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Reinforcing Effects Of Compounds Lacking Intrinsic Efficacy At α1 Subunit-Containing GABAA Receptor Subtypes in Midazolam- But Not Cocaine-Experienced Rhesus Monkeys
Neuropsychopharmacology (2013)
  • Nina M Shinday
  • Eileen K. Sawyer
  • Dr. Bradford D. Fischer, PhD, Rowan University
  • Donna M. Platt
  • Stephanie C. Licata
  • John R. Atack
  • Gerard R. Dawson
  • David S. Reynolds
  • James K. Rowlett
Abstract
Benzodiazepines are prescribed widely but their utility is limited by unwanted side effects, including abuse potential. The mechanisms underlying the abuse-related effects of benzodiazepines are not well understood, although α1 subunit-containing GABAA receptors have been proposed to have a critical role. Here, we examine the reinforcing effects of several compounds that vary with respect to intrinsic efficacy at α2, α3, and α5 subunit-containing GABAA receptors but lack efficacy at α1 subunit-containing GABAA receptors (‘α1-sparing compounds'): MRK-623 (functional selectivity for α2/α3 subunit-containing receptors), TPA023B (functional selectivity for α2/α3/α5 subunit-containing receptors), and TP003 (functional selectivity for α3 subunit-containing receptors). The reinforcing effects of the α1-sparing compounds were compared with those of the non-selective benzodiazepine receptor partial agonist MRK-696, and non-selective benzodiazepine receptor full agonists, midazolam and lorazepam, in rhesus monkeys trained to self-administer midazolam or cocaine, under a progressive-ratio schedule of intravenous (i.v.) drug injection. The α1-sparing compounds were self-administered significantly above vehicle levels in monkeys maintained under a midazolam baseline, but not under a cocaine baseline over the dose ranges tested. Importantly, TP003 had significant reinforcing effects, albeit at lower levels of self-administration than non-selective benzodiazepine receptor agonists. Together, these results suggest that α1 subunit-containing GABAA receptors may have a role in the reinforcing effects of benzodiazepine-type compounds in monkeys with a history of stimulant self-administration, whereas α3 subunit-containing GABAA receptors may be important mediators of the reinforcing effects of benzodiazepine-type compounds in animals with a history of sedative-anxiolytic/benzodiazepine self-administration.
Keywords
  • benzodiazepine,
  • GABAA receptor,
  • alpha subunit,
  • self-administration,
  • drug history,
  • rhesus monkey (Macaca mulatta)
Publication Date
Spring May, 2013
DOI
10.1038/npp.2012.265
Citation Information
Nina M Shinday, Eileen K. Sawyer, Bradford D. Fischer, Donna M. Platt, et al.. "Reinforcing Effects Of Compounds Lacking Intrinsic Efficacy At α1 Subunit-Containing GABAA Receptor Subtypes in Midazolam- But Not Cocaine-Experienced Rhesus Monkeys" Neuropsychopharmacology Vol. 38 (2013) p. 1006 - 1014 ISSN: 0893-133X
Available at: http://works.bepress.com/bradford-fischer/2/