Possible effects of dietary polyphenols on sugar absorption and digestion
Excessive post‐prandial glucose excursions are a risk factor for developing diabetes, associated with impaired glucose tolerance. One way to limit the excursion is to inhibit the activity of digestive enzymes for glucose production and of the transporters responsible for glucose absorption. Flavonol...
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Veröffentlicht in: | Molecular nutrition & food research 2013-01, Vol.57 (1), p.48-57 |
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description | Excessive post‐prandial glucose excursions are a risk factor for developing diabetes, associated with impaired glucose tolerance. One way to limit the excursion is to inhibit the activity of digestive enzymes for glucose production and of the transporters responsible for glucose absorption. Flavonols, theaflavins, gallate esters, 5‐caffeoylqunic acid and proanthocyanidins inhibit α‐amylase activity. Anthocyanidins and catechin oxidation products, such as theaflavins and theasinsensins, inhibit maltase; sucrase is less strongly inhibited but anthocyanidins seem somewhat effective. Lactase is inhibited by green tea catechins. Once produced in the gut by digestion, glucose is absorbed by SGLT1 and GLUT2 transporters, inhibited by flavonols and flavonol glycosides, phlorizin and green tea catechins. These in vitro data are supported by oral glucose tolerance tests on animals, and by a limited number of human intervention studies on polyphenol‐rich foods. Acarbose is a drug whose mechanism of action is only through inhibition of α‐amylases and α‐glucosidases, and in intervention studies gives a 6% reduction in diabetes risk over 3 years. A lifetime intake of dietary polyphenols, assuming the same mechanism, has therefore a comparable potential to reduce diabetes risk, but more in vivo studies are required to fully test the effect of modulating post‐prandial blood glucose in humans. |
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One way to limit the excursion is to inhibit the activity of digestive enzymes for glucose production and of the transporters responsible for glucose absorption. Flavonols, theaflavins, gallate esters, 5‐caffeoylqunic acid and proanthocyanidins inhibit α‐amylase activity. Anthocyanidins and catechin oxidation products, such as theaflavins and theasinsensins, inhibit maltase; sucrase is less strongly inhibited but anthocyanidins seem somewhat effective. Lactase is inhibited by green tea catechins. Once produced in the gut by digestion, glucose is absorbed by SGLT1 and GLUT2 transporters, inhibited by flavonols and flavonol glycosides, phlorizin and green tea catechins. These in vitro data are supported by oral glucose tolerance tests on animals, and by a limited number of human intervention studies on polyphenol‐rich foods. Acarbose is a drug whose mechanism of action is only through inhibition of α‐amylases and α‐glucosidases, and in intervention studies gives a 6% reduction in diabetes risk over 3 years. A lifetime intake of dietary polyphenols, assuming the same mechanism, has therefore a comparable potential to reduce diabetes risk, but more in vivo studies are required to fully test the effect of modulating post‐prandial blood glucose in humans.</description><identifier>ISSN: 1613-4125</identifier><identifier>EISSN: 1613-4133</identifier><identifier>DOI: 10.1002/mnfr.201200511</identifier><identifier>PMID: 23180627</identifier><language>eng</language><publisher>Weinheim: Blackwell Publishing Ltd</publisher><subject>Absorption ; Acarbose - pharmacology ; alpha-Amylases - antagonists & inhibitors ; alpha-Amylases - metabolism ; alpha-Glucosidases - metabolism ; Amylase ; Animals ; Anthocyanins - pharmacology ; Antioxidants - pharmacology ; Biflavonoids - pharmacology ; Biological and medical sciences ; Carbohydrate Metabolism - drug effects ; Catechin - pharmacology ; Diabetes ; Diabetes Mellitus - prevention & control ; Diabetes. Impaired glucose tolerance ; Diet ; Digestion - drug effects ; Disaccharidases - metabolism ; Disaccharide ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Feeding. Feeding behavior ; Flavonoid ; Flavonols - pharmacology ; Fundamental and applied biological sciences. Psychology ; Glucose - metabolism ; Glucose Tolerance Test ; Glucose transport ; Glucose Transporter Type 2 - genetics ; Glucose Transporter Type 2 - metabolism ; Glycoside Hydrolase Inhibitors ; Humans ; Lactase - antagonists & inhibitors ; Lactase - metabolism ; Medical sciences ; Models, Animal ; Monosaccharides - metabolism ; Plant Extracts - pharmacology ; Polyphenols - pharmacology ; Postprandial Period - drug effects ; Risk Factors ; Sodium-Glucose Transporter 1 - genetics ; Sodium-Glucose Transporter 1 - metabolism ; Sucrase - antagonists & inhibitors ; Sucrase - metabolism ; Tea - chemistry ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>Molecular nutrition & food research, 2013-01, Vol.57 (1), p.48-57</ispartof><rights>2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2014 INIST-CNRS</rights><rights>2012 WILEY-VCH Verlag GmbH & Co. 