Nitric oxide synthase inhibitors produce phencyclidine-like behavioral effects in pigeons

David C. Jewett, Eduardo R. Butelman, James H. Woods

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

The present study assessed the ability of nitric oxide synthase (NOS) inhibitors to produce PCP-like behavioral effects in pigeons. Food-restricted pigeons were trained to discriminate between PCP (1.0 mg/kg, i.m.) from saline in a two-key operant procedure. NOS inhibitors 7-nitroindazole (7-NI) and N(ω)-nitro-L-arginine methyl ester (L-NAME) produced PCP-like discriminative stimulus effects. 7-NI (17.8 mg/kg, i.m.) completely generalized to PCP. L-NAME (320-1000 mg/kg) produced partial generalization to PCP. D-NAME, the enantiomer of L-NAME, did not produce PCP-appropriate behavior. L-NAME was approximately 200-times more potent i.c.v., but did not fully generalize to PCP. Both NOS inhibitors were effective in producing catalepsy, which is an effect commonly produced by competitive and uncompetitive NMDA antagonists. 7-NI (32 mg/kg) produced catalepsy in all subjects, whereas L-NAME (3200 mg/kg) produced catalepsy in 50% of the subjects. D-NAME did not produce catalepsy. Pretreatment with L-arginine (32-3200 mg/kg) prevented the PCP-like discriminative stimulus and cataleptic effects of 7-NI (17.8-32 mg/kg), demonstrating that 7-NI produced PCP-like effects through blockade of NO synthesis. The current studies reveal that NOS inhibitors induced two behavioral actions, discriminative stimulus effects and catalepsy, that are very selective for NMDA antagonists in pigeons.

Original languageEnglish (US)
Pages (from-to)25-31
Number of pages7
JournalBrain Research
Volume715
Issue number1-2
DOIs
StatePublished - Apr 9 1996
Externally publishedYes

Keywords

  • 7-nitroindazole
  • catalepsy
  • discriminative stimulus
  • drug discrimination
  • N(ω)-nitro-L-arginine methyl ester
  • nitric oxide
  • operant behavior
  • phencyclidine

ASJC Scopus subject areas

  • Neuroscience(all)
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

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