Abstract
G.-R. L i, C.-P. L au and A. S hrier. Heterogeneity of Sodium Current in Atrial vs Epicardial Ventricular Myocytes of Adult Guinea Pig Hearts. Journal of Molecular and Cellular Cardiology (2002) 34, 1185–1194. The different sodium channel currents (INa) were reported in myocardium, neuron, and skeletal muscles. To study whether INa is homogeneous within the heart, we applied whole-cell voltage clamp technique to evaluate fast voltage-gated INa in atrial and ventricular myocytes isolated from guinea pig heart. It was found that the density of inward INa was 50% greater at −35mV in atrial (−42.6±2.9 pA/pF) than in ventricular (−27.5±1.8 pA/pF, P<0.01) myocytes. The half activation and inactivation voltages (V0.5) of INa in atrial myocytes were shifted 4.5±0.2 and 9.6±0.3mV negative to those of ventricular myocytes. Time constants forINa activation (τm) and inactivation (τh) were twice as rapid in atrial as in ventricular myocytes. The τm and τh were 0.34±0.03 and 1.36±0.07ms for atrial myocytes, and 0.69±0.05 and 3.27±0.23ms for ventricular myocytes, respectively. Recovery ofINa from inactivation was slower in atrial than in ventricular myocytes, whereas the development of resting state inactivation was more rapid in atrial (τ=67.5±4.3ms) than in ventricular (152.8±7.5ms, P<0.01) myocytes. The results reveal marked heterogeneity of INa in the density and biophysical properties in atrial and ventricular myocytes, and the study suggests the potential possibility of tissue specific cardiac sodium channel isoforms.
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