Rimonabant: a cannabinoid receptor blocker for the treatment of metabolic and cardiovascular risk factors

Nutr Metab Cardiovasc Dis. 2006 Mar;16(2):156-62. doi: 10.1016/j.numecd.2005.10.011. Epub 2006 Jan 18.

Abstract

Aims: The endocannabinoid system modulates synaptic neurotransmission centrally and peripherally and is involved in the brain pathways concerned with addiction, central regulation of body weight and adipose tissue function. The system is overactivated in animal models of obesity and nicotine use. This review discusses the role of rimonabant, a cannabinoid receptor 1 blocker, which has undergone Phase III clinical testing, in the treatment of obesity and tobacco dependence.

Data synthesis: Results of Phase III clinical trials have shown that rimonabant has promising efficacy in the treatment of obesity, dyslipidaemia and diabetes associated with obesity, in preventing weight gain following smoking cessation, and possibly in smoking cessation. No critical problems with the tolerance and safety of the compound have appeared in studies to date.

Conclusion: Rimonabant may prove to be a useful aid in the treatment of the most widespread cardiometabolic risk factors.

Publication types

  • Review

MeSH terms

  • Cannabinoid Receptor Antagonists*
  • Cardiovascular Diseases / etiology
  • Cardiovascular Diseases / prevention & control*
  • Clinical Trials, Phase III as Topic
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / drug therapy
  • Humans
  • Hyperlipidemias / complications
  • Hyperlipidemias / drug therapy
  • Metabolic Syndrome / complications
  • Metabolic Syndrome / drug therapy
  • Obesity / complications
  • Obesity / drug therapy*
  • Piperidines / pharmacology
  • Piperidines / therapeutic use*
  • Pyrazoles / pharmacology
  • Pyrazoles / therapeutic use*
  • Rimonabant
  • Risk Factors
  • Smoking Cessation
  • Tobacco Use Disorder / drug therapy*
  • Treatment Outcome
  • Weight Gain / drug effects*
  • Weight Gain / physiology

Substances

  • Cannabinoid Receptor Antagonists
  • Piperidines
  • Pyrazoles
  • Rimonabant