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Nutr. Food Res</addtitle><description>Excessive post‐prandial glucose excursions are a risk factor for developing diabetes, associated with impaired glucose tolerance. One way to limit the excursion is to inhibit the activity of digestive enzymes for glucose production and of the transporters responsible for glucose absorption. Flavonols, theaflavins, gallate esters, 5‐caffeoylqunic acid and proanthocyanidins inhibit α‐amylase activity. Anthocyanidins and catechin oxidation products, such as theaflavins and theasinsensins, inhibit maltase; sucrase is less strongly inhibited but anthocyanidins seem somewhat effective. Lactase is inhibited by green tea catechins. Once produced in the gut by digestion, glucose is absorbed by SGLT1 and GLUT2 transporters, inhibited by flavonols and flavonol glycosides, phlorizin and green tea catechins. These in vitro data are supported by oral glucose tolerance tests on animals, and by a limited number of human intervention studies on polyphenol‐rich foods. Acarbose is a drug whose mechanism of action is only through inhibition of α‐amylases and α‐glucosidases, and in intervention studies gives a 6% reduction in diabetes risk over 3 years. A lifetime intake of dietary polyphenols, assuming the same mechanism, has therefore a comparable potential to reduce diabetes risk, but more in vivo studies are required to fully test the effect of modulating post‐prandial blood glucose in humans.</description><subject>Absorption</subject><subject>Acarbose - pharmacology</subject><subject>alpha-Amylases - antagonists & inhibitors</subject><subject>alpha-Amylases - metabolism</subject><subject>alpha-Glucosidases - metabolism</subject><subject>Amylase</subject><subject>Animals</subject><subject>Anthocyanins - pharmacology</subject><subject>Antioxidants - pharmacology</subject><subject>Biflavonoids - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Carbohydrate Metabolism - drug effects</subject><subject>Catechin - pharmacology</subject><subject>Diabetes</subject><subject>Diabetes Mellitus - prevention & control</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Diet</subject><subject>Digestion - drug effects</subject><subject>Disaccharidases - metabolism</subject><subject>Disaccharide</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Feeding. Feeding behavior</subject><subject>Flavonoid</subject><subject>Flavonols - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucose - metabolism</subject><subject>Glucose Tolerance Test</subject><subject>Glucose transport</subject><subject>Glucose Transporter Type 2 - genetics</subject><subject>Glucose Transporter Type 2 - metabolism</subject><subject>Glycoside Hydrolase Inhibitors</subject><subject>Humans</subject><subject>Lactase - antagonists & inhibitors</subject><subject>Lactase - metabolism</subject><subject>Medical sciences</subject><subject>Models, Animal</subject><subject>Monosaccharides - metabolism</subject><subject>Plant Extracts - pharmacology</subject><subject>Polyphenols - pharmacology</subject><subject>Postprandial Period - drug effects</subject><subject>Risk Factors</subject><subject>Sodium-Glucose Transporter 1 - genetics</subject><subject>Sodium-Glucose Transporter 1 - metabolism</subject><subject>Sucrase - antagonists & inhibitors</subject><subject>Sucrase - metabolism</subject><subject>Tea - chemistry</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>1613-4125</issn><issn>1613-4133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkElPwzAQhS0EYr9yRLkgcUnxeE2PgGhBKosQqNws27EhkCbBbgX997hqKUdOM_P0vRnNQ-gIcA8wJmeTxocewUAw5gAbaBcE0JwBpZvrnvAdtBfjO8YUCKPbaIdQKLAgchfdPLQxVqZ2mfPe2WnMWp-VlZvqMM-6tp53b65p6yQ3WZy96pBpE9vQTask6KZM7KuLi-kAbXldR3e4qvvoeXD1dHmdj-6HN5fno9wyyUiuKQNuOWNgnJG0MIb1icTSgjacGyxFoTkwKEyZVGMdFZr0nRDeQ8ksp_vodLm3C-3nLN1WkypaV9e6ce0sKiCSEiEYX6C9JWpD-jI4r7pQTdJnCrBaxKcW8al1fMlwvNo9MxNXrvHfvBJwsgJ0tLr2QTe2in-cKArBJU0cW3JfVe3m_5xVt3eDRygKkmz50lbFqfte23T4UEJSydX4bqjGQyFeBv0L9UJ_ANTPlxQ</recordid><startdate>201301</startdate><enddate>201301</enddate><creator>Williamson, Gary</creator><general>Blackwell Publishing Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201301</creationdate><title>Possible effects of dietary polyphenols on sugar absorption and digestion</title><author>Williamson, Gary</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4742-a3415c5441beb738bb492707c1ab55b0768a51418bd707bce36a29e66ff1d4c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Absorption</topic><topic>Acarbose - pharmacology</topic><topic>alpha-Amylases - antagonists & inhibitors</topic><topic>alpha-Amylases - metabolism</topic><topic>alpha-Glucosidases - metabolism</topic><topic>Amylase</topic><topic>Animals</topic><topic>Anthocyanins - pharmacology</topic><topic>Antioxidants - pharmacology</topic><topic>Biflavonoids - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Carbohydrate