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dc.contributor.authorDunn, Michael
dc.contributor.authorKillcross, Simon
dc.date.accessioned2008-10-17T11:25:32Z
dc.date.available2008-10-17T11:25:32Z
dc.date.issued2007-06-01en_UK
dc.identifier.citation(2007) Psychopharmacology 192 (3), pp.347-355en_UK
dc.identifier.issn0033-3158en_UK
dc.identifier.urihttp://hdl.handle.net/10369/320
dc.description.abstractIt has been argued that tasks that necessitate the use of context in the service of goal-directed behaviour are disrupted in both schizophrenic patients and in animal analogues by dopamine (DA) manipulation with the prefrontal cortex being implicated. Objectives To determine the effects on conditional discrimination performance of direct infusion of the DA D1/D2 receptor antagonist α-flupenthixol into the medial prefrontal cortex (mPFC) and of its reversal potential on d-amphetamine-induced task disruption. Materials and methods Conditional discrimination performance in which rats learn to respond on an appropriate lever, conditional upon specific auditory stimuli, was acquired and later tested under the above drug treatment protocol in extinction. Results Conditional discrimination performance was unaffected by bilateral intra-mPFC α-flupenthixol at doses of 12, 24 or 36 μg/μl. A dose of d-amphetamine (1.5 mg/kg) shown previously to disrupt conditional discrimination performance was attenuated by direct PFC infusion of α-flupenthixol at doses of 24 and 36 but not 12 μg/μl per site. Conclusions These results show that conditional discrimination performance is at least in part mediated by prefrontal DA as local PFC DA antagonism attenuates task performance disruption by the indirect DA agonist d-amphetamine further implicating the role of dysfunctional forebrain DA in cognitive deficits evident in schizophrenia.
dc.publisherSpringeren_UK
dc.relation.ispartofseriesPsychopharmacologyen_UK
dc.titleMedial prefrontal cortex infusion of alpha-flupenthixol attenuates systemic d-amphetamine-induced disruption of conditional discrimination performance in ratsen_UK
dc.identifier.doihttp://dx.doi.org/10.1007/s00213-007-0714-2en_UK


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