Endotoxin and cytokines induce expression of leptin, the ob gene product, in hamsters. (original) (raw)

Research Article Free access | 10.1172/JCI118653

C Zhao, J Fuller, A Pollack, A Moser, J Friedman, and K R Feingold

Department of Medicine, University of California, San Francisco, USA. grunfld@itsa.ucsf.edu

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Department of Medicine, University of California, San Francisco, USA. grunfld@itsa.ucsf.edu

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Department of Medicine, University of California, San Francisco, USA. grunfld@itsa.ucsf.edu

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Department of Medicine, University of California, San Francisco, USA. grunfld@itsa.ucsf.edu

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Department of Medicine, University of California, San Francisco, USA. grunfld@itsa.ucsf.edu

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Department of Medicine, University of California, San Francisco, USA. grunfld@itsa.ucsf.edu

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Department of Medicine, University of California, San Francisco, USA. grunfld@itsa.ucsf.edu

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Published May 1, 1996 -More info

Published May 1, 1996 -Version history

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Abstract

The expression of leptin, the ob gene product, is increased in adipose tissue in response to feeding and energy repletion, while leptin decreases food intake. Because adipose tissue gene expression is regulated by cytokines induced during infection and because infection is associated with anorexia, we tested whether induction of leptin might occur during the host response to infection. Administration of endotoxin (LPS), a model for gram negative infections, induces profound anorexia and weight loss in hamsters. In fasted adipose tissue to levels similar to fed control animals. There is a strong inverse correlation between mRNA levels of leptin and subsequent food intake. TNF and IL-1, mediators of the host response to LPS, also induced anorexia and increased levels of leptin in mRNA in adipose tissue. As assessed by immuknoprecipitation and Western blotting, circulating leptin protein is regulated by LPS and cytokines in parallel to regulation of adipose tissue leptin mRNA. Induction of leptin during the host response to infection may contribute to the anorexia of infection.

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