AI Article Synopsis

  • The study investigates how the drug phencyclidine (PCP) affects prepulse inhibition, a measure of sensorimotor gating, in mice lacking neuronal nitric oxide synthase (nNOS).
  • PCP significantly increases prepulse inhibition in nNOS-deficient mice, while it does not affect the prepulse inhibition in nNOS-normal mice, indicating a potential role of nNOS in this behavioral response.
  • The findings suggest that nNOS contributes to the nitric oxide-sensitive effects of PCP, as it also influences startle response reactivity differently across the various genotypes of the mice.

Article Abstract

Prepulse inhibition of acoustic startle is a behavioural response, which is used to estimate sensorimotor gating deficits in schizophrenia. Recent studies show that several behavioural effects of the psychotomimetic drug, phencyclidine (PCP), in rodents are blocked by nitric oxide synthase (NOS) inhibitors suggesting that NO plays an important role in the pharmacological effects of PCP. The present study was conducted to examine the effects of PCP on prepulse inhibition in neuronal NOS (nNOS) deficient mice. PCP treatment caused a significant and dose-related increase in prepulse inhibition in nNOS-/- mice whereas prepulse inhibition was not significantly affected in +/+ and +/- mice. Basal prepulse inhibition level did not differ significantly between the groups. Furthermore, PCP caused a dose-related decrease in startle response reactivity in +/+ mice but did not significantly affect this measure in +/- and -/- mice. Basal startle response level did not differ between +/+ and +/- but was significantly lower in -/- mice. It is concluded that nNOS plays a role in the NO-sensitive effects of PCP.

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Source
http://dx.doi.org/10.1016/j.euroneuro.2005.02.002DOI Listing

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