François Noël1, Pedro Azalim2, Fernando M do Monte2, Luis Eduardo M Quintas2, Adriana Katz3, Steven J D Karlish4. 1. Laboratório de Farmacologia Bioquímica e Molecular, ICB, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil. Electronic address: fnoel@pharma.ufrj.br. 2. Laboratório de Farmacologia Bioquímica e Molecular, ICB, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil. 3. Department of Biomolecular Sciences, Weizmann Institute of Science, Rehovoth, Israel. 4. Department of Biomolecular Sciences, Weizmann Institute of Science, Rehovoth, Israel. Electronic address: steven.karlish@weizmann.ac.il.
Abstract
INTRODUCTION: Ouabain and digoxin are classical inhibitors of the Na+,K+-ATPase. In addition to their conventional uses as therapeutic agents or experimental tools there is renewed interest due to evidence suggesting they could be endogenous hormones. Somewhat surprisingly, different publications show large discrepancies in potency for inhibiting Na+,K+-ATPase activity (IC50), particularly for the slow binding inhibitors, ouabain and digoxin. METHODS: Using purified pig kidney Na+,K+-ATPase (α1β1FXYD2) and purified detergent-soluble recombinant human Na+,K+-ATPase (α1β1FXYD1) we have re-evaluated binding and inhibition kinetics and effects of K+ concentration for ouabain, digoxin, ouabagenin and digoxigenin. RESULTS: We demonstrate unequivocally that for slow binding inhibitors, ouabain and digoxin, long incubation times (≥60 min at 37 °C) are required to avoid under-estimation of potency and correctly determine inhibition (IC50 around 100-200 nM at 5 mM K+) contrary to what occurs when pre-incubation of the drugs without ATP is followed by a short incubation time. By contrast, for the rapidly bound inhibitors, ouabagenin and digoxigenin, short incubation times suffice (<10 min). The strong reduction of inhibitory potency observed at high un-physiological K+ concentrations (≥5 mM) also explained the low potency reported by some authors. DISCUSSION: The data resolve discrepancies in the literature attributable to sub-optimal assay conditions. Similar IC50 values are obtained for pig kidney and recombinant human Na+,K+-ATPase, showing that inhibitory potencies are not determined by the species difference (pig versus human) or environment (membrane-bound versus detergent-soluble) of the Na+,K+-ATPase. The present methodological considerations are especially relevant for drug development of slow binding inhibitors.
INTRODUCTION:Ouabain and digoxin are classical inhibitors of the Na+,K+-ATPase. In addition to their conventional uses as therapeutic agents or experimental tools there is renewed interest due to evidence suggesting they could be endogenous hormones. Somewhat surprisingly, different publications show large discrepancies in potency for inhibiting Na+,K+-ATPase activity (IC50), particularly for the slow binding inhibitors, ouabain and digoxin. METHODS: Using purified pig kidney Na+,K+-ATPase (α1β1FXYD2) and purified detergent-soluble recombinant human Na+,K+-ATPase (α1β1FXYD1) we have re-evaluated binding and inhibition kinetics and effects of K+ concentration for ouabain, digoxin, ouabagenin and digoxigenin. RESULTS: We demonstrate unequivocally that for slow binding inhibitors, ouabain and digoxin, long incubation times (≥60 min at 37 °C) are required to avoid under-estimation of potency and correctly determine inhibition (IC50 around 100-200 nM at 5 mM K+) contrary to what occurs when pre-incubation of the drugs without ATP is followed by a short incubation time. By contrast, for the rapidly bound inhibitors, ouabagenin and digoxigenin, short incubation times suffice (<10 min). The strong reduction of inhibitory potency observed at high un-physiological K+ concentrations (≥5 mM) also explained the low potency reported by some authors. DISCUSSION: The data resolve discrepancies in the literature attributable to sub-optimal assay conditions. Similar IC50 values are obtained for pig kidney and recombinant human Na+,K+-ATPase, showing that inhibitory potencies are not determined by the species difference (pig versus human) or environment (membrane-bound versus detergent-soluble) of the Na+,K+-ATPase. The present methodological considerations are especially relevant for drug development of slow binding inhibitors.
Authors: Jéssica Martins de Moura Valadares; Sumit O Bajaj; Hongyan Li; Hua-Yu L Wang; Simone Cavalcante Silva; Israel José Pereira Garcia; Duane Gischewiski Pereira; Pedro Azalim; Luis Eduardo Menezes Quintas; François Noël; Vanessa Faria Cortes; George Augustine O'Doherty; Leandro Augusto Barbosa Journal: J Cell Biochem Date: 2021-09-22 Impact factor: 4.429