Nutritional regulation of glucagon-like peptide-1 secretion

被引:177
|
作者
Tolhurst, Gwen
Reimann, Frank
Gribble, Fiona M. [1 ]
机构
[1] Addenbrookes Hosp, Cambridge Inst Med Res, Cambridge CB2 0XY, England
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2009年 / 587卷 / 01期
基金
英国惠康基金;
关键词
DEPENDENT INSULINOTROPIC PEPTIDE; PANCREATIC BETA-CELL; ENTEROENDOCRINE CELLS; GLYCEMIC CONTROL; GLP-1; RAT; RECEPTOR; RELEASE; GUT; TRANSCRIPTION;
D O I
10.1113/jphysiol.2008.164012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glucagon-like peptide-1 (GLP-1), released from L-cells in the intestinal epithelium, plays an important role in postprandial glucose homeostasis and appetite control. Following the recent therapeutic successes of antidiabetic drugs aimed at either mimicking GLP-1 or preventing its degradation, attention is now turning towards the L-cell, and addressing whether it would be both possible and beneficial to stimulate the endogenous release of GLP-1 in vivo. Understanding the mechanisms underlying GLP-1 release from L-cells is key to this type of approach, and the use of cell line models has led to the identification of a variety of pathways that may underlie the physiological responses of L-cells to food ingestion. This review focuses on our current understanding of the signalling mechanisms that underlie L-cell nutrient responsiveness.
引用
收藏
页码:27 / 32
页数:6
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