Altered Electrophysiological Properties of Coronary Artery in Isoprenaline-Induced Cardiac Hypertrophy

Altered Electrophysiological Properties of Coronary Artery in Isoprenaline-Induced Cardiac Hypertrophy

<P> An impaired smooth muscle cell (SMC) relaxation of coronary artery by alteration of K<SUP>&#8290;</SUP> channels would be the most potential explanation for reduced coronary reserve in left ventricular hypertrophy (LVH), however, this possibility has not been investigated. We performed morphometrical analysis of the coronary artery under electron microscopy and measured Ca<SUP>2&#8290;</SUP>-activated K (K<SUB>Ca</SUB>) currents and delayed rectifier K (K<SUB>dr</SUB>) currents by whole-cell and inside-out patch-clamp technique in single coronary arterial SMCs from rabbits subjected to isoprenaline-induced cardiac hypertrophy. Coronary arterial SMCs underwent significant changes in ultrastructure. The unitary current amplitude and the open-state probability of K<SUB>Ca</SUB> channel were significantly reduced in hypertrophy without open-time and closed-time kinetic. The concentration-response curve of K<SUB>Ca</SUB> channel to Ca<SUP>2&#8290;</SUP> is shifted to the right in hypertrophy. The reduction in the mean single channel current and increase in the open channel noise of K<SUB>Ca</SUB> channel by TEA were more sensitive in hypertrophy. K<SUB>dr</SUB> current density is significantly reduced in hypertrophy without activation and inactivation kinetics. The sensitivity of K<SUB>dr</SUB> current on 4-AP is significantly increased in hypertrophy. This is the first study to report evidence for alterations of K<SUB>Ca</SUB> channels and K<SUB>dr</SUB> channels in coronary SMCs with LVH. The findings may provide some insight into mechanism of the reduced coronary reserve in LVH.