases, the berry components could act additively with the pharmaceutically used inhibitor, acarbose, and there is potential for berry components to substitute for acarbose or reduce the dose required for effective glycaemic control.
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References
Anon (2002) Joint WHO/FAO expert consultation on diet, nutrition and the prevention of chronic diseases WHO Technical Report Series, No. 916, Geneva, Switzerland
Kahkonen M, Hopia A, Heinonen M (2001) Berry phenolics and their antioxidant activity. J Agric Food Chem 49:4076–4082
Halliwell B (1996) Antioxidants in human health and disease. Annu Rev Nutr 16:33–50
Manach C, Scalbert A, Morand C, Rémésy C, Jiménez L (2004) Polyphenols: food sources and bioavailability. Am J Clin Nutr 79:727–747
Kay CD, Kroon PA, Cassidy A (2009) The bioactivity of dietary anthocyanins is likely to be mediated by their degradation products. Mol Nutr Food Res 53:S92–S101
Williamson G, Clifford MN (2010) Colonic metabolites of berry polyphenols: the missing link to biological activity? Br J Nutr 104:S48–S66
McDougall GJ, Shpiro F, Dobson P, Smith P, Blake A, Stewart D (2005) Different polyphenolic components of soft fruits inhibit α-amylase and α-glucosidase. J Agric Food Chem 53:2760–2766
McDougall GJ, Kulkarni NN, Stewart D (2009) Berry polyphenols inhibit pancreatic lipase activity in vitro. Food Chem 115:193–199
Grussu D, Stewart D, McDougall GJ (2011) Berry polyphenols inhibit α-amylase in vitro: identifying active components in rowanberry and raspberry. J Agric Food Chem 59:2324–2331
Whitson J, McDougall GJ, Ross HA, Lund VA, Hamilton CA, Dominiczak AF, Stewart D (2010) Bioactive berry components: potential modulators of health benefits. Funct Plant Sci Biotechnol 4:34–39
Maatta-Riihinen KR, Kamal-Eldin A, Matiila PH, Gonzalez-Paramas AM, Törrönen R (2004) Distribution and contents of phenolic compounds in eighteen Scandinavian berry species. J Agric Food Chem 52:4477–4486
Moreno DA, Ilic N, Poulev A, Brasaemleet D, Fried SK, Raskin I (2003) Inhibitory effects of grape seed extract on lipases. Nutrition 19:876–879
Sugiyama H, Akazome Y, Shoji T, Yamaguchi A, Yasue M, Kanda T, Ohtake Y (2007) Oligomeric procyanidins in apple polyphenol are main active components for inhibition of pancreatic lipase and triglyceride absorption. J Agric Food Chem 55:4604–4609
McDougall GJ, Ross HA, Ikeji M, Stewart D (2008) Berry extracts exert different antiproliferative effects against cervical and colon cancer cells grown in vitro. J Agric Food Chem 56:3016–3023
Kylli P, Nohynek L, Puupponen-Pimiä R, Westerlund-Wikström B, McDougall GJ, Stewart D, Heinonen M (2010) Rowanberry phenolics: compositional analysis and bioactivities. J Agric Food Chem 58:11985–11992
Pinto MD, de Carvalho JE, Lajolo FM, Genovese MI, Shetty K (2010) Evaluation of anti-proliferative, anti-type 2 diabetes, and anti-hypertension potentials of ellagitannins from strawberries (Fragaria x ananassa Duch.) using in vitro models. J Med Food 13:1027–1035
Desseaux V, Kouliekolo R, Moreau Y, Santimone M, Marchis-Mouren G (2002) Mechanism of porcine pancreatic α-amylase: inhibition of amylase and maltopentaose hydrolysis by various inhibitors. Biologia 57:163–170
Akkarachiyasit S, Charoenlertkul P, Yibchok-anun S, Adisakwattana S (2010) Inhibitory activities of cyanidin and its glycosides and synergistic effect with acarbose against intestinal α-glucosidase and pancreatic α-amylase. Int J Mol Sci 11:3387–3396
McDougall GJ, Martinussen I, Stewart D (2008) Towards fruitful metabolomics: high throughput analyses of polyphenol composition in berries using direct infusion mass spectrometry. J Chromatogr B 871:362–369
Slimestad R, Solheim H (2002) Anthocyanins from black currants (Ribes nigrum L.). J Agric Food Chem 50:3228–3231
