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Behavioural observations in gunn rats

dc.contributor.authorZand, Roberten_US
dc.contributor.authorIzquierdo, Ivánen_US
dc.date.accessioned2006-09-11T17:44:29Z
dc.date.available2006-09-11T17:44:29Z
dc.date.issued1978-01en_US
dc.identifier.citationIzquierdo, Iván; Zand, Robert; (1978). "Behavioural observations in gunn rats." Psychopharmacology 57(2): 155-161. <http://hdl.handle.net/2027.42/46403>en_US
dc.identifier.issn1432-2072en_US
dc.identifier.issn0033-3158en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46403
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=418449&dopt=citationen_US
dc.description.abstractThe Gunn rat is a hooded mutant of albino rat with various biochemical defects, including a low UDP-glucuronosyl-transferase activity. As a consequence, about half of their offspring are jaundiced from birth, due to high free bilirubin levels, and develop widespread brain damage. The behaviour of both jaundiced and nonjaundiced Gunn rats was studied in four different tests in a shuttle-box and in a stepthrough passive avoidance situation, and compared with that of normal hooded rats. No differences among groups were found in performance of shuttle responses to a tone in a pseudoconditioning paradigm in which tones and shocks were given at random. However, rats from the two Gunn groups made less shuttlings to the tone in two tests that involved an avoidance contingency (each response cancelled one shock). In addition, nonicteric Gunn rats also performed poorly in a classical conditioning test in the shuttle-box (tones and shocks paired on every trial regardless of responses). This last deficiency of non-icteric Gunn rats may be explained by their higher tendency to freeze in situations involving stimulus-stimulus interactions. They also showed a higher latency than that of the two other groups to enter the dark side of the step-through apparatus on their first exposure to it. All animals seemed to learn the passive-avoidance task to the same extent, however, as shown in a retest carried out 48 h later. Both Gunn groups were hypersensitive to the stereotyped-behaviour-inducing action of apomorphine (0.125–1.0 mg/kg, i.p.), but all groups were about equally sensitive to that of d -amphetamine sulfate (0.5–4.0 mg/kg). Since apomorphine is disposed of by glucuronidation, this might be explained by the low UDP-glucuronosyl-transferase activity known to exist in the Gunn animals. The present results show that additional genetic defects have developed by in-breeding in the Gunn population, which are unrelated to brain damage caused by bilirubin, and which can be well characterized from a behavioural standpoint.en_US
dc.format.extent747414 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.otherD -Amphetamineen_US
dc.subject.otherStereotyped Behaviouren_US
dc.subject.otherClassical Conditioningen_US
dc.subject.otherActive Avoidanceen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherPsychiatryen_US
dc.subject.otherGunn Ratsen_US
dc.subject.otherShuttle Behaviouren_US
dc.subject.otherPassive Avoidanceen_US
dc.subject.otherPseudoconditioningen_US
dc.subject.otherApomorphineen_US
dc.titleBehavioural observations in gunn ratsen_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.affiliationumBiophysics Research Division, Institute of Science and Technology, University of Michigan, 48105, Ann Arbor, Michigan, USA; Dept. Biofisica e Fisiologia, Escola Paulista de Medicina, Rua Botucatu 862, 04023, São Paulo, SP, Brasilen_US
dc.contributor.affiliationumBiophysics Research Division, Institute of Science and Technology, University of Michigan, 48105, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid418449en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46403/1/213_2004_Article_BF00426881.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00426881en_US
dc.identifier.sourcePsychopharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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