Inhibition of neuronal nitric oxide reduces anxiety-like responses to pair housing

Joanna L. Workman, Brian C. Trainor, M. Sima Finy, Randy J. Nelson

Research output: Contribution to journalArticle

28 Scopus citations

Abstract

Many psychological disorders are characterized by anxiety and alterations in social interactions. Recent studies demonstrate that the chemical messenger nitric oxide (NO) can regulate both anxiety and social behaviours. We tested whether an enzyme that produces NO in the brain, neuronal nitric oxide synthase (nNOS), serves as an interface between social interactions and anxiety-like behaviour. Several investigators have observed that mice increase anxiety-like responses in the elevated plus-maze after pair housing. nNOS gene deletion and 3-Bromo-7-Nitroindazole were used to inhibit the production of neuronal NO. Similar to previous studies, pair housing reduced open arm exploration in the elevated plus-maze. Pair housing also increased corticotropin-releasing hormone (CRH) immunoreactive cells in the paraventricular nucleus (PVN) of the hypothalamus. Inhibition of NO production increased open arm exploration in pair-housed mice but decreased open arm exploration in individually housed mice. These results suggest that the effect of nNOS inhibition on anxiety-like responses is context dependent and that behavioural responses to social housing are altered after nNOS inhibition. This research suggests that NO may play an important role in mediating the effect social interactions have on anxiety.

Original languageEnglish (US)
Pages (from-to)109-115
Number of pages7
JournalBehavioural Brain Research
Volume187
Issue number1
DOIs
StatePublished - Feb 11 2008

Keywords

  • Corticotropin-releasing hormone
  • Elevated plus-maze
  • Mice
  • nNOS
  • NOS-1
  • Paraventricular nucleus

ASJC Scopus subject areas

  • Behavioral Neuroscience

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