Ethanol-induced conditioned place preference is expressed through a ventral tegmental area dependent mechanism

Behav Neurosci. 2005 Feb;119(1):213-23. doi: 10.1037/0735-7044.119.1.213.

Abstract

The authors examined the role of the ventral tegmental area (VTA) and nucleus accumbens (NAc) in the expression of ethanol-induced conditioned place preference (CPP). After cannulas were implanted, male DBA/2J mice underwent an unbiased Pavlovian-conditioning procedure for ethanol-induced CPP. Before preference testing, the mice were injected intra-VTA (Experiments 1 and 3) or intra-NAc (Experiment 2) with the nonselective opioid antagonist methylnaloxonium (0-ng, 375-ng, or 750-ng total infusion; Experiments 1 and 2) or the gamma aminobutyric acid (GABA(B)) agonist baclofen (0-ng, 25-ng, or 50-ng total infusion; Experiment 3). Intra-VTA methylnaloxonium or baclofen decreased ethanol-induced CPP, whereas intra-NAc methylnaloxonium had no effect. These findings indicate that the conditioned rewarding effect of ethanol is expressed through a VTA-dependent mechanism that involves both opioid and GABA(B) receptors.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Baclofen / administration & dosage
  • Baclofen / pharmacology
  • Central Nervous System Depressants / pharmacology*
  • Conditioning, Classical*
  • Ethanol / pharmacology*
  • GABA Agonists / administration & dosage
  • GABA Agonists / pharmacology
  • Male
  • Mice
  • Naloxone / administration & dosage
  • Naloxone / analogs & derivatives*
  • Naloxone / pharmacology
  • Quaternary Ammonium Compounds
  • Receptors, GABA-B / physiology
  • Receptors, Opioid / physiology
  • Reinforcement, Psychology
  • Space Perception
  • Ventral Tegmental Area / drug effects*
  • Ventral Tegmental Area / physiology*

Substances

  • Central Nervous System Depressants
  • GABA Agonists
  • Quaternary Ammonium Compounds
  • Receptors, GABA-B
  • Receptors, Opioid
  • Naloxone
  • Ethanol
  • N-methylnaloxone
  • Baclofen