Interaction of quercetin glucosides with the intestinal sodium/glucose co-transporter (SGLT-1)

被引:88
作者
Ader, P [1 ]
Blöck, M [1 ]
Pietzsch, S [1 ]
Wolffram, S [1 ]
机构
[1] Univ Kiel, Inst Anim Nutr Physiol & Metab, D-24098 Kiel, Germany
关键词
flavonoids; quercetin; glucoside; absorption; small intestine; sodium/glucose co-transporter-1;
D O I
10.1016/S0304-3835(00)00645-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently it has been postulated that flavonoid glucosides may be absorbed by the small intestine via the SGLT-1. Therefore, we applied an in vitro mucosal uptake method to investigate mucosal uptake of the non-metabolisable glucose analogue methyl-alpha -D-glucopyranoside (MDG) as influenced by quercetin-3-glucoside (isoquercitrin) and quercetin-4'-glucoside (spiraeosid). We found that both glucosides significantly inhibited SGLT-1 mediated MDG uptake whereas the aglycon quercetin or the quercetin-3-rhamnoglucoside (rutin) were ineffective. Calculated apparent kinetic parameters (K-m, V-max) of initial Na+-dependent MDG uptake by the jejunal mucosa indicate a competitive type of inhibition. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:175 / 180
页数:6
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