Li YQ, Zhou FC, Gao F, Bian JS, Shan F (2009) Comparative evaluation of quercetin, isoquercetin and rutin as inhibitors of alpha-glucosidase. J Agric Food Chem 57:11463–11468
Karle K, Kraus M, Scheppach W, Ackermann M, Ridder F, Richling E (2006) Studies on apple and blueberry fruits constituents: do the polyphenols reach the colon after ingestion? Mol Nutr Food Res 50:418–423
Gonzanlez-Barrio R, Borges G, Mullen W, Crozier A (2010) Bioavailability of anthocyanins and ellagitannins following consumption of raspberries by healthy humans and subjects with an ileostomy. J Agric Food Chem 58:3933–3939
Hofmann T, Glabasnia A, Schwarz B, Wisman KN, Gangwer KA, Hagerman AE (2006) Protein binding and astringent taste of a polymeric procyanidin, 1,2,3,4,6-penta-O-galloyl-β-d-glucopyranose, castalagin and grandinin. J Agric Food Chem 54:9503–9509
McDougall GJ, Stewart D (2005) The inhibitory effects of berry extracts on digestive enzymes. Biofactors 23:189–195
McDougall GJ, Kulkarni NN, Stewart D (2008) Current developments on the inhibitory effects of berry polyphenols on digestive enzymes. Biofactors 34:73–80
Pal S, Naissides M, Mamo J (2004) Polyphenolics and fat absorption. Int J Obes 28:324–326
Vadillo M, Ardévol A, Fernández-Larrea J, Pujadas G, Bladé C, Salvadó MJ, Arola L, Blay M (2006) Moderate red wine consumption partially prevents weight gain in rats fed a hyperlipidic diet. J Nutr Biochem 17:139–142
Wolfram S, Wang Y, Thielecke F (2006) Anti-obesity effects of green tea: from bedside to bench. Mol Nutr Food Res 50:176–187
Juhel C, Armand M, Pafumi Y, Rosier C, Vandermander J, Lairon D (2000) Green tea extract (AR25®) inhibit lipolysis of triglycerides in gastric and duodenal medium in vitro. J Nutr Biochem 11:45–51
Hsu C-L, Yen G-C (2007) Phenolic compounds: evidence for inhibitory effects against obesity and their underlying molecular signaling mechanisms. Mol Nutr Food Res 52:53–61
Griffiths DW (1986) The inhibition of digestive enzymes by polyphenolic compounds. Adv Exp Med Biol 199:509–516
Tsuda T (2008) Regulation of adipocyte function by anthocyanins: possibility of preventing the metabolic syndrome. J Agric Food Chem 56:642–646
Takikawa M, Inoue S, Horio F, Tsuda T (2010) Dietary anthocyanin-rich bilberry extract ameliorates hyperglycemia and insulin sensitivity via activation of AMP-activated protein kinase in diabetic mice. J Nutr 140:527–533
Hogan S, Zhang L, Li JR, Sun S, Canning C, Zhou KQ (2010) Antioxidant rich grape pomace extract suppresses postprandial hyperglycemia in diabetic mice by specifically inhibiting alpha-glucosidase. Nutr Metab 7:71–78
Törrönen R, Sarkkinen E, Tapola N, Hautaniemi E, Kilpi K, Niskanen L (2010) Berries modify the postprandial plasma glucose response to sucrose in healthy subjects. Br J Nutr 103:1094–1097
Rosenstock JA, Brown A, Fischer J, Jain A, Littlejohn T, Nadeau D, Sussman T, Taylor A, Krol A, Magner J (1998) Efficacy and safety of acarbose in metformin-treated patients with type 2 diabetes. Diabetes Care 21:2050–2055
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Fig. S1
Effect of bovine serum albumin (BSA) on inhibition of amylase by rowanberry PACs. The values are averages of triplicate assays ± standard error. Two repeat experiments are shown. Rowanberry PACs were added at 4.5 μg GAE/ml and BSA at 100 μg/ml. Control assays without PACs but with BSA were run to assess any protective effect of BSA on amylase activity. Two experiments (1 and 2) are shown. Different letters (a–d) denote significantly different samples at p < 0.05 (Student’s t test). (DOC 40 kb)
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Boath, A.S., Grussu, D., Stewart, D. et al. Berry Polyphenols Inhibit Digestive Enzymes: a Source of Potential Health Benefits?. Food Dig. 3, 1–7 (2012). https://doi.org/10.1007/s13228-012-0022-0
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DOI: https://doi.org/10.1007/s13228-012-0022-0