Object recognition impairment and rescue by a dopamine D2 antagonist in hyperdopaminergic mice

dc.contributor.authorFrança, Arthur S.C.
dc.contributor.authorMuratori, Larissa
dc.contributor.authorNascimento, George Carlos do
dc.contributor.authorPereira, Catia Mendes
dc.contributor.authorRibeiro, Sidarta Tollendal Gomes
dc.contributor.authorSoares, Bruno Lobão
dc.date.accessioned2017-06-02T11:31:54Z
dc.date.available2017-06-02T11:31:54Z
dc.date.issued2016
dc.description.resumoGenetically-modified mice without the dopamine transporter (DAT) are hyperdopaminergic, and serve as models for studies of addiction, mania and hyperactive disorders. Here we investigated the capacity for object recognition in mildly hyperdopaminergic mice heterozygous for DAT (DAT +/-), with synaptic dopaminergic levels situated between those shown by DAT -/- homozygous and wild-type (WT) mice. We used a classical dopamine D2 antagonist, haloperidol, to modulate the levels of dopaminergic transmission in a dose-dependent manner, before or after exploring novel objects. In comparison with WT mice, DAT +/- mice showed a deficit in object recognition upon subsequent testing 24h later. This deficit was compensated by a single 0.05mg/kg haloperidol injection 30min before training. In all mice, a 0.3mg/kg haloperidol injected immediately after training impaired object recognition. The results indicate that a mild enhancement of dopaminergic levels can be detrimental to object recognition, and that this deficit can be rescued by a low dose of a D2 dopamine receptor antagonist. This suggests that novel object recognition is optimal at intermediate levels of D2 receptor activity.pt_BR
dc.identifier.doi10.1016/j.bbr.2016.04.009
dc.identifier.urihttps://repositorio.ufrn.br/jspui/handle/123456789/23367
dc.languageengpt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectDAT-KOpt_BR
dc.subjectDopaminept_BR
dc.subjectHaloperidolpt_BR
dc.subjectHeterozygouspt_BR
dc.subjectObject recognitionpt_BR
dc.titleObject recognition impairment and rescue by a dopamine D2 antagonist in hyperdopaminergic micept_BR
dc.typearticlept_BR

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