The long-acting glucagon-like peptide-1 analogue, liraglutide, inhibits β-cell apoptosis in vitro

被引:141
作者
Bregenbolt, S
Moldrup, A
Blume, N
Karlsen, AE
Friedrichsen, BN
Tornhave, D
Knudsen, LB
Petersen, JS
机构
[1] Novo Nordisk AS, DK-2880 Bagsvaerd, Denmark
[2] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
关键词
liraglutide; GLP-1; beta-cells; apoptosis; cytokines; free fatty acids;
D O I
10.1016/j.bbrc.2005.03.013
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 here show that GLP-1 and the long-acting GLP-1 analogue, liraglutide, interfere with diabetes-associated apoptotic processes in the beta-cell. Studies using primary neonatal rat islets showed that native GLP-1 and liraglutide inhibited both cytokine- and free fatty acid-induced apoptosis in a dose-dependent manner. The anti-apoptotic effect of liraglutide was mediated by the GLP-1 receptor as the specific GLP-1 receptor antagonist, exendin(9-39), blocked the effects. The adenylate cyclase activator, forskolin, had an anti-apoptotic effect similar to those of GLP-1 and liraglutide indicating that the effect was cAMP-mediated. Blocking the PI3 kinase pathway using wortmannin but not the MAP kinase pathways by PD98059 inhibited the effects of liraglutide. In conclusion, GLP-1 receptor activation has anti-apoptotic effect on both cytokine, and free fatty acid-induced apoptosis in primary islet-cells, thus suggesting that the long-acting GLP-1 analogue, liraglutide, may be useful for retaining beta-cell mass in both type 1 and type 2 diabetic patients. (c) 2005 Published by Elsevier Inc.
引用
收藏
页码:577 / 584
页数:8
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