Acute delta9-tetrahydrocannabinol exposure facilitates quinpirole-induced hyperlocomotion

Pharmacol Biochem Behav. 2005 May;81(1):71-7. doi: 10.1016/j.pbb.2005.02.004. Epub 2005 Apr 21.

Abstract

The endogenous cannabinoid system works as a feedback signal controlling dopamine-induced facilitation of motor behaviors. The present study explored whether a single acute stimulation of CB1 cannabinoid receptors with (-)-Delta9-tetrahydrocannabinol (THC, 5 mg kg(-1) i.p.) results in modifications in the sensitivity to the acute behavioral effects of the dopamine D2/D3 receptor agonist quinpirole (0.025, 0.25 and 1 mg kg(-1), s.c.) 24 h after THC administration. Cannabinoid pretreatment increased the sensitivity to quinpirole-induced hyperlocomotion 24 h after its administration. The data indicated that THC induced a desensitization of cannabinoid receptors, as revealed by a reduction in CB1 receptor-agonist induced GTP-gamma-S incorporation in striatal membranes. These results might be relevant for understanding the effect of cannabinoid exposure in dopamine-related neuropsychiatric disorders.

Publication types

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

MeSH terms

  • Animals
  • Dose-Response Relationship, Drug
  • Dronabinol / administration & dosage*
  • Drug Synergism
  • Male
  • Motor Activity / drug effects*
  • Motor Activity / physiology
  • Quinpirole / pharmacology*
  • Rats
  • Rats, Wistar
  • Receptor, Cannabinoid, CB1 / agonists
  • Receptor, Cannabinoid, CB1 / physiology

Substances

  • Receptor, Cannabinoid, CB1
  • Quinpirole
  • Dronabinol