Nitric oxide synthase inhibitors improve prepulse inhibition responses of Wistar rats

Author(s)

Issy, A. C. ^{[1, 2]} ; Lazzarini, M. ^{[2, 3]} ; Szawka, R. E. ^[4] ; Carolina, R. O. G. ^[2] ; Anselmo-Franci, J. A. ^[2] ; Del Bel, E. A. ^[2]

Affiliation

^[1] Univ Sao Paulo, FMRP, Dept Pharmacol, BR-14049900 Ribeirao Preto, SP - Brazil

^[2] Univ Sao Paulo, FORP, Dept MEF Physiol, BR-14040904 Ribeirao Preto, SP - Brazil

^[3] Univ Sao Paulo, Dept Neurol Psychiat & Med Psychol, FMRP, BR-14049900 Ribeirao Preto, SP - Brazil

^[4] Univ Fed Minas Gerais, Dept Phys & Biophys, Inst Biol Sci, BR-31270910 Belo Horizonte, MG - Brazil

• Document type: Journal article
• Source: Behavioural Brain Research; v. 217, n. 2, p. 416-423, MAR 1 2011.
• Web of Science Citations: 8

Abstract

Introduction: Cognitive and attentional deficits in schizophrenia include impairment of the sensorimotor filter as measured by prepulse inhibition (PPI). In this way, the study of animals that naturally present low PPI responses could be a useful approach for screening new antipsychotic drugs. Several pieces of evidence suggest that dopamine and nitric oxide (NO) can modulate PPI but their role in those animals is unknown. Objectives: The aim of this study was to investigate the role of dopamine and NO in Wistar rats with naturally low PPI response. Methods: Male Wistar rats with low PPI responses received an i.p. injection of the antipsychotics haloperidol (0.1, 0.3 or 1 mg/kg) or clozapine (0.5, 1.5 or 5 mg/kg), the anxiolytic diazepam (1 or 3 mg/kg) or the NO synthase (NOS) inhibitors, N(G)- nitro-L-arginine (L-NOARG; 40 mg/kg, acutely or sub-chronically) or 7-Nitroindazole (7-NI; 3, 10 or 30 mg/kg). All animals were submitted to the PPI test 1 h after injection. Striatal and cortical dopamine, DOPAC, and noradrenaline levels of rats with low PPI responses were compared to rats with normal PPI responses. Results: We found increased levels of catecholamines on the striatum and prefrontal cortex of Wistar rats with low PPI. In these animals, both antipsychotics, typical and atypical, and NOS inhibitors significantly increased PPI. Conclusion: Taken together, our findings suggest that the low PPI phenotype may be driven by an over-active catecholamine system. Additionally, our results corroborate the hypothesis of dopamine and NO interaction on PPI modulation and suggest that Wistar rats with low PPI may represent an interesting non-pharmacological model to evaluate new potential antipsychotics. (C) 2010 Elsevier B.V. All rights reserved. (AU)