Article abstract
Nature Medicine 14, 667 - 675 (2008)
Published online: 1 June 2008 | doi:10.1038/nm1775
Leptin controls adipose tissue lipogenesis via central, STAT3–independent mechanisms
Christoph Buettner1, Evan D Muse2,3,4, Andrew Cheng2,3, Linghong Chen1, Thomas Scherer1, Alessandro Pocai3,4,6, Kai Su1, Bob Cheng1, Xiasong Li3,4, Judith Harvey-White5, Gary J Schwartz3,4, George Kunos5 & Luciano Rossetti2,3,4,6
Abstract
Leptin (encoded by Lep) controls body weight by regulating food intake and fuel partitioning. Obesity is characterized by leptin resistance and increased endocannabinoid tone. Here we show that leptin infused into the mediobasal hypothalamus (MBH) of rats inhibits white adipose tissue (WAT) lipogenesis, which occurs independently of signal transducer and activator of transcription-3 (STAT3) signaling. Correspondingly, transgenic inactivation of STAT3 signaling by mutation of the leptin receptor (s/s mice) leads to reduced adipose mass compared to db/db mice (complete abrogation of leptin receptor signaling). Conversely, the ability of hypothalamic leptin to suppress WAT lipogenesis in rats is lost when hypothalamic phosphoinositide 3-kinase signaling is prevented or when sympathetic denervation of adipose tissue is performed. MBH leptin suppresses the endocannabinoid anandamide in WAT, and, when this suppression of endocannabinoid tone is prevented by systemic CB1 receptor activation, MBH leptin fails to suppress WAT lipogenesis. These data suggest that the increased endocannabinoid tone observed in obesity is linked to a failure of central leptin signaling to restrain peripheral endocannabinoids.
- Department of Medicine, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1005, New York, New York 10029, USA.
- Department of Molecular Pharmacology, Albert Einstein College of Medicine, 1300 Morris Park, Bronx, New York 10461, USA.
- Department of Medicine, Albert Einstein College of Medicine, 1300 Morris Park, Bronx, New York 10461, USA.
- Diabetes Research and Training Center, Albert Einstein College of Medicine, 1300 Morris Park, Bronx, New York 10461, USA.
- US National Institute on Alcohol Abuse & Alcoholism, US National Institutes of Health, 5625 Fishers Lane, Bethesda, Maryland 20892, USA.
- Current address: Merck, 126 East Lincoln Avenue, Rahway, New Jersey 07065, USA.
Correspondence to: Christoph Buettner1 e-mail: christoph.buettner@mssm.edu
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