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Naloxone blockade of amphetamine place preference conditioning

dc.contributor.authorBelluzzi, James D.en_US
dc.contributor.authorTrujillo, Keith A.en_US
dc.contributor.authorStein, Larryen_US
dc.date.accessioned2006-09-11T17:39:25Z
dc.date.available2006-09-11T17:39:25Z
dc.date.issued1991-06en_US
dc.identifier.citationTrujillo, Keith A.; Belluzzi, James D.; Stein, Larry; (1991). "Naloxone blockade of amphetamine place preference conditioning." Psychopharmacology 104(2): 265-274. <http://hdl.handle.net/2027.42/46337>en_US
dc.identifier.issn1432-2072en_US
dc.identifier.issn0033-3158en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46337
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1876671&dopt=citationen_US
dc.description.abstractAmphetamine and naloxone were examined in place conditioning, in order to study possible interactions between endogenous opioids and catecholamines in reinforcement. After initial preferences were determined, animals were conditioned with amphetamine alone (1.0 mg/kg SC), naloxone alone (0.02, 0.2 or 2.0 mg/kg SC) or combinations of amphetamine plus naloxone. A reliable, long-lasting preference for the compartment associated with amphetamine was observed, reflecting the reinforcing properties of this drug. No preference or aversion was observed in animals that received saline in both compartments. Naloxone (0.02, 0.2 and 2.0 mg/kg) produced a dose-dependent place aversion; while the lowest dose had effects similar to saline, the higher doses produced significant place aversions. Naloxone, at all three doses examined, prevented the ability of amphetamine to produce a place preference. Thus, the lowest dose of naloxone, having no effects alone in place conditioning was still able to block the reinforcing effects of amphetamine. These results suggest that the reinforcing effects of amphetamine are dependent on activation of opiate receptors, and provide further evidence that interactions between endogenous opioids and catecholamines may be important in reinforcement.en_US
dc.format.extent1646433 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherPharmacology/Toxicologyen_US
dc.subject.otherReinforcementen_US
dc.subject.otherD -Amphetamineen_US
dc.subject.otherPlace Conditioningen_US
dc.subject.otherEndogenous Opioidsen_US
dc.subject.otherRewarden_US
dc.subject.otherBiomedicineen_US
dc.subject.otherPsychiatryen_US
dc.subject.otherNaloxoneen_US
dc.subject.otherConditioned Place Preferenceen_US
dc.subject.otherCatecholaminesen_US
dc.titleNaloxone blockade of amphetamine place preference conditioningen_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.affiliationumDepartment of Pharmacology, University of California, 92717, Irvine, CA, USA; Mental Health Research Institute, The University of Michigan, 205 Washtenaw Place, 48109-0720, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherDepartment of Pharmacology, University of California, 92717, Irvine, CA, USAen_US
dc.contributor.affiliationotherDepartment of Pharmacology, University of California, 92717, Irvine, CA, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid1876671en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46337/1/213_2005_Article_BF02244190.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF02244190en_US
dc.identifier.sourcePsychopharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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