Ethanol and the GABA receptor complex: Studies with the partial inverse benzodiazepine receptor agonist Ro 15-4513

John R. Glowa, Jacqueline Crawley, Peter D. Suzdak, Steven M. Paul

Research output: Contribution to journalArticle

45 Scopus citations

Abstract

Ethanol potentiates GABA-receptor-medated Cl- ion flux in vitro and, at similar concentrations, has anxiolytic and intoxicating properties in vivo. The imidazobenzodiazepine, Ro 15-4513 (ethyl-8-azido-5-6-dihydro-5-meth-6-oxo-4H-imidazo (1,5-a)(1,4)benzodiazepine-3-carboxylate), is a potent partial inverse agonist of the benzodiazepine/GABA receptor which can antagonize the in vitro actions of ethanol in potentiating GABA receptor-mediated Cl- ion flux. Moreover, several of the behavioral effects of ethanol are also antagonized by Ro 15-4513, and these effects can be demonstrated in several paradigms at doses of Ro 15-4513 that do not produce opposite behavioral effects. In contrast, in our studies, other benzodiazepine receptor antagonist and inverse agonists, including Ro 15-1787, FG-7142, and β-CCE were not able to antagonize these biochemical or behavioral effects by ethanol at doses that were without intrinsic effects. However, both Ro 15-1788 and β-CCE blocked the antagonism of ethanol's effects by Ro 15-4513, suggesting a role for the GABA receptor complex in the actions of ethanol. These studies provide further evidence that GABAergic neurones may mediate at least some of the behavioral and biochemical actions of low-to-moderate doses of ethanol.

Original languageEnglish (US)
Pages (from-to)767-772
Number of pages6
JournalPharmacology, Biochemistry and Behavior
Volume31
Issue number3
DOIs
StatePublished - 1988
Externally publishedYes

Keywords

  • Conflict
  • Ethanol
  • GABA
  • Intoxication
  • Mice
  • Rats
  • Ro 15-4513
  • Schedule-controlled responding

ASJC Scopus subject areas

  • Biochemistry
  • Behavioral Neuroscience
  • Pharmacology

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