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Research Article Free access | 10.1172/JCI3353

Resistance to adenovirally induced hyperleptinemia in rats. Comparison of ventromedial hypothalamic lesions and mutated leptin receptors.

K Koyama, M Shimabukuro, G Chen, M Y Wang, Y Lee, P S Kalra, M G Dube, S P Kalra, C B Newgard, and R H Unger

Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

Find articles by Koyama, K. in: JCI | PubMed | Google Scholar

Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

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Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

Find articles by Chen, G. in: JCI | PubMed | Google Scholar

Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

Find articles by Wang, M. in: JCI | PubMed | Google Scholar

Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

Find articles by Lee, Y. in: JCI | PubMed | Google Scholar

Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

Find articles by Kalra, P. in: JCI | PubMed | Google Scholar

Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

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Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

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Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

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Gifford Laboratories for Diabetes Research, Departments of Internal Medicine and Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.

Find articles by Unger, R. in: JCI | PubMed | Google Scholar

Published August 15, 1998 - More info

Published in Volume 102, Issue 4 on August 15, 1998
J Clin Invest. 1998;102(4):728–733. https://doi.org/10.1172/JCI3353.
© 1998 The American Society for Clinical Investigation
Published August 15, 1998 - Version history
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Abstract

Leptin regulates appetite and body weight via hypothalamic targets, but it can act directly on cultured pancreatic islets to regulate their fat metabolism. To obtain in vivo evidence that leptin may act peripherally as well as centrally, we compared the effect of adenovirally induced hyperleptinemia on food intake, body weight, and islet fat content in ventromedial hypothalamic-lesioned (VMHL) rats, sham-lesioned (SL) controls, and Zucker Diabetic Fatty (ZDF) rats in which the leptin receptor is mutated. Infusion with recombinant adenovirus containing the rat leptin cDNA increased plasma leptin by approximately 20 ng/ml in VMHL and ZDF rats but had no effect on their food intake, body weight, or fat tissue weight. Caloric matching of hyperphagic VMHL rats to SL controls did not reduce their resistance to hyperleptinemia. Whereas prediabetic ZDF rats had a fourfold elevation in islet fat, in VMHL rats islet fat was normal and none of them became diabetic. Isolated islets from ZDF rats were completely resistant to the lipopenic action of leptin, while VMHL islets exhibited 50% of the normal response; caloric matching of VMHL rats to SL controls increased leptin responsiveness of their islets to 92% of controls. We conclude that leptin regulation of adipocyte fat requires an intact VMH but that islet fat content is regulated independently of the VMH.

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