EVIDENCE THAT GLUCAGON STIMULATES INSULIN-SECRETION THROUGH ITS OWN RECEPTOR IN RATS

被引:68
|
作者
KAWAI, K
YOKOTA, C
OHASHI, S
WATANABE, Y
YAMASHITA, K
机构
[1] NATL INST BIOSCI & HUMAN TECHNOL,TSUKUBA,IBARAKI,JAPAN
[2] UNIV TSUKUBA,INST CLIN MED,DEPT INTERNAL MED,TSUKUBA,IBARAKI 305,JAPAN
关键词
GLUCAGON; INSULIN SECRETION; EXENDIN (9-39); GLP-1; PANCREAS PERFUSION;
D O I
10.1007/BF00400630
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Since glucagon-like peptide-1 (7-36) amide (7-37) (GLP-1) has been found to be a potent insulinotropic hormone, it has been postulated that glucagon stimulates insulin secretion from islet beta cells through the GLP-1 receptor. We therefore examined the effects of a GLP-1 receptor antagonist, exendin (9-39) amide, on glucagon- or GLP-1-stimulated insulin release from isolated perfused rat pancreas. When infusion of 100 nmol/l exendin (9-39) amide was started 5 min before that of 1 nmol/l glucagon, the stimulation of insulin release by glucagon was similar to that found in the control situation (preinfusion with vehicle alone), By contrast, when 0.3 nmol/l GLP-1 was used in the same experimental setting, exendin (9-39) amide clearly inhibited insulin release. These results indicate that glucagon stimulates insulin release mainly through glucagon receptors but not GLP-1 receptors on islet beta cells.
引用
收藏
页码:274 / 276
页数:3
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