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Chronic infusion of PCP via osmotic mini-pumps: a new rodent model of cognitive deficit in schizophrenia characterized by impaired attentional set-shifting (ID/ED) performance.

Christian Spang Pedersen, Pascal Goetghebeur, Rebecca Dias

Journal of neuroscience methods December 15, 2009 DOI: 10.1016/j.jneumeth.2009.09.014 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Animal model study Peer reviewed
Population Lister hooded rats
Interventions Phencyclidine (PCP) Modafinil
Dose 15 mg/kg/day for PCP
Duration 14-day infusion, 7-day drug-free recovery, then acute injection testing
Key points Continuous 14-day PCP infusion via osmotic mini-pumps produced a selective deficit at the extra-dimensional shift stage of the ID/ED task, which was reversed by acute modafinil administration.

Abstract

The identification of animal disease-like models for cognitive symptoms in schizophrenia is of central importance to the successful development of pharmacological therapies for psychosis resulting in a functional outcome in patients. Executive function is one of the most severely affected cognitive domains in schizophrenia that remains inadequately treated by existing therapies. The rat attentional set-shifting (or intra-dimensional-extra-dimensional (ID/ED)) task has been developed to test executive function in rodents and successful translation of pre-clinical data into the clinical setting now depends on the identification of a predictive animal disease-like model. The present study investigates whether a continuous 14-day mini-pump infusion of the non-competitive NMDA receptor antagonist phencyclidine (PCP) leads to a deficit in the ID/ED task, and subsequently evaluates the effect of modafinil in this model. Lister hooded rats were implanted subcutaneously with osmotic mini-pumps containing saline or PCP (15 mg/kg/day) for 14 days followed by a 7-day drug-free recovery phase. Rats were then tested in the ID/ED task following an acute injection of either vehicle or modafinil. PCP-treated animals displayed a selective deficit at the ED shift stage resembling that observed in schizophrenic patients. This deficit was reversed by an acute injection of modafinil. The PCP-induced impairment and its reinstatement by modafinil are quantitatively and qualitatively similar to that described earlier by our group following sub-chronic intraperitoneal PCP administration, indicative that sub-chronic PCP infusion via osmotic mini-pumps may represent an attractive alternative to the systemic administration protocols generally employed to date.