Neurosteroid analogues. 12. Potent enhancement of GABA-mediated chloride currents at GABAA receptors by ent-androgens

Eur J Med Chem. 2008 Jan;43(1):107-13. doi: 10.1016/j.ejmech.2007.02.017. Epub 2007 Mar 12.

Abstract

Allopregnanolone (1) and pregnanolone (2), steroids containing a 17beta-acetyl group, are potent enhancers of GABA (gamma-aminobutyric acid) action at GABAA receptors. Their effects are enantioselective with the non-naturally occurring enantiomers (ent-1 and ent-2) being less potent. Androsterone (3) and etiocholanolone (4), steroids with a C-17 carbonyl group, are weak enhancers of GABA action at GABAA receptors. Unexpectedly, their enantiomers (ent-3 and ent-4) have been found to have enhanced, not diminished, activity at GABAA receptors. Furthermore, the C-17 spiro-epoxide analogues (ent-5 and ent-6) of ent-3 and ent-4, respectively, have activities comparable to those of steroids 1 and 2. The results indicate that some ent-steroids are potent modulators of GABAA receptors and might have clinical potential as GABAergic drugs of the future.

Publication types

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

MeSH terms

  • Androgens / chemistry*
  • Androgens / metabolism
  • Androgens / pharmacology*
  • Animals
  • Bridged Bicyclo Compounds, Heterocyclic / antagonists & inhibitors
  • Bridged Bicyclo Compounds, Heterocyclic / metabolism
  • Chloride Channels / metabolism*
  • GABA Modulators / chemistry*
  • GABA Modulators / metabolism
  • GABA Modulators / pharmacology*
  • Larva / drug effects
  • Larva / physiology
  • Rats
  • Receptors, GABA-A / metabolism*
  • Stereoisomerism
  • Steroids / chemistry*
  • Steroids / metabolism
  • Steroids / pharmacology*

Substances

  • Androgens
  • Bridged Bicyclo Compounds, Heterocyclic
  • Chloride Channels
  • GABA Modulators
  • Receptors, GABA-A
  • Steroids
  • tert-butylbicyclophosphorothionate