High sensitivity of the Na+, K+-pump of human red blood cells to genins of cardiac glycosides
Open Access
- 1 April 1988
- journal article
- research article
- Published by Wiley in British Journal of Pharmacology
- Vol. 93 (4) , 803-810
- https://doi.org/10.1111/j.1476-5381.1988.tb11465.x
Abstract
1 Four different cardiac glycosides (ouabain, digitoxin, digoxin and gitoxin) and their corresponding genins were tested on Na+, K+-pump fluxes measured under steady-state and initial rate conditions (non equilibrium conditions) in human and rat erythrocytes and in mouse macrophages. 2 In human red cells, Na+, K+-pump fluxes exhibited up to 8 fold higher sensitivity to genins than to glycosides. In addition genins, but not the corresponding glycosides, exhibited double reactivity with regard to the erythrocyte Na+, K+-pump (with the exception of gitoxigenin). A weak reactivity component was similar to the one of the corresponding glycosides (IC50 of about 10−6 m) and a high reactivity component exhibited IC50 values varying from 0.1 to 0.5 × 10−6 m for digitoxigenin and ouabagenin respectively. 3 In contrast with human red cells, the initial rate of Na+, K+-pump fluxes in rat erythrocytes and mouse macrophages was less sensitive to genins than to the corresponding cardiac glycosides. 4 Dihydroouabain was 3, 10 and 75 times less active than ouabain in inhibiting the initial rate of Na+, K+-pump fluxes in human and rat erythrocytes and in mouse macrophages respectively. 5 In conclusion, Na+, K+-pump fluxes measured under initial rate conditions in human erythrocytes exhibit an unusually high sensitivity to genins of cardiac glycosides. This property probably results from the fast binding rate constants of genins and the slow association rates of glycosides to human red cells.This publication has 26 references indexed in Scilit:
- Multiplicity of cardiac glycoside receptors in the heartTrends in Pharmacological Sciences, 1985
- The effect of cyclic AMP on Na+ and K+ transport systems in mouse macrophagesCellular and Molecular Life Sciences, 1985
- Influence of digitalis and diuretics on ouabain binding sites on human erythrocytesJournal of Molecular Medicine, 1984
- The inotropic effect of ouabain and its antagonism by dihydroouabain in rat isolated atria and ventricles in relation to specific binding sitesBritish Journal of Pharmacology, 1983
- Ca2+-free perfusion of rat heart reveals a (Na+ + K+) ATPase form highly sensitive to ouabainNature, 1982
- THE HUMAN ERYTHROCYTE Cl‐DEPENDENT Na‐K COTRANSPORT SYSTEM AS A POSSIBLE MODEL FOR STUDYING THE ACTION OF LOOP DIURETICSBritish Journal of Pharmacology, 1982
- Rubidium Uptake in ErythrocytesPublished by Springer Nature ,1981
- Inhibition of (Na+ + K+)-ATPase by ouabain: Involvement of calcium and membrane proteinsBiochimica et Biophysica Acta (BBA) - Biomembranes, 1979
- Cardenolide analogs. An explanation for the unusual properties of AY 22241European Journal of Pharmacology, 1979
- Reduction of the equilibrium binding of cardiac glycosides and related compounds to Na+, K+-ATPase as a possible mechanism for the potassium-induced reversal of their toxicityNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1978