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Reinforcing and discriminative stimulus effects of the neuroactive steroids pregnanolone and Co 8-7071 in rhesus monkeys

dc.contributor.authorCarter, Richard B.en_US
dc.contributor.authorWood, Paul L.en_US
dc.contributor.authorRowlett, James K.en_US
dc.contributor.authorWinger, Gail D.en_US
dc.contributor.authorWoods, James H.en_US
dc.contributor.authorWoolverton, William L.en_US
dc.date.accessioned2006-09-08T19:49:41Z
dc.date.available2006-09-08T19:49:41Z
dc.date.issued1999-07en_US
dc.identifier.citationRowlett, James K.; Winger, Gail; Carter, Richard B.; Wood, Paul L.; Woods, James H.; Woolverton, W. L.; (1999). "Reinforcing and discriminative stimulus effects of the neuroactive steroids pregnanolone and Co 8-7071 in rhesus monkeys." Psychopharmacology 145(2): 205-212. <http://hdl.handle.net/2027.42/41966>en_US
dc.identifier.issn0033-3158en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/41966
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=10463322&dopt=citationen_US
dc.description.abstract  Rationale and Objectives : The present study was designed to assess possible abuse-related effects of the endogenous neuroactive steroid pregnanolone (3α-hydroxy-5β-pregnan-20-one) and the orally bioavailable, water-soluble neuroactive steroid pro-drug Co 8-7071 (3α,21-dihydroxy-3β-trifluoromethyl-5β-pregnan-20-one, 21-hemisuccinate). Methods : Four rhesus monkeys were prepared with chronic intravenous (IV) catheters and trained to press a lever under a ten-response fixed-ratio (FR) schedule of methohexital injection (0.1 mg/kg per injection). Three rhesus monkeys were trained to discriminate intragastric infusions of pentobarbital (10 mg/kg) from saline infusions under a FR5 schedule of stimulus-shock termination. Results : At least two doses of pregnanolone (0.003–0.1 mg/kg per injection) maintained injections per session above saline levels in the four monkeys tested, whereas Co 8-7071 (0.01–1.0 mg/kg per injection) maintained injections per session above saline levels in two of four monkeys at relatively low levels of injections per session. In rhesus monkeys trained to discriminate pentobarbital, IV pregnanolone injections (0.1–1.7 mg/kg, 5-min presession) dose-dependently reproduced the discriminative stimulus effects of pentobarbital in all monkeys tested. Intravenous administration of Co 8-7071 (1–10 mg/kg, 5-min presession) resulted in a dose-dependent increase to >80% pentobarbital-appropriate responding in two of three monkeys tested. Following intragastric infusions of Co 8-7071 (1.0–30 mg/kg), ≥80% pentobarbital-appropriate responding occurred in one out of three monkeys at 10 mg/kg when administered 60 min before the session. When administered 120 min before the session, however, 10–30 mg/kg Co 8-7071 reproduced the discriminative stimulus effects of pentobarbital in each of the three monkeys tested. Conclusions : These data demonstrate barbiturate-like abuse-related effects that differed between two pregnane steroids. Whereas pregnanolone functioned as a reinforcer, suggesting that this compound has abuse potential, Co 8-7071 did not, despite having pentobarbital-like discriminative effects.en_US
dc.format.extent88492 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Springer-Verlag Berlin Heidelbergen_US
dc.subject.otherRhesus Monkeyen_US
dc.subject.otherDiscriminative Stimulus Effectsen_US
dc.subject.otherKey Words Neuroactive Steroiden_US
dc.subject.otherBarbiturateen_US
dc.subject.otherLegacyen_US
dc.subject.otherSelf-administrationen_US
dc.titleReinforcing and discriminative stimulus effects of the neuroactive steroids pregnanolone and Co 8-7071 in rhesus monkeysen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPsychiatryen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Pharmacology and Psychology, University of Michigan, Ann Arbor, Michigan, USA, US,en_US
dc.contributor.affiliationumDepartments of Pharmacology and Psychology, University of Michigan, Ann Arbor, Michigan, USA, US,en_US
dc.contributor.affiliationotherDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, 2500 North State Street, Jackson, MI 39216, USA Fax: +1-601-984-5899, US,en_US
dc.contributor.affiliationotherCoCensys, Inc., Irvine, California, USA, US,en_US
dc.contributor.affiliationotherCoCensys, Inc., Irvine, California, USA, US,en_US
dc.contributor.affiliationotherDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, 2500 North State Street, Jackson, MI 39216, USA Fax: +1-601-984-5899, US,en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid10463322en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/41966/1/213-145-2-205_91450205.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s002130051050en_US
dc.identifier.sourcePsychopharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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