Mechanisms underlying conduction slowing and arrhythmogenesis in nonischemic dilated cardiomyopathy

Fadi G. Akar, David D. Spragg, Richard S. Tunin, David A. Kass, Gordon F. Tomaselli

Research output: Contribution to journalArticle

242 Citations (Scopus)

Abstract

Heart Failure (HF) is associated with an increased risk of sudden death caused by ventricular tachyarrhythmias. Recent studies have implicated repolarization abnormalities and, in particular, exaggerated heterogeneity of transmural repolarization in the genesis of polymorphic ventricular tachycardia in a canine model of nonischemic dilated cardiomyopathy. The presence and degree to which conduction abnormalities play a role in arrhythmogenesis in this model are uncertain. HF was produced in dogs by rapid RV-pacing for 3 to 4 weeks. High-resolution optical action potentials were recorded from epicardial and endocardial surfaces of arterially perfused canine wedge preparations isolated from LV and RV of normal and failing dogs. Cellular and molecular determinants of conduction were investigated using patch-clamp recordings, Western blot analysis, and immunocytochemistry. HF was associated with marked prolongation (by 33%) of the QRS duration of the volume conducted electrocardiogram and significant (>20%) slowing of epicardial and endocardial conduction velocities (CV) in both LV and RV. Cx43 expression was reduced by >40% in epicardial and endocardial layers of the LV, but was unchanged in the RV of failing hearts. Despite greater epicardial than endocardial Cx43 expression, epicardial CV was consistently slower (P<0.01). Immunocytochemical analysis revealed predominant colocalization of Cx43 with N-cadherin in normal versus failing samples, because Cx43 was redistributed from the intercalated disk to lateral cell borders in failing tissue. Moreover, a significant (P<0.05) increase in hypophosphorylated Cx43 was detected in the LV and RV of failing hearts. Action potential upstroke velocities in isolated ventricular myocytes from normal and failing hearts were not different (P=0.8, not significant), and Masson trichrome staining revealed no significant change in fibrosis content in HF. Nonischemic dilated cardiomyopathy is associated with significant slowing of CV that was not directly related to reduced Cx43 expression. Changes in phosphorylation and localization of Cx43 may contribute to gap-junction dysfunction, CV slowing, and arrhythmias in HF.

Original languageEnglish (US)
Pages (from-to)717-725
Number of pages9
JournalCirculation Research
Volume95
Issue number7
DOIs
StatePublished - Oct 1 2004
Externally publishedYes

Fingerprint

Connexin 43
Dilated Cardiomyopathy
Heart Failure
Action Potentials
Canidae
Dogs
Gap Junctions
Cadherins
Ventricular Tachycardia
Sudden Death
Tachycardia
Muscle Cells
Cardiac Arrhythmias
Electrocardiography
Fibrosis
Western Blotting
Immunohistochemistry
Phosphorylation
Staining and Labeling

Keywords

  • Arrhythmias
  • Connexin
  • Gap junctions
  • Heart failure
  • Optical mapping

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Mechanisms underlying conduction slowing and arrhythmogenesis in nonischemic dilated cardiomyopathy. / Akar, Fadi G.; Spragg, David D.; Tunin, Richard S.; Kass, David A.; Tomaselli, Gordon F.

In: Circulation Research, Vol. 95, No. 7, 01.10.2004, p. 717-725.

Research output: Contribution to journalArticle

Akar, Fadi G. ; Spragg, David D. ; Tunin, Richard S. ; Kass, David A. ; Tomaselli, Gordon F. / Mechanisms underlying conduction slowing and arrhythmogenesis in nonischemic dilated cardiomyopathy. In: Circulation Research. 2004 ; Vol. 95, No. 7. pp. 717-725.
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