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Review
. 2020 Jun 4;10(6):855.
doi: 10.3390/biom10060855.

Targeting the Endocannabinoid CB1 Receptor to Treat Body Weight Disorders: A Preclinical and Clinical Review of the Therapeutic Potential of Past and Present CB1 Drugs

Affiliations
Review

Targeting the Endocannabinoid CB1 Receptor to Treat Body Weight Disorders: A Preclinical and Clinical Review of the Therapeutic Potential of Past and Present CB1 Drugs

Thomas Murphy et al. Biomolecules. .

Abstract

Obesity rates are increasing worldwide and there is a need for novel therapeutic treatment options. The endocannabinoid system has been linked to homeostatic processes, including metabolism, food intake, and the regulation of body weight. Rimonabant, an inverse agonist for the cannabinoid CB1 receptor, was effective at producing weight loss in obese subjects. However, due to adverse psychiatric side effects, rimonabant was removed from the market. More recently, we reported an inverse relationship between cannabis use and BMI, which has now been duplicated by several groups. As those results may appear contradictory, we review here preclinical and clinical studies that have studied the impact on body weight of various cannabinoid CB1 drugs. Notably, we will review the impact of CB1 inverse agonists, agonists, partial agonists, and neutral antagonists. Those findings clearly point out the cannabinoid CB1 as a potential effective target for the treatment of obesity. Recent preclinical studies suggest that ligands targeting the CB1 may retain the therapeutic potential of rimonabant without the negative side effect profile. Such approaches should be tested in clinical trials for validation.

Keywords: BMI; cannabinoid; cannabis; clinical; obesity; preclinical; weight loss.

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Conflict of interest statement

The authors declare no conflict of interest. Bernard Le Foll has received some in-kind donation of cannabis product from Aurora. Bernard Le Foll has performed research with industry funding obtained from Canopy (through research grants handled by CAMH or University of Toronto). Bernard Le Foll has received in-kind donations of nabiximols from GW Pharma for past studies funded by CIHR and NIH. The other grants obtained by Bernard Le Foll are unrelated to the present work.

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