Relaxation of human coronary artery and arteria mammaria by K(+)-channel openers

J Cardiovasc Pharmacol. 1992:20 Suppl 3:S13-6. doi: 10.1097/00005344-199206203-00004.

Abstract

Three agents with K(+)-channel-opening activity--nicorandil, bimakalim (EMD 52692), and EMD 56431--were tested for vasorelaxation abilities in human coronary artery and human arteria mammaria. The potency orders were bimakalim = EMD 56431 >> nicorandil for relaxation in human coronary artery and bimakalim = EMD 56431 >> nicorandil in human arteria mammaria. These data demonstrate that K(+)-channel openers are effective vasorelaxant agents in human coronary artery and human arteria mammaria. Bimakalim and EMD 56431 were more potent than nicorandil, a drug that also activates guanylate cyclase.

MeSH terms

  • Benzopyrans / pharmacology*
  • Coronary Vessels / drug effects*
  • Dihydropyridines / pharmacology*
  • Humans
  • In Vitro Techniques
  • Mammary Arteries / drug effects*
  • Niacinamide / analogs & derivatives*
  • Niacinamide / pharmacology
  • Nicorandil
  • Potassium Channels / drug effects*
  • Vasodilation / drug effects
  • Vasodilator Agents / pharmacology*

Substances

  • Benzopyrans
  • Dihydropyridines
  • Potassium Channels
  • Vasodilator Agents
  • Niacinamide
  • Nicorandil
  • bimakalim