The cannabinoid 1-receptor silent antagonist O-2050 attenuates preference for high-fat diet and activated astrocytes in mice

J Pharmacol Sci. 2010;112(3):369-72. doi: 10.1254/jphs.09326sc. Epub 2010 Feb 18.

Abstract

Endocannabinoids have been shown to activate reward-related feeding and to promote astrocytic differentiation. We investigated whether high-fat diet (HFD) intake produced a preference for HFD via an endocannabinoid-dependent mechanism. In the conditioned place preference test, the 2-week HFD-intake group showed preference for HFD and had increased expression of a marker for reactive astrocytes, glial fibrillary acid protein (GFAP), in the hypothalamus. The cannabinoid CB(1)-receptor antagonist O-2050 reduced the preference for HFD and expression of GFAP in the hypothalamus. These results suggested that HFD intake led to the development of a preference for HFD via astrocytic CB(1) receptors in the hypothalamus.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / drug effects*
  • Astrocytes / metabolism
  • Dietary Fats / administration & dosage*
  • Dronabinol / analogs & derivatives*
  • Dronabinol / pharmacology
  • Feeding Behavior / drug effects
  • Feeding Behavior / physiology
  • Feeding Behavior / psychology
  • Food Preferences / drug effects*
  • Food Preferences / physiology
  • Food Preferences / psychology
  • Hypothalamus / cytology
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism
  • Male
  • Mice
  • Mice, Inbred ICR
  • Pyrans / pharmacology*
  • Receptor, Cannabinoid, CB1 / antagonists & inhibitors*
  • Receptor, Cannabinoid, CB1 / physiology

Substances

  • (6aR,10aR)-3-(1-methansulfonylamino-4-hexyn-6-yl)6a,7,10,10a-tetrahydro-6,6,9-trimethyl-6H-dibenzo(b,d)pyran
  • Dietary Fats
  • Pyrans
  • Receptor, Cannabinoid, CB1
  • Dronabinol