Nitric oxide regulates cardiac intracellular Na⁺ and Ca²⁺ by modulating Na/K ATPase via PKCε and phospholemman-dependent mechanism

Research output: Contribution to journalArticle

Authors

  • Andrew R Hall
  • Erika J Kennington
  • Karen Aughton
  • Andrii Boguslavskyi
  • William Fuller
  • Sanda Despa
  • Donald M Bers
  • Michael J Shattock

Colleges, School and Institutes

Abstract

In the heart, Na/K-ATPase regulates intracellular Na(+) and Ca(2+) (via NCX), thereby preventing Na(+) and Ca(2+) overload and arrhythmias. Here, we test the hypothesis that nitric oxide (NO) regulates cardiac intracellular Na(+) and Ca(2+) and investigate mechanisms and physiological consequences involved. Effects of both exogenous NO (via NO-donors) and endogenously synthesized NO (via field-stimulation of ventricular myocytes) were assessed in this study. Field stimulation of rat ventricular myocytes significantly increased endogenous NO (18 ± 2 μM), PKCε activation (82 ± 12%), phospholemman phosphorylation (at Ser-63 and Ser-68) and Na/K-ATPase activity (measured by DAF-FM dye, western-blotting and biochemical assay, respectively; p<0.05, n=6) and all were abolished by Ca(2+)-chelation (EGTA 10mM) or NOS inhibition l-NAME (1mM). Exogenously added NO (spermine-NONO-ate) stimulated Na/K-ATPase (EC50=3.8 μM; n=6/grp), via decrease in Km, in PLM(WT) but not PLM(KO) or PLM(3SA) myocytes (where phospholemman cannot be phosphorylated) as measured by whole-cell perforated-patch clamp. Field-stimulation with l-NAME or PKC-inhibitor (2 μM Bis) resulted in elevated intracellular Na(+) (22 ± 1.5 and 24 ± 2 respectively, vs. 14 ± 0.6mM in controls) in SBFI-AM-loaded rat myocytes. Arrhythmia incidence was significantly increased in rat hearts paced in the presence of l-NAME (and this was reversed by l-arginine), as well as in PLM(3SA) mouse hearts but not PLM(WT) and PLM(KO). We provide physiological and biochemical evidence for a novel regulatory pathway whereby NO activates Na/K-ATPase via phospholemman phosphorylation and thereby limits Na(+) and Ca(2+) overload and arrhythmias. This article is part of a Special Issue entitled "Na(+) Regulation in Cardiac Myocytes".

Details

Original languageEnglish
Pages (from-to)164-171
Number of pages8
JournalJournal of Molecular and Cellular Cardiology
Volume61
Publication statusPublished - Aug 2013

Keywords

  • Action Potentials, Animals, Calcium, Calcium-Binding Proteins, Cytoplasm, Electric Stimulation, Heart Ventricles, In Vitro Techniques, Male, Membrane Proteins, Mice, Myocytes, Cardiac, NG-Nitroarginine Methyl Ester, Nitric Oxide, Nitric Oxide Synthase, Patch-Clamp Techniques, Phosphoproteins, Phosphorylation, Protein Kinase C-epsilon, Protein Processing, Post-Translational, Rats, Sodium, Sodium-Potassium-Exchanging ATPase