A comparison of transient outward currents in canine cardiac Purkinje cells and ventricular myocytes

被引:33
作者
Han, W
Wang, ZG
Nattel, S
机构
[1] Montreal Heart Inst, Res Ctr, Montreal, PQ H1T 1C8, Canada
[2] Montreal Heart Inst, Dept Med, Montreal, PQ H1T 1C8, Canada
[3] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
[4] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ H3G 1Y6, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2000年 / 279卷 / 02期
关键词
potassium channels; molecular biology of cardiac ion channels; cardiac arrhythmias; action potentials; potassium channel blockers; antiarrhythmic drugs;
D O I
10.1152/ajpheart.2000.279.2.H466
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although abnormalities in Purkinje cell (PC) repolarization are important causes of cardiac arrhythmias, the detailed properties of repolarizing currents in PCs are incompletely understood. We compared transient outward K+ current (I-to) in single PCs from canine false tendons with midmyocardial ventricular myocytes (VMs). I-to reactivation was biexponential, with a similar rapid-phase time constant (30 +/- 5 and 35 +/- 4 ms for VM and PC, respectively) but a large, slow component in PCs with a much greater time constant than VM (1,427 +/- 70 vs. 181 +/- 24 ms, P < 0.001). Tetraethylammonium had no effect on VM I-to but reversibly inhibited PC I-to (IC50 = 2.4 +/- 0.4 mM). PC I-to was also more sensitive to 4-aminopyridine (IC50 = 50 +/- 7 vs. 526 +/- 49 mu M in VM, P < 0.0001). H2O2 slowed I-to inactivation in PCs but did not affect VM I-to. We conclude that PC I-to shows significant differences from VM I-to, with some features, such as tetraethylammonium sensitivity, that have been reported in neither cardiac I-to of atrial or ventricular myocytes nor cloned K+ channel subunits (Kv1.4, Kv4.2, or Kv4.3) known to participate in cardiac I-to.
引用
收藏
页码:H466 / H474
页数:9
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