Metabolism - drug effects</topic><topic>Catechin - pharmacology</topic><topic>Diabetes</topic><topic>Diabetes Mellitus - prevention & control</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Diet</topic><topic>Digestion - drug effects</topic><topic>Disaccharidases - metabolism</topic><topic>Disaccharide</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Feeding. Feeding behavior</topic><topic>Flavonoid</topic><topic>Flavonols - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucose - metabolism</topic><topic>Glucose Tolerance Test</topic><topic>Glucose transport</topic><topic>Glucose Transporter Type 2 - genetics</topic><topic>Glucose Transporter Type 2 - metabolism</topic><topic>Glycoside Hydrolase Inhibitors</topic><topic>Humans</topic><topic>Lactase - antagonists & inhibitors</topic><topic>Lactase - metabolism</topic><topic>Medical sciences</topic><topic>Models, Animal</topic><topic>Monosaccharides - metabolism</topic><topic>Plant Extracts - pharmacology</topic><topic>Polyphenols - pharmacology</topic><topic>Postprandial Period - drug effects</topic><topic>Risk Factors</topic><topic>Sodium-Glucose Transporter 1 - genetics</topic><topic>Sodium-Glucose Transporter 1 - metabolism</topic><topic>Sucrase - antagonists & inhibitors</topic><topic>Sucrase - metabolism</topic><topic>Tea - chemistry</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Williamson, Gary</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular nutrition & food research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Williamson, Gary</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Possible effects of dietary polyphenols on sugar absorption and digestion</atitle><jtitle>Molecular nutrition & food research</jtitle><addtitle>Mol. Nutr. Food Res</addtitle><date>2013-01</date><risdate>2013</risdate><volume>57</volume><issue>1</issue><spage>48</spage><epage>57</epage><pages>48-57</pages><issn>1613-4125</issn><eissn>1613-4133</eissn><abstract>Excessive post‐prandial glucose excursions are a risk factor for developing diabetes, associated with impaired glucose tolerance. One way to limit the excursion is to inhibit the activity of digestive enzymes for glucose production and of the transporters responsible for glucose absorption. Flavonols, theaflavins, gallate esters, 5‐caffeoylqunic acid and proanthocyanidins inhibit α‐amylase activity. Anthocyanidins and catechin oxidation products, such as theaflavins and theasinsensins, inhibit maltase; sucrase is less strongly inhibited but anthocyanidins seem somewhat effective. Lactase is inhibited by green tea catechins. Once produced in the gut by digestion, glucose is absorbed by SGLT1 and GLUT2 transporters, inhibited by flavonols and flavonol glycosides, phlorizin and green tea catechins. These in vitro data are supported by oral glucose tolerance tests on animals, and by a limited number of human intervention studies on polyphenol‐rich foods. Acarbose is a drug whose mechanism of action is only through inhibition of α‐amylases and α‐glucosidases, and in intervention studies gives a 6% reduction in diabetes risk over 3 years. A lifetime intake of dietary polyphenols, assuming the same mechanism, has therefore a comparable potential to reduce diabetes risk, but more in vivo studies are required to fully test the effect of modulating post‐prandial blood glucose in humans.</abstract><cop>Weinheim</cop><pub>Blackwell Publishing Ltd</pub><pmid>23180627</pmid><doi>10.1002/mnfr.201200511</doi><tpages>10</tpages></addata></record> |
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subjects | Absorption Acarbose - pharmacology alpha-Amylases - antagonists & inhibitors alpha-Amylases - metabolism alpha-Glucosidases - metabolism Amylase Animals Anthocyanins - pharmacology Antioxidants - pharmacology Biflavonoids - pharmacology Biological and medical sciences Carbohydrate Metabolism - drug effects Catechin - pharmacology Diabetes Diabetes Mellitus - prevention & control Diabetes. Impaired glucose tolerance Diet Digestion - drug effects Disaccharidases - metabolism Disaccharide Endocrine pancreas. Apud cells (diseases) Endocrinopathies Feeding. Feeding behavior Flavonoid Flavonols - pharmacology Fundamental and applied biological sciences. Psychology Glucose - metabolism Glucose Tolerance Test Glucose transport Glucose Transporter Type 2 - genetics Glucose Transporter Type 2 - metabolism Glycoside Hydrolase Inhibitors Humans Lactase - antagonists & inhibitors Lactase - metabolism Medical sciences Models, Animal Monosaccharides - metabolism Plant Extracts - pharmacology Polyphenols - pharmacology Postprandial Period - drug effects Risk Factors Sodium-Glucose Transporter 1 - genetics Sodium-Glucose Transporter 1 - metabolism Sucrase - antagonists & inhibitors Sucrase - metabolism Tea - chemistry Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Possible effects of dietary polyphenols on sugar absorption and digestion |
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