Role for stearoyl-CoA desaturase-1 in leptin-mediated weight loss

被引:622
作者
Cohen, P
Miyazaki, M
Socci, ND
Hagge-Greenberg, A
Liedtke, W
Soukas, AA
Sharma, R
Hudgins, LC
Ntambi, JM
Friedman, JM
机构
[1] Rockefeller Univ, Mol Genet Lab, New York, NY 10021 USA
[2] Rockefeller Univ, Ctr Studies Phys & Biol, New York, NY 10021 USA
[3] Rockefeller Univ, Rogosin Inst, New York, NY 10021 USA
[4] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10021 USA
[5] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[6] Univ Wisconsin, Dept Nutr Sci, Madison, WI 53706 USA
关键词
D O I
10.1126/science.1071527
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Leptin elicits a metabolic response that cannot be explained by its anorectic effects alone. To examine the mechanism underlying leptin's metabolic actions, we used transcription pro ling to identify leptin-regulated genes in ob/ob liver. Leptin was found to specifically repress RNA levels and enzymatic activity of hepatic stearoyl-CoA desaturase-1 (SCD-1), which catalyzes the biosynthesis of monounsaturated fatty acids. Mice lacking SCD-1 were lean and hypermetabolic. ob/ob mice with mutations in SCD-1 were significantly less obese than ob/ob controls and had markedly increased energy expenditure. ob/ob mice with mutations in SCD-1 had histologically normal livers with significantly reduced triglyceride storage and VLDL ( very low density lipoprotein) production. These findings suggest that down-regulation of SCD-1 is an important component of leptin's metabolic actions.
引用
收藏
页码:240 / 243
页数:5
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