Key Points
- To investigate the electrophysiological differences among epicardial, midmyocardial, and endocardial myocytes in canine ventricles.
- Used microelectrode and patch-clamp techniques to measure action potentials and currents in myocytes from canine left ventricle.
- Enzymatically dissociated myocytes were examined from epicardium, midmyocardial (M region), and endocardium.
- Assessed Ito1 and K+ currents among different myocyte layers.
- Epicardial and M region myocytes exhibited a prominent spike and dome in action potentials, while endocardial cells did not.
- Inward rectifier K+ current magnitudes were highest in epicardial cells (392 pA) compared to M region (289 pA) and endocardial (348 pA) cells.
- Ito1 amplitude was significantly greater in epicardial (4,203 pA) and M region (3,638 pA) compared to endocardial (714 pA) myocytes.
Structured PICO
PPopulationMyocytes enzymatically dissociated from discrete layers (epicardium, M region, and endocardium) of the free wall of the canine left ventricle
CComparatorComparison between epicardial, M region, and endocardial myocytes
OOutcomeTransmembrane action potentials, steady-state current-voltage relations, and the 4-aminopyridine-sensitive transient outward current (Ito1)surrogate
Prominent electrophysiological heterogeneity exists across the canine ventricular wall, driven importantly by differences in the transient outward current (Ito1), which may underlie ECG waveforms and arrhythmogenesis.