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Activation of a nitric-oxide-sensitive cAMP pathway with phencyclidine: elevated hippocampal cAMP levels are temporally associated with deficits in prepulse inhibition

Journal article
Authors Daniel Klamer
Erik Pålsson
Kim Fejgin
J. Zhang
Jörgen Engel
Lennart Svensson
Published in Psychopharmacology (Berl)
Volume 179
Issue 2
Pages 479-88
Publication year 2005
Published at Institute of Physiology and Pharmacology, Dept of Pharmacology
Pages 479-88
Language en
Keywords Acoustic Stimulation, Animals, Cyclic AMP/*physiology, Enzyme Inhibitors/pharmacology, Excitatory Amino Acid Antagonists/*pharmacology, Hippocampus/*drug effects/*metabolism, Male, Microdialysis, NG-Nitroarginine Methyl Ester/pharmacology, Nerve Tissue Proteins/antagonists & inhibitors, Nitric Oxide/*physiology, Nitric Oxide Synthase/antagonists & inhibitors, Nitric Oxide Synthase Type I, Phencyclidine/*pharmacology, Radioimmunoassay, Rats, Rats, Sprague-Dawley, Startle Reaction/*drug effects
Subject categories Physiology


RATIONALE: Schizophrenic patients show deficits in pre-attentive information processing as evidenced, for example, by disrupted prepulse inhibition, a measure of sensorimotor gating. A similar disruption can be observed in animals treated with the psychotomimetic agent, phencyclidine (PCP). However, the mechanism by which PCP alters brain function has not been fully elucidated. Recent studies have demonstrated that certain behavioural and neurochemical effects of PCP in rats and mice are blocked by nitric oxide (NO) synthase inhibition, suggesting an important role for NO in the effects of PCP. OBJECTIVE: The aim of the present study was to investigate the effects of PCP on cAMP production in the ventral hippocampus and the role of NO in these effects using in vivo microdialysis in rats. Furthermore, the effects of PCP on acoustic startle reactivity and prepulse inhibition of acoustic startle were compared with changes in cAMP levels in the ventral hippocampus. RESULTS: Significant increases in cAMP levels were observed in the ventral hippocampus following both local infusion (10(-4) mol/l and 10(-3) mol/l) and systemic administration (2 mg/kg) of PCP. The PCP-induced changes in prepulse inhibition and startle reactivity were associated in magnitude and duration with the increase in cAMP levels in the hippocampus. Furthermore, systemic administration of the NO synthase inhibitor, L: -NAME (10 mg/kg), blocked both the changes in cAMP levels and the behavioural responses induced by PCP. CONCLUSIONS: These findings indicate that the effects of PCP on prepulse inhibition and startle reactivity are associated with an increase in cAMP levels in the ventral hippocampus, and that this change in cAMP response may be linked to the production of NO.

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