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Rapamycin protects against high fat diet-induced obesity in C57BL/6J mice.

Abstract
Rapamycin (RAPA), an immunosuprpressive drug used extensively to prevent graft rejection in transplant patients, has been reported to inhibit adipogenesis in vitro. In this study, we investigated the anti-obesity effects of RAPA in C57BL/6J mice on a high-fat diet (HFD). Mice treated with RAPA (2 mg/kg per week for 16 weeks) had reduced body weight and epididymal fat pads/body weight, reduced daily food efficiency, and lower serum leptin and insulin levels compared with the HFD control mice. However, RAPA-treated mice were hyperphagic, demonstrating an increase in food intake. Dissection of RAPA-treated mice revealed a marked reduction in fatty liver scores, average fat cell size, and percentage of large adipocytes of retroperitoneal and epididymal white adipose tissue (RWAT and EWAT), compared to the HFD control mice. These results suggest that RAPA prevented the effect of the high-fat diet on the rate of accretion in body weight via reducing lipid accumulation, despite greater food intake. It is likely that RAPA may serve as a potential strategy for body weight control and/or anti-obesity therapy.
AuthorsGeng-Ruei Chang, Yi-Shin Chiu, Ying-Ying Wu, Wen-Ying Chen, Jiunn-Wang Liao, Te-Hsin Chao, Frank Chiahung Mao
JournalJournal of pharmacological sciences (J Pharmacol Sci) Vol. 109 Issue 4 Pg. 496-503 (Apr 2009) ISSN: 1347-8613 [Print] Japan
PMID19372632 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Blood Glucose
  • Dietary Fats
  • Immunosuppressive Agents
  • Insulin
  • Leptin
  • Sirolimus
Topics
  • Adipocytes (drug effects)
  • Animals
  • Blood Glucose (metabolism)
  • Body Weight (drug effects)
  • Cell Size (drug effects)
  • Diet
  • Dietary Fats (adverse effects)
  • Eating (drug effects)
  • Immunosuppressive Agents (pharmacology)
  • Insulin (blood)
  • Leptin (metabolism)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Obesity (pathology, prevention & control)
  • Organ Size (drug effects)
  • Sirolimus (pharmacology)

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