Increased cortical nitric oxide release after phencyclidine administration

Synapse - Tập 63 Số 12 - Trang 1083-1088 - 2009
Erik Pålsson1,2,3, Niall J. Finnerty1,3, Kim Fejgin2,3, Daniel Klamer2, Caroline Wass4, Lennart Svensson2, John Lowry1
1Department of Chemistry, National University of Ireland Maynooth, Maynooth, Ireland
2Department of Pharmacology, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Göteborg, Sweden
3Erik Pålsson, Niall Finnerty, and Kim Fejgin contributed equally to this work.
4Forensic Psychiatry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden

Tóm tắt

Abstract

Phencyclidine exerts psychotomimetic effects in humans and is used as a pharmacological animal model for schizophrenia. We, and others, have demonstrated that phencyclidine induces cognitive deficits in rats that are associated with schizophrenia. These cognitive deficits can be normalized by inhibition of nitric oxide synthase. The development of selective microelectrochemical nitric oxide sensors may provide direct evidence for the involvement of nitric oxide in these effects. The aim of the present study was to use LIVE (long term in vivo electrochemistry) to investigate the effect of phencyclidine, alone or in combination with the nitric oxide synthase inhibitor L‐NAME, on nitric oxide levels in the medial prefrontal cortex of freely moving rats. Phencyclidine (2 mg kg−1) produced an increase in cortical nitric oxide levels and this increase was ameliorated by L‐NAME (10 mg kg−1). Tentatively, the results from the present study provide a biochemical rationale for the involvement of nitric oxide in the phencyclidine model of schizophrenia. Synapse 63:1083–1088, 2009. © 2009 Wiley‐Liss, Inc.

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