4.4 Article

Neonatal phencyclidine and social isolation in the rat: effects of clozapine on locomotor activity, social recognition, prepulse inhibition, and executive functions deficits

期刊

PSYCHOPHARMACOLOGY
卷 238, 期 2, 页码 517-528

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SPRINGER
DOI: 10.1007/s00213-020-05700-y

关键词

Schizophrenia; Animal models; Neonatal PCP; Social isolation; Locomotor activity; Working memory; Prepulse inhibition; Executive functions; Clozapine

资金

  1. Porsolt SAS

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The study aimed to further characterize behavioral changes in a neonatal PCP and post-weaning social isolation dual-hit rat model and evaluate the effects of chronic clozapine treatment on signs related to schizophrenia. The results showed persistent deficits in locomotor activity and social recognition in the PCP-SI rats, which were ameliorated by chronic clozapine treatment, confirming the predictive validity of this animal model.
Rationale There is a need to develop animal models of schizophrenia-like behaviors that have both construct and predictive validity. Recently, a neonatal phencyclidine (PCP) and post-weaning social isolation dual-hit model was developed; however, its face and predictive validities need to be further investigated. Objective The aims of this study were to extend the characterization of the behavioral changes occurring in the neonatal PCP and post-weaning social isolation dual-hit rat model and to evaluate the effects of chronic treatment with clozapine on signs related to schizophrenia. Methods Male Wistar rat pups were treated with PCP (10 mg/kg s.c.) on postnatal days (PND) 7, 9, and 11. Starting from weaning, neonatal PCP-treated rat pups were socially isolated, while control saline-treated rats were group housed. At adulthood, rats were assessed using behavioral tasks evaluating locomotor activity, social recognition, prepulse inhibition, and reversal learning. Clozapine (3 mg/kg i.p.) was administered daily starting from a week before behavioral tests and until the end of the study. Results Neonatal PCP-treated and post-weaning social isolated (PCP-SI) rats displayed persistent and robust locomotor hyperactivity as well as social recognition impairment. The latter could not be explained by variations in the motivation to interact with a juvenile rat. Weak-to-moderate deficits in prepulse inhibition and reversal learning were also observed. Chronic treatment with clozapine attenuated the observed locomotor hyperactivity and social recognition deficits. Conclusion The PCP-SI model presents enduring and robust deficits (hyperactivity and social recognition impairment) associated with positive symptoms and cognitive/social deficits of schizophrenia, respectively. These deficits are normalized by chronic treatment with clozapine, thereby confirming the predictive validity of this animal model.

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