Altered response to benzodiazepine anxiolytics in mice lacking GABA B(1) receptors

Eur J Pharmacol. 2004 Aug 16;497(1):119-20. doi: 10.1016/j.ejphar.2004.06.036.

Abstract

Recently, we demonstrated that mice lacking the GABA(B(1)) subunit were more anxious than wild-type animals in several behavioural paradigms, most notably in the light-dark test. In an attempt to assess the effects of classical benzodiazepine anxiolytics on anxiety-like behaviour observed in these mice, animals were administered either chlordiazepoxide (10 mg/kg, p.o.) or diazepam (7.5 mg/kg, p.o.) prior to testing in the light-dark box. Surprisingly, in contrast with the wild-type mice, neither benzodiazepines decreased anxiety-like behaviour in GABA(B(1))(-/-) mice. These data suggest that targeted deletion of GABA(B(1)) subunit alters GABA(A) receptor function in vivo.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Anti-Anxiety Agents / pharmacology*
  • Anti-Anxiety Agents / therapeutic use
  • Anxiety / drug therapy
  • Anxiety / genetics
  • Anxiety / psychology
  • Chlordiazepoxide / pharmacology*
  • Chlordiazepoxide / therapeutic use
  • Diazepam / pharmacology*
  • Diazepam / therapeutic use
  • Female
  • Male
  • Mice
  • Mice, Knockout
  • Motor Activity / drug effects
  • Receptors, GABA-A / physiology
  • Receptors, GABA-B / genetics
  • Receptors, GABA-B / physiology*

Substances

  • Anti-Anxiety Agents
  • Receptors, GABA-A
  • Receptors, GABA-B
  • Chlordiazepoxide
  • Diazepam