Modulation of the GABAA receptor by progesterone metabolites

Proc R Soc Lond B Biol Sci. 1987 Aug 21;231(1264):359-69. doi: 10.1098/rspb.1987.0049.


The naturally occurring progesterone metabolites 5 beta-pregnan-3 alpha-ol-20-one and 5 beta-pregnane-3,20-dione reversibly enhance membrane currents elicited by locally applied GABA in bovine adrenomedullary chromaffin cells. Such potentiation was not influenced by the benzodiazepine antagonist Ro 15-1788. At concentrations in excess of those necessary to evoke potentiation of GABA currents, 5 beta-pregnan-3 alpha-ol-20-one and 5 beta-pregane-3,20-dione directly activated a membrane conductance. The resulting currents were potentiated by phenobarbitone and diazepam, and abolished by the GABAA-receptor antagonist, bicuculline. On outside-out membrane patches, 5 beta-pregnan-3 alpha-ol-20-one and 5 beta-pregnane-3,20-dione activated single channel currents of similar amplitude to those evoked by GABA. The results suggest that certain naturally occurring steroids potentiate the actions of GABA and, additionally, directly activate the GABAA receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Medulla / drug effects
  • Adrenal Medulla / physiology*
  • Animals
  • Cattle
  • Cells, Cultured
  • Kinetics
  • Membrane Potentials / drug effects
  • Phenobarbital / pharmacology
  • Pregnanediones / pharmacology*
  • Pregnanes / pharmacology*
  • Pregnanolone / pharmacology*
  • Receptors, GABA-A / drug effects
  • Receptors, GABA-A / physiology*
  • gamma-Aminobutyric Acid / pharmacology*


  • Pregnanediones
  • Pregnanes
  • Receptors, GABA-A
  • gamma-Aminobutyric Acid
  • Pregnanolone
  • Phenobarbital