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 Scijournal_title
Life sciencesauthors
Takada K,Winger G,Cook J,Larscheid P,Woods JHdoi
10.1016/0024-3205(86)90240-7subject
Has Abstractpub_date
1986-03-17 00:00:00pages
1049-56issue
11eissn
0024-3205issn
1879-0631pii
0024-3205(86)90240-7journal_volume
38pub_type
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