Cardiac Na+ current regulation by pyridine nucleotides

Circ Res. 2009 Oct 9;105(8):737-45. doi: 10.1161/CIRCRESAHA.109.197277. Epub 2009 Sep 10.

Abstract

Rationale: Mutations in glycerol-3-phosphate dehydrogenase 1-like (GPD1-L) protein reduce cardiac Na+ current (I(Na)) and cause Brugada Syndrome (BrS). GPD1-L has >80% amino acid homology with glycerol-3-phosphate dehydrogenase, which is involved in NAD-dependent energy metabolism.

Objective: Therefore, we tested whether NAD(H) could regulate human cardiac sodium channels (Na(v)1.5).

Methods and results: HEK293 cells stably expressing Na(v)1.5 and rat neonatal cardiomyocytes were used. The influence of NADH/NAD+ on arrhythmic risk was evaluated in wild-type or SCN5A(+/-) mouse heart. A280V GPD1-L caused a 2.48+/-0.17-fold increase in intracellular NADH level (P<0.001). NADH application or cotransfection with A280V GPD1-L resulted in decreased I(Na) (0.48+/-0.09 or 0.19+/-0.04 of control group, respectively; P<0.01), which was reversed by NAD+, chelerythrine, or superoxide dismutase. NAD+ antagonism of the Na+ channel downregulation by A280V GPD1-L or NADH was prevented by a protein kinase (PK)A inhibitor, PKAI(6-22). The effects of NADH and NAD+ were mimicked by a phorbol ester and forskolin, respectively. Increasing intracellular NADH was associated with an increased risk of ventricular tachycardia in wild-type mouse hearts. Extracellular application of NAD+ to SCN5A(+/-) mouse hearts ameliorated the risk of ventricular tachycardia.

Conclusions: Our results show that Na(v)1.5 is regulated by pyridine nucleotides, suggesting a link between metabolism and I(Na). This effect required protein kinase C activation and was mediated by oxidative stress. NAD+ could prevent this effect by activating PKA. Mutations of GPD1-L may downregulate Na(v)1.5 by altering the oxidized to reduced NAD(H) balance.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Benzophenanthridines / pharmacology
  • Brugada Syndrome / genetics
  • Brugada Syndrome / metabolism*
  • Cell Line
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Cyclic AMP-Dependent Protein Kinases / genetics
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Down-Regulation / drug effects
  • Down-Regulation / genetics
  • Enzyme Inhibitors / pharmacology
  • Glycerolphosphate Dehydrogenase / genetics
  • Glycerolphosphate Dehydrogenase / metabolism*
  • Humans
  • Mice
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Mutation*
  • Myocardium / metabolism
  • NAD / genetics
  • NAD / metabolism*
  • NAV1.5 Voltage-Gated Sodium Channel
  • Oxidation-Reduction
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / genetics
  • Protein Kinase C / metabolism
  • Rats
  • Sodium / metabolism*
  • Sodium Channels / genetics
  • Sodium Channels / metabolism*
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Tachycardia, Ventricular / genetics
  • Tachycardia, Ventricular / metabolism

Substances

  • Antineoplastic Agents
  • Benzophenanthridines
  • Enzyme Inhibitors
  • Muscle Proteins
  • NAV1.5 Voltage-Gated Sodium Channel
  • SCN5A protein, human
  • Scn5a protein, mouse
  • Scn5a protein, rat
  • Sodium Channels
  • NAD
  • Sodium
  • chelerythrine
  • GPD1L protein, human
  • Glycerolphosphate Dehydrogenase
  • Superoxide Dismutase
  • Cyclic AMP-Dependent Protein Kinases
  • Protein Kinase C