Shorofsky S R, January C T
Department of Medicine (Cardiology), University of Chicago, IL 60637.
Circ Res. 1992 Mar;70(3):456-64. doi: 10.1161/01.res.70.3.456.
Canine cardiac Purkinje cells contain both L- and T-type calcium currents, yet the single Ca2+ channels have not been characterized from these cells. Additionally, previous studies have shown an overlap between the steady-state inactivation and activations curves for L-type Ca2+ currents, suggesting the presence of L-type Ca2+ "window" current. We used the on-cell, patch-clamp technique to study Ca2+ channels from isolated cardiac Purkinje cells. Patches contained one or more Ca2+ channels 75% of the time. L-type channels were seen in 69% and T-type channels in 73% of these patches. With 110 mM Ba2+ as the charge carrier, the conductances of the L- and T-type Ca2+ channels were 24.2 +/- 0.8 pS (n = 9) and 9.0 +/- 0.5 pS (n = 8), respectively (mean +/- SEM). With 110 mM Ca2+ as the charge carrier, the conductance of the L-type Ca2+ channel decreased to 9.7 +/- 1.2 pS (n = 4), whereas the T-type Ca2+ channel conductance was unchanged. Voltage-dependent inactivation was shown for both L- and T-type Ca2+ channels, although for L-type Ca2+ channel with Ba2+ as the charge carrier, inactivation took at least 30 seconds at a potential of +40 mV. After channel inactivation was complete, L-type Ca2+ channel reopenings were observed following repolarizing steps into the window voltage range. Thus, our data identify both L- and T-type Ca2+ channels in cardiac Purkinje cells and demonstrate, at the single-channel level, L-type channel transitions expected for a window current. Window current may play an important role in shaping the action potential and in arrhythmogenesis.
犬心脏浦肯野细胞同时含有L型和T型钙电流,但尚未对这些细胞中的单个Ca2+通道进行特性描述。此外,先前的研究表明,L型Ca2+电流的稳态失活曲线和激活曲线存在重叠,提示存在L型Ca2+“窗电流”。我们采用细胞膜片钳技术研究分离的心脏浦肯野细胞中的Ca2+通道。75%的膜片中含有一个或多个Ca2+通道。在这些膜片中,69%可见L型通道,73%可见T型通道。以110 mM Ba2+作为载流子,L型和T型Ca2+通道的电导分别为24.2±0.8 pS(n = 9)和9.0±0.5 pS(n = 8)(平均值±标准误)。以110 mM Ca2+作为载流子,L型Ca2+通道的电导降至9.7±1.2 pS(n = 4),而T型Ca2+通道的电导未发生变化。L型和T型Ca2+通道均表现出电压依赖性失活,尽管对于以Ba2+作为载流子的L型Ca2+通道,在+40 mV电位下失活至少需要30秒。通道失活完成后,在复极化至窗电压范围内时可观察到L型Ca2+通道重新开放。因此,我们的数据鉴定了心脏浦肯野细胞中的L型和T型Ca2+通道,并在单通道水平上证明了窗电流预期的L型通道转变。窗电流可能在动作电位的形成和心律失常的发生中起重要作用。