Chronic cannabinoid administration to periadolescent rats modulates the metabolic response to acute cocaine in the adult brain

Mol Imaging Biol. 2011 Jun;13(3):411-415. doi: 10.1007/s11307-010-0388-8.

Abstract

Purpose: To analyze brain metabolic response to acute cocaine in male and female Wistar rats with or without a history of cannabinoid exposure during periadolescence.

Procedures: The synthetic cannabinoid agonist CP 55,940 (CP) or its vehicle (VH), were administered to male and female rats during periadolescence. When these animals reached adulthood, saline and cocaine-induced changes in 2-deoxy-2-[¹⁸F]fluoro-D-: glucose (FDG) uptake were studied by positron emission tomography.

Results: The baseline (post-saline) metabolism in the septal nuclei was higher in CP-females than in VH-females, although septal metabolism was lower in CP-females after cocaine, reaching similar values to those of VH-females at baseline. Cocaine did not affect metabolism in VH-females. Periadolescent cannabinoid treatment did not influence baseline metabolism in males although cocaine reduced the FDG uptake in the dorsal striatum of males that received the VH but not CP.

Conclusions: These results suggest that cannabinoids during periadolescence modify baseline and cocaine-evoked brain metabolism in a sex-dependent manner. In the case of CP-females, the involvement of septal metabolic alterations in their susceptibility to the rewarding effects of cocaine should be further investigated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / drug effects
  • Aging / metabolism*
  • Animals
  • Brain / drug effects*
  • Brain / metabolism*
  • Cannabinoids / administration & dosage*
  • Cannabinoids / pharmacology*
  • Cocaine / administration & dosage*
  • Cocaine / pharmacology*
  • Female
  • Magnetic Resonance Imaging
  • Male
  • Neostriatum / drug effects
  • Neostriatum / metabolism
  • Rats
  • Rats, Wistar
  • Septal Nuclei / drug effects
  • Septal Nuclei / metabolism

Substances

  • Cannabinoids
  • Cocaine