Sequential dissection of multiple ionic currents in single cardiac myocytes under action potential-clamp

被引:53
作者
Banyasz, Tamas [2 ,3 ]
Horvath, Balazs
Jian, Zhong
Lzu, Leighton T.
Chen-Izu, Ye [1 ,4 ]
机构
[1] Univ Calif Davis, Dept Pharmacol, Dept Biomed Engn, Dept Med,Div Cardiol, Davis, CA 95616 USA
[2] Univ Debrecen, Dept Physiol, Debrecen, Hungary
[3] Hlth Sci Ctr, Debrecen, Hungary
[4] Univ Calif Davis, Dept Internal Med, Div Cardiol, Davis, CA 95616 USA
关键词
Action potential; AP-clamp; Cardiac; Arrhythmia; Ca2+ channel; K+ channel; VENTRICULAR MYOCYTES; CALCIUM CURRENT;
D O I
10.1016/j.yjmcc.2010.12.020
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The cardiac action potential (AP) is shaped by myriad ionic currents. In this study, we develop an innovative AP-clamp Sequential Dissection technique to enable the recording of multiple ionic currents in the single cell under AP-clamp. This new technique presents a significant step beyond the traditional way of recording only one current in any one cell. The ability to measure many currents in a single cell has revealed two hitherto unknown characteristics of the ionic currents in cardiac cells: coordination of currents within a cell and large variation of currents between cells. Hence, the AP-clamp Sequential Dissection method provides a unique and powerful tool for studying individual cell electrophysiology. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:578 / 581
页数:4
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