Sanguinarine: a positive inotropic alkaloid which inhibits cardiac Na+,K+-ATPase

Eur J Pharmacol. 1979 Dec 20;60(4):373-7. doi: 10.1016/0014-2999(79)90245-0.

Abstract

In isolated, isometrically contracting left guinea pig atria, sanguinarine, a benzophenanthridine alkaloid from the papaveracea Sanguinaria canadensis, produced a concentration-dependent positive inotropic effect. Between 2.3 x 10(-6) M and 6.5 x 10(-5) M, sanguinarine increased contractility by 108% which was comparable to the maximal inotropic effect of ouabain. Within the same concentration range, sanguinarine caused inhibition of Na+,K+-ATPase isolated from guinea pig myocardium. 100% inhibition of Na+,K+,ATPase activity occurred at 1 x 10(-4) M sanguinarine. The I50 for enzyme inhibition and the ED50 for the inotropic action of sanguinarine were the same (6-6.5 x 10(-6) M) indicating that both effects may be causally related.

MeSH terms

  • Alkaloids / pharmacology*
  • Animals
  • Benzophenanthridines
  • Cardiotonic Agents / pharmacology*
  • Guinea Pigs
  • In Vitro Techniques
  • Isoquinolines
  • Myocardial Contraction / drug effects
  • Myocardium / enzymology*
  • Ouabain / pharmacology
  • Phenanthridines / pharmacology*
  • Sodium-Potassium-Exchanging ATPase / antagonists & inhibitors*

Substances

  • Alkaloids
  • Benzophenanthridines
  • Cardiotonic Agents
  • Isoquinolines
  • Phenanthridines
  • Ouabain
  • sanguinarine
  • Sodium-Potassium-Exchanging ATPase