Modulation of GABAA and glycine receptors by chlormethiazole

Eur J Pharmacol. 1992 Jan 21;210(3):239-46. doi: 10.1016/0014-2999(92)90410-6.

Abstract

The influence of chlormethiazole, on currents evoked by gamma-aminobutyric acid (GABA) and glycine, was investigated under voltage-clamp conditions, in bovine chromaffin cells and murine spinal neurones, respectively. Chlormethiazole (30 and 100 microM) dose dependently potentiated currents activated by either inhibitory neurotransmitter. The potentiation of the GABA-evoked response occurred without altering the reversal potential and was not influenced by the benzodiazepine receptor antagonist Ro 15-1788 (300 nM). GABA-gated channels, recorded from outside-out membrane patches, showed increased probability of being in the conducting state in the presence of chlormethiazole. High concentrations of chlormethiazole (3 mM) activated bicuculline (1 microM)-sensitive whole-cell currents with a reversal potential similar to the chloride equilibrium potential. Chlormethiazole potentiates GABA- and glycine-activated currents and at higher doses, directly activates the GABAA receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cells, Cultured
  • Chlormethiazole / pharmacology*
  • Chromaffin System / drug effects
  • Drug Synergism
  • Electric Stimulation
  • Electrophysiology
  • Glycine / pharmacology
  • Mice
  • Neurons / drug effects
  • Receptors, GABA-A / drug effects*
  • Receptors, GABA-A / physiology
  • gamma-Aminobutyric Acid / pharmacology

Substances

  • Receptors, GABA-A
  • Chlormethiazole
  • gamma-Aminobutyric Acid
  • Glycine