Dissociation between ionic remodeling and ability to sustain atrial fibrillation during recovery from experimental congestive heart failure

Circulation. 2004 Jan 27;109(3):412-8. doi: 10.1161/01.CIR.0000109501.47603.0C. Epub 2004 Jan 12.

Abstract

Background: Congestive heart failure (CHF) downregulates atrial transient outward (I(to)), slow delayed rectifier (I(Ks)), and L-type Ca(2+) (I(Ca,L)) currents and upregulates Na(+)-Ca(2+) exchange current (I(NCX)) (ionic remodeling) and causes atrial fibrosis (structural remodeling). The relative importance of ionic versus structural remodeling in CHF-related atrial fibrillation (AF) is controversial.

Methods and results: We measured hemodynamic and echocardiographic parameters, mean duration of burst pacing-induced AF (DAF), and atrial-myocyte ionic currents in dogs with CHF induced by 2-week ventricular tachypacing (240 bpm), CHF dogs allowed to recover without pacing for 4 weeks (REC), and unpaced controls. Left ventricular ejection fraction averaged 58.6+/-1.2% (control), 36.2+/-2.3% (CHF, P<0.01), and 57.9+/-1.6% (REC), indicating full hemodynamic recovery. Similarly, left atrial pressures were 2.2+/-0.3 (control), 13.1+/-1.5 (CHF), and 2.4+/-0.4 (REC) mm Hg. CHF reduced I(to) density by approximately 65% (P<0.01), decreased I(Ca,L) density by approximately 50% (P<0.01), and diminished I(Ks) density by approximately 40% (P<0.01) while increasing I(NCX) density by approximately 110% (P<0.05). In REC, all ionic current densities returned to control values. DAF increased in CHF (1132+/-207 versus 14.3+/-8.8 seconds, control) and remained increased with REC (1014+/-252 seconds). Atrial fibrous tissue content also increased in CHF (2.1+/-0.2% for control versus 10.2+/-0.7% for CHF, P<0.01), with no recovery observed in REC (9.4+/-0.8%, P<0.01 versus control, P=NS versus CHF).

Conclusions: With reversal of CHF, there is complete recovery of ionic remodeling, but the prolonged-AF substrate and structural remodeling remain. This suggests that structural, not ionic, remodeling is the primary contributor to AF maintenance in experimental CHF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atrial Fibrillation / etiology*
  • Atrial Fibrillation / pathology
  • Atrial Fibrillation / physiopathology
  • Calcium Channels, L-Type / metabolism
  • Cells, Cultured
  • Delayed Rectifier Potassium Channels
  • Dogs
  • Electric Conductivity
  • Fibrosis
  • Heart Atria / pathology
  • Heart Failure / complications*
  • Hemodynamics
  • Ion Channels / metabolism*
  • Myocytes, Cardiac / physiology
  • Patch-Clamp Techniques
  • Potassium Channels / metabolism
  • Potassium Channels, Voltage-Gated*
  • Sodium-Calcium Exchanger / metabolism

Substances

  • Calcium Channels, L-Type
  • Delayed Rectifier Potassium Channels
  • Ion Channels
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Sodium-Calcium Exchanger