JPET

Home Help [Feedback] [For Subscribers] [Archive] [Search] --
 QUICK SEARCH:   [advanced]


     


Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on May 16, 2006; DOI: 10.1124/jpet.106.103168


This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
jpet.106.103168v1
318/2/907    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McMahon, L. R.
Right arrow Articles by France, C. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McMahon, L. R.
Right arrow Articles by France, C. P.


Received for publication February 21, 2006.
Revised May 12, 2006.
Accepted for publication May 15, 2006.

Efficacy and the discriminative stimulus effects of negative GABAA modulators, or inverse agonists, in diazepam-treated rhesus monkeys

Lance R. McMahon 1, Lisa R. Gerak 1, Charles P. France 2*

1 The University of Texas Health Science Center at San Antonio 2 University of Texas Health Science Center

* Address correspondence to: E-mail: france{at}uthscsa.edu

Abstract

In benzodiazepine (BZ)-dependent animals, the effects of negative GABAA modulators at BZ sites are not clearly related to differences in negative efficacy (i.e., inverse agonist activity). A flumazenil discriminative stimulus in diazepam (5.6 mg/kg/day)-treated rhesus monkeys was used to test the hypothesis that the effects of negative GABAA modulators at BZ sites do not vary as a function of efficacy in BZ-dependent animals. Negative GABAA modulators varying in efficacy were studied in combination with positive modulators acting at different modulatory sites (BZ, barbiturate, and neuroactive steroid sites). The negative modulators Ro 15-4513 and {beta}-CCE substituted for the flumazenil discriminative stimulus. Acute pretreatment with diazepam (3.2 and 10 mg/kg s.c.; in addition to 5.6 mg/kg/day p.o.), pentobarbital (3.2 and 10 mg/kg), or pregnanolone (1 and 3.2 mg/kg) attenuated the flumazenil discriminative stimulus and also attenuated the flumazenil-like discriminative stimulus effects of Ro 15-4513 and {beta}-CCE. Attenuation of the discriminative stimulus effects of flumazenil, Ro 15-4513 and {beta}-CCE did not systematically vary as a function of efficacy. When compared to their discriminative stimulus effects in untreated monkeys discriminating midazolam, both pregnanolone and pentobarbital were relatively more potent than diazepam in attenuating the discriminative stimulus effects of flumazenil, Ro 15-4513, and {beta}-CCE in diazepam-treated monkeys. These results show that the discriminative stimulus effects of BZ-site neutral and negative modulators are not different in BZ-dependent animals trained to discriminate flumazenil, and extend the results of a previous study showing that positive modulators acting at non-BZ sites are especially potent in attenuating the effects of flumazenil in diazepam-treated monkeys (i.e. diazepam withdrawal).


Key words: barbiturate, benzodiazepine, dependence, inverse agonist, neuroactive steroid, withdrawal





Home Help [Feedback] [For Subscribers] [Archive] [Search] --
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 2006 by the American Society for Pharmacology and Experimental Therapeutics.