Metformin suppresses glucose-6-phosphatase expression by a complex I inhibition and AMPK activation-independent mechanism

被引:82
作者
Ota, Shinichi [1 ]
Horigome, Kazuhiko [1 ]
Ishii, Takayuki [1 ]
Nakai, Michio [1 ]
Hayashi, Koji [1 ]
Kawamura, Takao [1 ]
Kishino, Akiyoshi [1 ]
Taiji, Mutsuo [1 ]
Kimura, Toru [1 ]
机构
[1] Dainippon Sumitomo Pharma Co Ltd, Osaka 5540022, Japan
关键词
Metformin; Glucose-6-phosphatase; AMPK; Complex I; NDI1; Diabetes; PROTEIN-KINASE; RESPIRATORY-CHAIN; ADENOVIRUS; LIVER; GLUCONEOGENESIS; ADIPOCYTES; GENOME; CELLS;
D O I
10.1016/j.bbrc.2009.07.164
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
Metformin is widely used as a hypoglycemic agent for the treatment of type 2 diabetes. Both metformin and rotenone, an inhibitor of respiratory chain complex I, suppressed glucose-6-phosphatase (G6pc), a rate limiting enzyme of liver glucose production, mRNA expression in a rat hepatoma cell line accompanied by a reduction of intracellular ATP concentration and an activation of AMP-activated protein kinase (AMPK). When yeast NADH-quinone oxidoreductase 1 (NDI1) gene was introduced into the cells, neither inhibition of ATP synthesis nor activation of AMPK was induced by these agents. Interestingly, in contrast to rotenone treatment, G6pc mRNA down-regulation was observed in the NDI1 expressing cells after metformin treatment. Since NDI1 can functionally complement the complex I under the presence of metformin or rotenone, our results indicate that metformin induces down-regulation of G6pc expression through an inhibition of complex I and an activation of AMPK-independent mechanism. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:311 / 316
页数:6
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