Effects of the kappa opioid receptor antagonist MR-2266-BS on the acquisition of ethanol preference

Life Sci. 1990;46(16):1119-29. doi: 10.1016/0024-3205(90)90448-z.

Abstract

Using a paradigm by which rats forced to drink a weak ethanol solution (2.5% w/v) (conditioning session) develop ethanol preference in consecutive retention testing days, the effects of the administration of the kappa opioid antagonist MR-2266-BS, prior to or after the forced ethanol session, were studied. Pre-conditioning subcutaneous (s.c.) administration of 1 mg/kg of MR-2266-BS induced a decrease in subsequent ethanol consumption without significantly modifying the acquisition of ethanol preference. Post-conditioning administration of MR-2266-BS (0.1, 1, 5 or 10 mg/kg) induced both a dose-dependent reduction in ethanol consumption and in preference throughout the three following days. The results of the present study provide further support of the involvement of kappa-type opioids on drinking behavior, and suggest that kappa receptors may be involved in the consumption and development of preference to ethanol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Drinking / drug effects*
  • Animals
  • Benzomorphans / administration & dosage
  • Benzomorphans / pharmacology*
  • Conditioning, Psychological
  • Drinking Behavior / drug effects*
  • Male
  • Morphinans / pharmacology*
  • Narcotic Antagonists*
  • Rats
  • Rats, Inbred Strains
  • Receptors, Opioid, kappa
  • Regression Analysis
  • Sucrose / administration & dosage

Substances

  • Benzomorphans
  • Morphinans
  • Narcotic Antagonists
  • Receptors, Opioid, kappa
  • MR 2266
  • Sucrose