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Role for stearoyl-CoA desaturase-1 in leptin-mediated weight loss.
Cohen, Paul; Miyazaki, Makoto; Socci, Nicholas D; Hagge-Greenberg, Aaron; Liedtke, Wolfgang; Soukas, Alexander A; Sharma, Ratnendra; Hudgins, Lisa C; Ntambi, James M; Friedman, Jeffrey M.
Affiliation
  • Cohen P; Laboratory of Molecular Genetics, Center for Studies in Physics and Biology, Rogosin Institute, Howard Hughes Medical Institute, The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.
Science ; 297(5579): 240-3, 2002 Jul 12.
Article de En | MEDLINE | ID: mdl-12114623
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.
Sujet(s)
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Acyl-(acyl-carrier-protein)desaturase / Perte de poids / Leptine / Foie Type d'étude: Prognostic_studies Limites: Animals Langue: En Journal: Science Année: 2002 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Acyl-(acyl-carrier-protein)desaturase / Perte de poids / Leptine / Foie Type d'étude: Prognostic_studies Limites: Animals Langue: En Journal: Science Année: 2002 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
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