Psychopharmacology

, Volume 115, Issue 1, pp 167–172

Nitrous oxide anxiolytic effect in mice in the elevated plus maze: Mediation by benzodiazepine receptors

  • D. E. Emmanouil
  • C. H. Johnson
  • R. M. Quock
Original Investigations

DOI: 10.1007/BF02244768

Cite this article as:
Emmanouil, D.E., Johnson, C.H. & Quock, R.M. Psychopharmacology (1994) 115: 167. doi:10.1007/BF02244768

Abstract

In earlier research, we have hypothesized that exposure to nitrous oxide (N2O) produces an anxiolytic effect that is mediated by benzodiazepine (BZ) receptors. The present research was conducted to characterize pharmacologically the behavioral effects of N2O in comparison with a BZ standard, chlordiazepoxide (CP), in the mouse elevated plus maze. Exposure to increasing levels of N2O produced a concentration-related increase in the percent of total entries into and the percent of total time spent on the open arms, a pattern of response similar to that induced by CP. These effects of N2O and CP were both antagonized by pretreatment with the BZ receptor blocker flumazenil (FLU). In another experiment, mice made tolerant to CP also exhibited a cross-tolerance to N2O. These results support the hypothesis that the anxiolytic effect of N2O is mediated by BZ receptors.

Key words

Nitrous oxide Chlordiazepoxide Flumazenil Benzodiazepine receptors Elevated plus maze Mouse 

Copyright information

© Springer-Verlag 1994

Authors and Affiliations

  • D. E. Emmanouil
    • 2
  • C. H. Johnson
    • 1
  • R. M. Quock
    • 1
  1. 1.Department of Biomedical SciencesUniversity of Illinois College of Medicine at RockfordRockfordUSA
  2. 2.University of Athens Faculty of DentistryAthensGreece

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