The acyclic CB1R inverse agonist taranabant mediates weight loss by increasing energy expenditure and decreasing caloric intake

Cell Metab. 2008 Jan;7(1):68-78. doi: 10.1016/j.cmet.2007.11.012.

Abstract

Cannabinoid 1 receptor (CB1R) inverse agonists are emerging as a potential obesity therapy. However, the physiological mechanisms by which these agents modulate human energy balance are incompletely elucidated. Here, we describe a comprehensive clinical research study of taranabant, a structurally novel acyclic CB1R inverse agonist. Positron emission tomography imaging using the selective CB1R tracer [(18)F]MK-9470 confirmed central nervous system receptor occupancy levels ( approximately 10%-40%) associated with energy balance/weight-loss effects in animals. In a 12-week weight-loss study, taranabant induced statistically significant weight loss compared to placebo in obese subjects over the entire range of evaluated doses (0.5, 2, 4, and 6 mg once per day) (p < 0.001). Taranabant treatment was associated with dose-related increased incidence of clinical adverse events, including mild to moderate gastrointestinal and psychiatric effects. Mechanism-of-action studies suggest that engagement of the CB1R by taranabant leads to weight loss by reducing food intake and increasing energy expenditure and fat oxidation.

Trial registration: ClinicalTrials.gov NCT00109148.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Amides / pharmacology*
  • Amides / therapeutic use
  • Brain / drug effects
  • Brain / metabolism
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Energy Intake / drug effects*
  • Energy Metabolism / drug effects*
  • Fats / metabolism
  • Humans
  • Middle Aged
  • Positron-Emission Tomography
  • Pyridines / pharmacology*
  • Pyridines / therapeutic use
  • Receptor, Cannabinoid, CB1 / agonists*
  • Weight Loss / drug effects*

Substances

  • Amides
  • Fats
  • Pyridines
  • Receptor, Cannabinoid, CB1
  • N-(3-(4-chlorophenyl)-2-(3-cyanophenyl)-1-methylpropyl)-2-methyl-2-((5-(trifluoromethyl)pyridin-2-yl)oxy)propanamide

Associated data

  • ClinicalTrials.gov/NCT00109148