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Adiponectin suppresses hepatic SREBP1c expression in an AdipoR1/LKB1/AMPK dependent pathway
Authors:Motoharu Awazawa  Kohjiro Ueki  Kazunori Inabe  Kazuma Kaneko  Nabeel Bardeesy  Ryozo Nagai
Affiliation:a Department of Metabolic Diseases, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan
b National Institute of Health and Nutrition, 1-23-1 Toyama, Sinjuku-ku, Tokyo 162-8636, Japan
c Drug Discovery Research, Astellas Pharma Inc., 21 Miyukigaoka, Tsukuba, Ibaraki 305-8585, Japan
d Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA
e Department of Gastroenterology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan
f Department of Cardiovascular Diseases, Graduate School of Medicine, University of Tokyo, Tokyo, Japan
Abstract:Adiponectin, one of the insulin-sensitizing adipokines, has been shown to activate fatty acid oxidation in liver and skeletal muscle, thus maintaining insulin sensitivity. However, the precise roles of adiponectin in fatty acid synthesis are poorly understood. Here we show that adiponectin administration acutely suppresses expression of sterol regulatory element-binding protein (SREBP) 1c, the master regulator which controls and upregulates the enzymes involved in fatty acid synthesis, in the liver of +Leprdb/+Leprdb (db/db) mouse as well as in cultured hepatocytes. We also show that adiponectin suppresses SREBP1c by AdipoR1, one of the functional receptors for adiponetin, and furthermore that suppressing either AMP-activated protein kinase (AMPK) via its upstream kinase LKB1 deletion cancels the negative effect of adiponectin on SREBP1c expression. These data show that adiponectin suppresses SREBP1c through the AdipoR1/LKB1/AMPK pathway, and suggest a possible role for adiponectin in the regulation of hepatic fatty acid synthesis.
Keywords:Diabetes mellitus   Adipocytokine   Adiponectin   SREBP1c   Fatty acid synthesis   AMPK
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