Anxiolytic effects of buspirone and gepirone in the fear-potentiated startle paradigm

Psychopharmacology (Berl). 1988;94(1):8-13. doi: 10.1007/BF00735872.

Abstract

Fear potentiation of the acoustic startle reflex was produced by eliciting startle responses in the presence of a light that had been previously paired with a shock. Buspirone (0.6-5.0 mg/kg) and gepirone (1.25-10.0 mg/kg), but not their common metabolite, 1-PP (0.5-40 mg/kg), produced a dose-dependent reduction of fear-potentiated startle. These doses of buspirone and gepirone slightly increased baseline startle levels. Reduction of fear-potentiated startle appears to involve supraspinal sites of action, since intraventricular but not intrathecal administration of buspirone (200 micrograms) reduced fear-enhanced startle. Both buspirone and gepirone were highly efficacious in this model compared to other animal tests that are used to study anxiolytic compounds.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Anti-Anxiety Agents / administration & dosage
  • Anti-Anxiety Agents / pharmacology*
  • Buspirone / administration & dosage
  • Buspirone / pharmacology*
  • Dose-Response Relationship, Drug
  • Fear / drug effects
  • Injections, Intraventricular
  • Injections, Spinal
  • Male
  • Pyrimidines / administration & dosage
  • Pyrimidines / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Reflex, Startle / drug effects*

Substances

  • Anti-Anxiety Agents
  • Pyrimidines
  • gepirone
  • Buspirone