4.0 Article Proceedings Paper

Atypical antipsychotics clozapine and quetiapine attenuate prepulse inhibition deficits in dopamine transporter knockout mice

Journal

BEHAVIOURAL PHARMACOLOGY
Volume 19, Issue 5-6, Pages 562-565

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/FBP.0b013e32830dc110

Keywords

antipsychotics; bipolar disorder; clozapine; dopamine transporter; knockout; mouse; prepulse inhibition; quetiapine; schizophrenia

Funding

  1. NIMH NIH HHS [R37 MH042228, P50 MH060451-01A20004, MH60451, P50 MH060451, R01 MH071916, R01 MH071916-05, R01 MH042228-21, MH42228, R01 MH042228, MH071916] Funding Source: Medline
  2. NINDS NIH HHS [NS19576, R01 NS019576, R01 NS019576-24] Funding Source: Medline

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Sensorimotor gating disruptions are seen in various psychiatric illnesses with putatively different pathologies, including schizophrenia and bipolar disorder. Interestingly, mice lacking the dopamine (DA) transporter (DAT) gene display markedly increased levels of DA, deficits in sensorimotor gating, and hyperactivity relative to wild-type mice. Atypical antipsychotics are effective treatments of schizophrenia and manic symptoms, presumably in part by antagonizing DA receptors. Here we report that treatment with clozapine (3 mg/kg) or quetiapine (2.5 mg/kg) attenuated prepulse inhibition deficits in male DAT knockout mice. Thus male DAT knockout mice may provide a useful animal model for predicting the efficacy of novel drugs in treating psychiatric illnesses characterized by a dysregulated DA system.

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