A critical review of the cannabinoid receptor as a drug target for obesity management
Article first published online: 20 AUG 2008
DOI: 10.1111/j.1467-789X.2008.00520.x
© 2008 The Authors. Journal compilation © 2008 International Association for the Study of Obesity
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How to Cite
Akbas, F., Gasteyger, C., Sjödin, A., Astrup, A. and Larsen, T. M. (2009), A critical review of the cannabinoid receptor as a drug target for obesity management. Obesity Reviews, 10: 58–67. doi: 10.1111/j.1467-789X.2008.00520.x
Publication History
- Issue published online: 23 DEC 2008
- Article first published online: 20 AUG 2008
- Received 29 April 2008; revised 14 July 2008; accepted 17 July 2008
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Keywords:
- Cannabinoid receptor antagonists;
- energy expenditure;
- obesity
Summary
The discovery of cannabinoids, with the well-known stimulatory effect of Cannabis sativa on appetite, has offered a new drug target for obesity treatment. Cannabinoids act on two different receptors: CB1 receptors which are sited in the brain and many peripheral tissues, and CB2 receptors which are primarily found in immune system cells. Cannabinoid receptor antagonists act centrally by blocking CB1 receptors, thereby reducing food intake. Moreover, they probably also act peripherally by increasing thermogenesis and therefore energy expenditure, as has been suggested by animal experiments. Despite these promising mechanisms of action, recent clinical studies examining the effect of the two CB1 receptor antagonists rimonabant and taranabant showed that the attained weight loss did not exceed that attained with other currently approved anti-obesity medications. Moreover, potentially severe psychiatric adverse effects limit their clinical use. As several new CB1 receptor antagonists are presently undergoing development, it remains to be elucidated to what extent they differ in terms of efficacy and safety. This review primarily discusses how close cannabinoid receptor antagonists are to the ideal anti-obesity drug, with respect to their mechanisms of action, clinical effectiveness and safety.

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