I(Kr) contributes to the altered ventricular repolarization that determines long-term cardiac memory

Cardiovasc Res. 2006 Jul 1;71(1):88-96. doi: 10.1016/j.cardiores.2006.02.028. Epub 2006 Mar 3.

Abstract

Objective: Cardiac memory (CM) is characterized by an altered T-wave morphology, which reflects altered repolarization gradients. We hypothesized that the delayed rectifier currents, I(Kr) and I(Ks), might contribute to these repolarization changes.

Methods: We studied conscious, chronically instrumented dogs paced from the postero-lateral left ventricular (LV) wall at rates 5-10% faster than sinus rate for 3 weeks. ECGs during sinus rhythm were recorded on days 0, 7, 14 and 21 of pacing. Within 3 weeks, CM achieved steady state, hearts were excised, and epicardial and endocardial tissues and myocytes were studied.

Results: In unpaced controls, action potential duration to 50% and 90% repolarization (APD) in epicardium was shorter than in endocardium (P < 0.05); in CM epicardial APD increased at CL > or = 500 ms, while endocardial APD was either unchanged or decreased such that the transmural gradient seen in controls diminished (P < 0.05). A transmural I(Kr) gradient occurred in controls (epicardium>endocardium, P < 0.05) and was reversed in CM. No I(Ks) transmural gradient was found in controls, while in CM endocardial I(Ks) was greater than epicardial at greater than +50 mV. Canine ERG (cERG) mRNA and protein in epicardium > endocardium in controls (P < 0.05), and this difference was lost in CM. Expression levels of KCNQ1 and KCNE1 protein were similar in all groups.

Conclusions: A transcriptionally induced change in epicardial I(Kr) contributes to the altered ventricular repolarization that characterizes CM.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Action Potentials / physiology*
  • Animals
  • Blotting, Western / methods
  • Cardiac Pacing, Artificial
  • Dogs
  • Electrocardiography
  • Endocardium / metabolism
  • Endocardium / physiology
  • Ether-A-Go-Go Potassium Channels / analysis
  • Ether-A-Go-Go Potassium Channels / genetics
  • Heart Ventricles
  • KCNQ1 Potassium Channel / analysis
  • KCNQ1 Potassium Channel / genetics
  • Membrane Potentials / physiology
  • Myocytes, Cardiac / metabolism*
  • Patch-Clamp Techniques
  • Pericardium / metabolism
  • Pericardium / physiology*
  • Potassium Channels, Inwardly Rectifying / physiology*
  • Potassium Channels, Voltage-Gated / analysis
  • Potassium Channels, Voltage-Gated / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Ventricular Remodeling

Substances

  • Ether-A-Go-Go Potassium Channels
  • KCNE1 protein, human
  • KCNQ1 Potassium Channel
  • KCNQ1 protein, human
  • Potassium Channels, Inwardly Rectifying
  • Potassium Channels, Voltage-Gated