Role of individual ionic current systems in ventricular cells hypothesized by a model study

被引:132
作者
Matsuoka, S
Sarai, N
Kuratomi, S
Ono, K
Noma, A [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Physiol & Biophys, Sakyo Ku, Kyoto 6068501, Japan
[2] Akita Univ, Sch Med, Dept Pharmacol, Akita 0108543, Japan
关键词
cardiac ventricular cell model; excitation contraction coupling; ion channel model; ion exchanger model;
D O I
10.2170/jjphysiol.53.105
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Individual ion channels or exchangers are described with a common set of equetions for both the sinoatrial node pacemaker and ventricular cells. New experimental data are included, such as the new kinetics of the inward rectifier K+ channel, delayed rectifier K+ channel, and sustained inward current. The gating model of Shirokov et al. (J Gen Physiol 102: 1005-1030, 1993) is used for both the fast Na+ and L-type Ca2+ channels. When combined with a contraction model (Negroni and Lascano: J Mol Cell Cardiol 28: 915'929, 1996), the experimental staircase phenomenon of contraction is reconstructed. The modulation of the action potential by varying the external Ca2+ and K+ concentrations is well simulated. The conductance of l(CaL) dominates membrane conductance during the action potential so that an artificial increase of l(to), l(Kr), l(Ks), or l(KATP) magnifies l(CaL) amplitude. Repolarizing current is provided sequentially by l(Ks), l(Kr), and l(K1). Depression of ATP production results in the shortening of action potential through the activation of l(KATP). The ratio of Ca2+ released from SR over Ca2+ entering via l(CaL) (Ca2+ gain=similar to15) in excitation-contraction coupling well agrees with the experimental data. The model serves as a predictive tool in generating testable hypotheses.
引用
收藏
页码:105 / 123
页数:19
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