Role for Stearoyl-CoA Desaturase-1 in Leptin-Mediated Weight Loss

Author:

Cohen Paul1,Miyazaki Makoto2,Socci Nicholas D.13,Hagge-Greenberg Aaron1,Liedtke Wolfgang1,Soukas Alexander A.1,Sharma Ratnendra1,Hudgins Lisa C.4,Ntambi James M.25,Friedman Jeffrey M.16

Affiliation:

1. Laboratory of Molecular Genetics,

2. Department of Biochemistry and

3. Center for Studies in Physics and Biology,

4. Rogosin Institute,

5. Department of Nutritional Sciences, University of Wisconsin, Madison, WI 53706, USA.

6. Howard Hughes Medical Institute, The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.

Abstract

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 profiling 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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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