Selective and non-selective ET antagonists reveal an ET(A)/ET(B) receptor mediated ET-1-induced antinociceptive effect in PAG area of mice

Life Sci. 1997;61(25):PL 397-401. doi: 10.1016/s0024-3205(97)00988-0.

Abstract

The injection of endothelin-1 (ET-1) (2 pmol) into the dorsolateral periaqueductal gray area (PAG) of mice produces antinociceptive effect as underscored by increases in the latency time for the reaction to a hot plate. Pretreatment of the PAG area with bosentan (10 nmol) (a mixed ET(A)/ET(B) receptor antagonist), FR 139317 (5 nmol) (ET[A] receptor selective antagonist) or BQ-788 (5 nmol) (ET[B] receptor selective antagonist) greatly reduced the antinociceptive effect induced by ET-1. Therefore, ET-1 induces antinociceptive effects via both ET(A)/ET(B) receptors. In addition, since ET-antagonists lowered per se the control reaction time of the mice when administered alone to the PAG area, we would suggest that endogenous ET-1 acting within the PAG area contributes to the suppression of pain.

MeSH terms

  • Analgesics / pharmacology
  • Animals
  • Azepines / pharmacology
  • Bosentan
  • Endothelin Receptor Antagonists
  • Endothelin-1 / antagonists & inhibitors*
  • Endothelin-1 / pharmacology
  • Endothelin-1 / physiology
  • Indoles / pharmacology
  • Male
  • Mice
  • Periaqueductal Gray / drug effects*
  • Periaqueductal Gray / metabolism
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Receptors, Endothelin / physiology*
  • Sulfonamides / pharmacology

Substances

  • Analgesics
  • Azepines
  • Endothelin Receptor Antagonists
  • Endothelin-1
  • Indoles
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Receptors, Endothelin
  • Sulfonamides
  • FR 139317
  • Bosentan