A role for the gut-to-brain GLP-1-dependent axis in the control of metabolism

被引:37
作者
Burcelin, Remy [1 ]
Serino, Matteo [1 ]
Cabou, Cendrine [1 ]
机构
[1] INSERM, IFR31, U858, Rangueil Inst Mol Med,I2MR, F-84225 Toulouse, France
关键词
GLUCAGON-LIKE PEPTIDE-1; NITRIC-OXIDE SYNTHASE; DEPENDENT INSULINOTROPIC POLYPEPTIDE; GASTRIC-ACID-SECRETION; PANCREATIC BETA-CELLS; ARTERIAL-BLOOD FLOW; PERFUSED RAT ILEUM; GLUCOSE-UTILIZATION; NERVOUS-SYSTEM; 7-36; AMIDE;
D O I
10.1016/j.coph.2009.09.003
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Over the past years tremendous amounts of clinical and fundamental data have been generated about GLP-1 and related therapeutic strategies for the treatment of type 2 diabetes. However, the cellular and physiological mechanisms through which GLP-1 is secreted, controls glycemia, and behaves as a therapeutic agent are certainly unclear. This is due to the dogma that proposes that upon glucose absorption GLP-1 is secreted into the hepatoportal blood flow, binds to its receptor at the surface of the insulin secreting 0 cells, and triggers the secretion of insulin to control glycemia. However, these events have never been demonstrated sequentially for the control of glycemia. This conclusion is supported by a growing number of evidences that point out that the enteric and the central nervous systems are main actors in the control of GLP-1 action. This involves the triggering of the gut-to-brain and to periphery axis where nutrients regulate the release of GLP-1 and activate the tightly regulated enteric and cerebral neuronal circuits. These integrate and redistribute the GLP-1 dependent signals toward numerous targeted tissues. We will review some of them.
引用
收藏
页码:744 / 752
页数:9
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