Constriction of mouse hepatic venules and sinusoids by endothelins through ETB receptor subtype

Int J Microcirc Clin Exp. 1996 Sep-Oct;16(5):250-8. doi: 10.1159/000179181.

Abstract

Objective: This study was conducted to examine the effects of endothelin (ET)-1 and ET-3 on hepatic venules and sinusoids and to identify the subtypes of ET receptors.

Method: Hepatic venules and sinusoids of anesthetized mice were observed at the edge of the liver. ET-1, ET-3 and sarafotoxin (S6c, a selective ETB receptor agonist) were applied topically over the microvasculature.

Results: ET-1, ET-3 and S6c (1-100 microM, 30 microliters) induced dose-dependent vasoconstriction of the portal venules, the sinusoids and the central venules. The ETs and S6c were equipotent for these microvessels. BQ-123 (a selective ETA receptor antagonist) inhibited the constrictive effects of ET-3 (not of ET-1) on the portal venules and central venules, whereas it had no inhibitory effect on the sinusoids.

Conclusions: In mouse hepatic venules and sinusoids, the vasoconstriction induced by ET-1 and ET-3 was mediated mainly through the ETB receptor subtype and partly through an unknown BQ-123-sensitive ET receptor subtype in the portal and central venules, and only through the ETB receptor subtype in the sinusoids.

MeSH terms

  • Animals
  • Endothelin-1 / pharmacology*
  • Endothelin-3 / pharmacology*
  • Liver / blood supply*
  • Male
  • Mice
  • Receptor, Endothelin B
  • Receptors, Endothelin / agonists
  • Receptors, Endothelin / physiology*
  • Vasoconstriction / drug effects*
  • Vasoconstrictor Agents / pharmacology
  • Venules / drug effects
  • Venules / physiology
  • Viper Venoms / pharmacology

Substances

  • Endothelin-1
  • Endothelin-3
  • Receptor, Endothelin B
  • Receptors, Endothelin
  • Vasoconstrictor Agents
  • Viper Venoms
  • sarafotoxins s6