Glucagon-like peptide-1(7-36) amide enhances insulin-stimulated glucose uptake and decreases intracellular cAMP content in isolated rat adipocytes

被引:37
|
作者
Miki, H
Namba, M
Nishimura, T
Mineo, I
Matsumura, T
Miyagawa, J
Nakajima, H
Kuwajima, M
Hanafusa, T
Matsuzawa, Y
机构
[1] OTEMAE HOSP,OSAKA 540,JAPAN
[2] UNIV TOKUSHIMA,SCH MED,DEPT LAB MED,TOKUSHIMA 770,JAPAN
来源
关键词
glucagon-like peptide-1(7-36)amide; glucose uptake; cAMP; adipocyte; (rat);
D O I
10.1016/0167-4889(96)00032-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We investigated the effect of GLPs on glucose uptake in isolated rat adipocytes, GLP-1(7-36)amide significantly enhanced glucose uptake in the presence of 1 nM insulin. GLP-1(7-36)amide at 15 nM increased glucose uptake maximally by 56.4% as compared with 1 nM insulin alone (P < 0.01), In contrast, with less than 1 nM insulin or without insulin GLP-1(7-36)amide showed no effect on glucose uptake. Full-sequence GLP-1(1-37) at 15 nM in the presence of 1 nM insulin increased glucose uptake by 24.6% as compared with 1 nM insulin alone (P < 0.05). GLP-2 showed no effect on glucose uptake. Further, we examined the effect of GLP-1(7-36)amide on cAMP content in isolated rat adipocytes, Insulin at 1 nM caused a significant decrease of cAMP content, The combination of 15 nM GLP-1(7-36)amide and 1 nM insulin caused a further reduction of cAMP content. These data indicate that GLP-1(7-36)amide possesses augmentative effects on insulin action in isolated rat adipocytes. Furthermore, it is suggested that the stimulatory effect of GLP-1(7-36)amide occurs through the reduction of intracellular cAMP content.
引用
收藏
页码:132 / 136
页数:5
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