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Naloxone enhancement of DMT and LSD-25 induced suppression of food-rewarded bar pressing behavior in the rat

dc.contributor.authorDomino, Edward F.en_US
dc.contributor.authorDemetriou, Sandraen_US
dc.contributor.authorKovacic, Beverlyen_US
dc.contributor.authorRuffing, Diane M.en_US
dc.date.accessioned2006-09-11T17:44:50Z
dc.date.available2006-09-11T17:44:50Z
dc.date.issued1979-01en_US
dc.identifier.citationRuffing, Diane; Kovacic, Beverly; Demetriou, Sandra; Domino, Edward F.; (1979). "Naloxone enhancement of DMT and LSD-25 induced suppression of food-rewarded bar pressing behavior in the rat." Psychopharmacology 62(3): 207-210. <http://hdl.handle.net/2027.42/46408>en_US
dc.identifier.issn0033-3158en_US
dc.identifier.issn1432-2072en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46408
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=111285&dopt=citationen_US
dc.description.abstractThe narcotic antagonist naloxone was tested to determine its possible interaction with N,N-dimethyltryptamine (DMT) and lysergic acid diethylamide-25 (LSD) in adult male Holtzman rats trained to press a bar on a fixed-ratio four schedule (FR 4 ), i.e., every fourth press earned a reward of 0.01 ml sugar sweetened milk. LSD (0.1 mg/kg) or increasing doses of DMT (1.0, 3.2, and 10.0 mg/kg) were administered i.p. to disrupt food-rewarded fixed ratio bar pressing in a dose related fashion. Pretreatment (5–10 min) with behaviorally ineffective doses of naloxone (1.0–5.6 mg/kg) dramatically enhanced the effects of DMT and LSD. The content of DMT in the brain and liver of rats injected with DMT alone (10 mg/kg) and with a 5 min pretreatment of naloxone (3.2 mg/kg) was determined by radiochemical analysis at 30 and 90 min after 14 C-DMT injection. There was no significant difference for either brain or liver 14 C-DMT levels when control DMT rats were compared with the naloxone pretreated rats. These results seem to rule out interference by naloxone with the metabolism of DMT as a mechanism of the observed behavioral potentiation.en_US
dc.format.extent397220 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherLSDen_US
dc.subject.otherLiveren_US
dc.subject.otherRaten_US
dc.subject.otherPsychiatryen_US
dc.subject.otherPharmacology/Toxicologyen_US
dc.subject.otherNaloxoneen_US
dc.subject.otherPotentiationen_US
dc.subject.otherDMTen_US
dc.subject.otherFR 4 Operant Behavioren_US
dc.subject.otherBrainen_US
dc.titleNaloxone enhancement of DMT and LSD-25 induced suppression of food-rewarded bar pressing behavior in the raten_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, Lafayette Clinic, 951 E. Lafayette, 48207, Detroit, Michigan, USA; The University of Michigan, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pharmacology, Lafayette Clinic, 951 E. Lafayette, 48207, Detroit, Michigan, USA; The University of Michigan, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pharmacology, Lafayette Clinic, 951 E. Lafayette, 48207, Detroit, Michigan, USA; The University of Michigan, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pharmacology, Lafayette Clinic, 951 E. Lafayette, 48207, Detroit, Michigan, USA; The University of Michigan, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid111285en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46408/1/213_2004_Article_BF00431949.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00431949en_US
dc.identifier.sourcePsychopharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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