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Narcotic discrimination in pigeons: Antagonism by naltrexone

dc.contributor.authorHerling, Seymoreen_US
dc.contributor.authorValentino, Rita J.en_US
dc.contributor.authorSolomon, Robert E.en_US
dc.contributor.authorWoods, James H.en_US
dc.date.accessioned2006-04-07T18:18:52Z
dc.date.available2006-04-07T18:18:52Z
dc.date.issued1984-10-01en_US
dc.identifier.citationHerling, Seymore, Valentino, Rita J., Solomon, Robert E., Woods, James H. (1984/10/01)."Narcotic discrimination in pigeons: Antagonism by naltrexone." European Journal of Pharmacology 105(1-2): 137-142. <http://hdl.handle.net/2027.42/24677>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T1J-479DV0C-K3/2/5d056bc40c351af920073d3a520ceb8aen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/24677
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6386494&dopt=citationen_US
dc.description.abstractIn pigeons trained to discriminate between morphine (10 mg/kg) and saline, both morphine and ethylketazocine produced dose-related morphine-appropriate responding. The maximum effect produced by meperidine, however, was only 60% of that produced by morphine or ethylketazocine. Naltrexone (0.1-1.0 mg/kg) produced dose-related shifts to the right in the dose-response curves for the discriminative stimulus and rate-decreasing effects of morphine and ethylketazocine without affecting the response produced by meperidine. Thus, in contrast to the effects observed in other species, morphine and ethylketazocine produce similar discriminative effects in the pigeon. In addition, the morphine-like discriminative effects and the rate-decreasing effects of meperidine in the pigeon are not mediated by the naltrexone-sensitive mechanisms which mediate these effects of morphine or ethylketazocine.en_US
dc.format.extent413886 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleNarcotic discrimination in pigeons: Antagonism by naltrexoneen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Pharmacology and Psychology, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.; Clinical Institute, Addiction Research Foundation, Toronto, Ontario, Canadaen_US
dc.contributor.affiliationumDepartments of Pharmacology and Psychology, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.; Clinical Institute, Addiction Research Foundation, Toronto, Ontario, Canadaen_US
dc.contributor.affiliationumDepartments of Pharmacology and Psychology, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.; Clinical Institute, Addiction Research Foundation, Toronto, Ontario, Canadaen_US
dc.contributor.affiliationumDepartments of Pharmacology and Psychology, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.; Clinical Institute, Addiction Research Foundation, Toronto, Ontario, Canadaen_US
dc.identifier.pmid6386494en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/24677/1/0000096.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0014-2999(84)90657-5en_US
dc.identifier.sourceEuropean Journal of Pharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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