Green tea polyphenols inhibit the sodium-dependent glucose transporter of intestinal epithelial cells by a competitive mechanism

被引:298
作者
Kobayashi, Y
Suzuki, M
Satsu, H
Arai, S
Hara, Y
Suzuki, K
Miyamoto, Y
Shimizu, M
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Appl Biol Chem, Bunkyo Ku, Tokyo 1138657, Japan
[2] Mitsui Norin Co Ltd, Food Res Labs, Shizuoka 4260133, Japan
[3] Univ Shizuoka, Grad Sch Food & Nutr Sci, Shizuoka 4228526, Japan
关键词
green tea; polyphenol; glucose transporter; intestinal cell; diabetes;
D O I
10.1021/jf0006832
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Intestinal glucose uptake is mainly performed by the sodium-dependent glucose transporter, SGLT1. The transport activity of SGLT1 was markedly inhibited by green tea polyphenols, this inhibitory activity being most pronounced in polyphenols having galloyl residues such as epicatechin gallate (ECg) and epigallocatechin gallate (EGCg). Experiments using brush-border membrane vesicles obtained from the rabbit small intestine demonstrated that ECg inhibited SGLT1 in a competitive manner, although ECg itself was not transported via SGLT1. The present results suggest that tea polyphenols such as ECg interact with SGLT1 as antagonist-like molecules, possibly playing a role in controlling the dietary glucose uptake in the intestinal tract.
引用
收藏
页码:5618 / 5623
页数:6
相关论文
共 34 条
[2]   High blood glucose concentration is a risk factor for mortality in middle-aged nondiabetic men -: 20-year follow-up in the Whitehall Study, the Paris Prospective Study, and the Helsinki Policemen Study [J].
Balkau, B ;
Shipley, M ;
Jarrett, RJ ;
Pyörälä, K ;
Pyörälä, M ;
Forhan, A ;
Eschwège, E .
DIABETES CARE, 1998, 21 (03) :360-367
[3]   ACARBOSE - A PRELIMINARY REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES, AND THERAPEUTIC POTENTIAL [J].
CLISSOLD, SP ;
EDWARDS, C .
DRUGS, 1988, 35 (03) :214-243
[4]  
GANAPATHY V, 1981, J BIOL CHEM, V256, P118
[5]   THE INHIBITION OF ALPHA-AMYLASE BY TEA POLYPHENOLS [J].
HARA, Y ;
HONDA, M .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1990, 54 (08) :1939-1945
[6]   Is there a glycemic threshold for mortality risk? [J].
Harris, MI ;
Eastman, RC .
DIABETES CARE, 1998, 21 (03) :331-333
[7]   EXPRESSION CLONING AND CDNA SEQUENCING OF THE NA+/GLUCOSE COTRANSPORTER [J].
HEDIGER, MA ;
COADY, MJ ;
IKEDA, TS ;
WRIGHT, EM .
NATURE, 1987, 330 (6146) :379-381
[8]   INHIBITION OF RAT SMALL INTESTINAL SUCRASE AND ALPHA-GLUCOSIDASE ACTIVITIES BY TEA POLYPHENOLS [J].
HONDA, M ;
HARA, Y .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1993, 57 (01) :123-124
[9]   EVIDENCE THAT INCREASED GLUCOSE CYCLING IN ISLETS OF DIABETIC OB/OB MICE IS A PRIMARY FEATURE OF THE DISEASE [J].
KHAN, A ;
EFENDIC, S .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 269 (04) :E623-E626
[10]   Transmural potential changes associated with the in vitro absorption of theanine in the guinea pig intestine [J].
Kitaoka, S ;
Hayashi, H ;
Yokogoshi, H ;
Suzuki, Y .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1996, 60 (11) :1768-1771