Tumor necrosis factor-alpha downregulates the voltage gated outward K+ current in cultured neonatal rat cardiomyocytes: a possible cause of electrical remodeling in diseased hearts

Circ J. 2006 May;70(5):605-9. doi: 10.1253/circj.70.605.

Abstract

Background: Inflammatory cytokines have been reported to contribute to the progression of cardiac remodeling in various heart diseases and a remarkable prolongation of the monophasic action potential duration and reductions in the expression of Kv4.2 and K+ channel-interacting protein-2 (KChIP-2) in a rat autoimmune myocarditis model have been documented. In this study, the effect of tumor necrosis factor-alpha (TNF-alpha) on cultured cardiomyocytes was evaluated, focusing on the change in the voltage-gated outward K+ current and expression of related molecules.

Methods and results: Cardiomyocytes isolated from 1-day-old Lewis rats were cultured for 72 h and treated with TNF-alpha (50 ng/ml) for an additional 48 h. The myocytes treated with TNF-alpha showed a 22% reduction in the peak K+ current, which consisted of a transient outward K+ current (Ito) and 1.4-fold enhancement of the cell-capacitance in comparison with the control. Among the cardiac ion channel related molecules evaluated in this study, Kv4.2 and KChIP-2 mRNA exhibited remarkable reductions (p < 0.05).

Conclusions: Treatment with TNF-alpha induced reductions in Ito as well as cellular hypertrophy in neonatal cultured myocytes, which indicates that TNF-alpha might play a role in promoting electrical remodeling of cardiomyocytes under inflammatory conditions.

MeSH terms

  • Action Potentials
  • Animals
  • Animals, Newborn
  • Cells, Cultured
  • Disease Models, Animal
  • Down-Regulation / drug effects
  • Down-Regulation / genetics
  • Heart Diseases / pathology
  • Heart Diseases / physiopathology
  • Hypertrophy / chemically induced
  • Hypertrophy / pathology
  • Kv Channel-Interacting Proteins / drug effects*
  • Kv Channel-Interacting Proteins / genetics
  • Myocarditis / immunology
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism*
  • Myocytes, Cardiac / pathology
  • Potassium / metabolism*
  • Potassium Channels, Voltage-Gated / drug effects*
  • Potassium Channels, Voltage-Gated / genetics
  • RNA, Messenger / analysis
  • Rats
  • Rats, Inbred Lew
  • Shal Potassium Channels / drug effects*
  • Shal Potassium Channels / genetics
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Kcnip2 protein, rat
  • Kv Channel-Interacting Proteins
  • Potassium Channels, Voltage-Gated
  • RNA, Messenger
  • Shal Potassium Channels
  • TNF protein, human
  • Tumor Necrosis Factor-alpha
  • Potassium