Modulation of Na+/K+ pump in intact erythrocytes by cardioglycosides, steroid hormones and ouabain-like compounds

Gen Pharmacol. 1992 Jul;23(4):683-7. doi: 10.1016/0306-3623(92)90148-d.

Abstract

1. Pure erythrocytes preparations, free from platelets and white cells, were incubated for a long time without hemolysis. 2. Dose-response experiments performed with (a) cardioglycosides (ouabain and K-strophantoside), (b) steroid hormones and their glucuronides (tetrahydrocortisol, oestradiol and the respective 3-glucuronic derivatives) and (c) ouabain-like compounds purified in our laboratory (0.7 kDa and 2-4 kDa respectively) emphasise a modulatory effect [activation of Na+ efflux rate and K+ uptake at very low ligand concentrations, inhibition at higher levels; maximum enhancement of cation transport: (a) and (b) 10-0.1 nM (+40-50%), (c) 1-0.01 nM (2.5-fold)]. 3. Binding experiments show upward-curved Scatchard graphs, with the Kd values of 50 nM and 18 microM and the Bmax values of 10.2 and 984.5 fmol/100 microliters RBC (red blood cells) respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cardiac Glycosides / pharmacology*
  • Erythrocytes / drug effects
  • Erythrocytes / metabolism*
  • Female
  • Humans
  • Kinetics
  • Male
  • Ouabain / pharmacology*
  • Potassium / blood
  • Sodium / blood
  • Sodium-Potassium-Exchanging ATPase / physiology*
  • Steroids / pharmacology*

Substances

  • Cardiac Glycosides
  • Steroids
  • Ouabain
  • Sodium
  • Sodium-Potassium-Exchanging ATPase
  • Potassium