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Selective blockade of the discriminative stimulus effects of pentobarbital in pigeons

dc.contributor.authorHerling, Seymoreen_US
dc.contributor.authorWinger, Gail D.en_US
dc.date.accessioned2006-09-11T17:46:06Z
dc.date.available2006-09-11T17:46:06Z
dc.date.issued1981-11en_US
dc.identifier.citationHerling, Seymore; Winger, Gail; (1981). "Selective blockade of the discriminative stimulus effects of pentobarbital in pigeons." Psychopharmacology 75(3): 321-323. <http://hdl.handle.net/2027.42/46426>en_US
dc.identifier.issn1432-2072en_US
dc.identifier.issn0033-3158en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46426
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6798625&dopt=citationen_US
dc.description.abstractThe ability of CNS stimulants to block the discriminative effects of pentobarbital was studied in pigeons trained to discriminate IM pentobarbital (5 mg/kg) from saline. Pentobarbital, when administered alone, consistently produced greater than 90% pentobarbital-appropriate responding. The concomitant administration of pentobarbital and increasing doses of bemegride or pentylenetetrazol resulted in a dose-related decrease in pentobarbital-appropriate responses. In contrast, picrotoxin, another CNS stimulant, had little or no effect on pentobarbital-appropriate responding produced by pentobarbital.en_US
dc.format.extent293817 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherDrug Discriminationen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherBemegrideen_US
dc.subject.otherPsychiatryen_US
dc.subject.otherPicrotoxinen_US
dc.subject.otherPentylenetetrazolen_US
dc.subject.otherPharmacology/Toxicologyen_US
dc.subject.otherPentobarbitalen_US
dc.subject.otherAntagonismen_US
dc.subject.otherPigeonsen_US
dc.titleSelective blockade of the discriminative stimulus effects of pentobarbital in pigeonsen_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, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartments of Pharmacology and Psychology, University of Michigan, 48109, Ann Arbor, MI, USA; Addiction Research Center, National Institute on Drug Abuse, P. O. Box 12390, 40583, Lexington, KY, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid6798625en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46426/1/213_2004_Article_BF00432447.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00432447en_US
dc.identifier.sourcePsychopharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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