Discriminative and aversive properties of beta-carboline-3-carboxylic acid ethyl ester, a benzodiazepine receptor inverse agonist, in rhesus monkeys.

Abstract:

:Rhesus monkeys were trained to discriminate injections of saline from those of beta-carboline-3-carboxylic acid ethyl ester (beta-CCE), a compound that binds to the benzodiazepine receptor, but often has actions opposite to those of the benzodiazepines. A benzodiazepine agonist midazolam and low doses of a specific benzodiazepine antagonist, Ro 15-1788, reversed the discriminative effects of beta-CCE. Higher doses of Ro 15-1788 produced stimulus effects similar to beta-CCE. In a separate experiment, monkeys responded to terminate intravenous infusions of beta-CCE, but not midazolam. This aversive effect of beta-CCE was reversed by Ro 15-1788. The behavioral effects of beta-CCE in these non-human primates are consistent with other data that have shown it to act on benzodiazepine receptors, and support the hypothesis that beta-CCE can be considered an inverse agonist at this receptor.

journal_name

Life Sci

journal_title

Life sciences

authors

Takada K,Winger G,Cook J,Larscheid P,Woods JH

doi

10.1016/0024-3205(86)90240-7

subject

Has Abstract

pub_date

1986-03-17 00:00:00

pages

1049-56

issue

11

eissn

0024-3205

issn

1879-0631

pii

0024-3205(86)90240-7

journal_volume

38

pub_type

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