Pinacidil inhibits the ryanodine-sensitive outward current and glibenclamide antagonizes its action in cells from the rabbit portal vein

Br J Pharmacol. 1991 Apr;102(4):788-90. doi: 10.1111/j.1476-5381.1991.tb12252.x.

Abstract

Pinacidil, a potassium-channel opener, inhibited the ryanodine-sensitive oscillatory outward potassium current induced by Ca released from an intracellular store. Glibenclamide, a blocker of the ATP-sensitive K-channel, prevented the action of pinacidil, suggesting the presence of an additional site (to K channels) for the vasodilator actions of pinacidil at which glibenclamide can act as an antagonist.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Animals
  • Calcium / physiology
  • Glyburide / pharmacology*
  • Guanidines / antagonists & inhibitors
  • Guanidines / pharmacology*
  • In Vitro Techniques
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism*
  • Pinacidil
  • Portal Vein / drug effects
  • Portal Vein / metabolism
  • Potassium Channels / drug effects*
  • Rabbits
  • Ryanodine / antagonists & inhibitors*
  • Vasodilator Agents / pharmacology*

Substances

  • Guanidines
  • Potassium Channels
  • Vasodilator Agents
  • Ryanodine
  • Pinacidil
  • Adenosine Triphosphate
  • Glyburide
  • Calcium