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An Acad Bras Cienc ; 90(2): 1659-1663, 2018.
Article in English | MEDLINE | ID: mdl-29898114

ABSTRACT

Clozapine is an antipsychotic that produces serious withdrawal effects in schizophrenic patients. Olfactory deficits are well known as part of negative symptoms, but it is not known whether antipsychotic use and/or withdrawal are implicated. Then, we tested clozapine withdrawal in association with two widely used schizophrenia models: Neonatal immune challenge by Polycitidilic-polyinosinic acid (polyI:C) and ketamine. PolyI:C (or saline) was injected subcutaneously in neonatal period, dose of 5 mg/kg from 2 to 6 Post Natal Days, and ketamine or saline at the dose 25mg/kg intraperitoneally (i.p.), daily for 7 days from 53 to 60 post natal day. Clozapine 10mg/kg (or saline) was administered i.p. from 46 to 60 post natal day. Olfactory discrimination test (sensorial and cognitive deficit) was performed at 61 post natal day, 24h after the last injections. The association of PolyI:C, ketamine and clozapine disrupted Olfactory Discrimination, equating time in familiar and non-familiar compartments. PolyI:C plus ketamine increased crossings between compartments. It was produced, for the first time, an olfactory deficit induced by clozapine withdrawal in Wistar rats subjected to schizophrenia animal models.


Subject(s)
Antipsychotic Agents/adverse effects , Clozapine/adverse effects , Olfaction Disorders/chemically induced , Schizophrenia/chemically induced , Substance Withdrawal Syndrome , Animals , Disease Models, Animal , Drug Therapy, Combination/methods , Ketamine/adverse effects , Male , Neuropsychological Tests , Olfaction Disorders/diagnosis , Poly I-C/adverse effects , Preliminary Data , Rats, Wistar
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