Upregulation of SGLT-1 transport activity in rat jejunum induced by GLP-2 infusion in vivo

被引:209
|
作者
Cheeseman, CI [1 ]
机构
[1] Univ Alberta, Dept Physiol, Membrane Transport Grp, Edmonton, AB T6G 2H7, Canada
关键词
sodium-dependent glucose transporter; glucagon-like peptide-2; membrane transport; protein trafficking;
D O I
10.1152/ajpregu.1997.273.6.R1965
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The effect of in vivo infusion of the peptide hormone glucagon-like peptide 2 (GLP-2) on glucose transport across the rat jejunal brush-border membrane (BBM) was assessed using isolated membrane vesicles. A 2-h infusion of GLP-2 produced a marked acceleration of sodium-dependent glucose uptake into BBM vesicles with a significant overshoot. There was no change in vesicle space or permeability resulting from the hormone infusion. Kinetic analysis showed this stimulation to be the result of a threefold increase in the maximal rate of transport, with no consistent change in the affinity constant (K-m). The time course of this response showed that the effect was observable, but smaller, after only 30 min of hormone infusion and was maximal after 1 h. Sodium-dependent phloridzin binding to the membrane vesicles showed a parallel increase in maximal binding after 1 and 2 h of hormone infusion. Western blotting showed a similar increase in sodium-dependent glucose transporter 1 (SGLT-1) abundance. The effect of GLP-2 could be blocked by luminal brefeldin A or wortmannin. These results indicate that GLP-2 is able to induce trafficking of SGLT-1 from an intracellular pool into the BBM within 60 min and that phosphoinositol 3-kinase may well be involved in the intracellular signaling pathway in this response.
引用
收藏
页码:R1965 / R1971
页数:7
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