Kinetic Model of Nav1.5 Channel Provides a Subtle Insight into Slow Inactivation Associated Excitability in Cardiac Cells

被引:6
作者
Zhang, Zheng [1 ]
Zhao, Zhiwen [1 ]
Liu, Yongfeng [1 ]
Wang, Wei [1 ]
Wu, Ying [1 ]
Ding, Jiuping [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Life Sci & Technol, Minist Educ, Key Lab Mol Biophys, Wuhan 430074, Hubei, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 05期
关键词
MUSCLE SODIUM-CHANNEL; SCN5A MUTATIONS; NA+ CHANNELS; VENTRICULAR MYOCYTES; GIANT-AXONS; CHANNELOPATHIES; SKELETAL; CURRENTS; ACTIVATION; EXPRESSION;
D O I
10.1371/journal.pone.0064286
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Voltage-gated sodium channel Nav1.5 has been linked to the cardiac cell excitability and a variety of arrhythmic syndromes including long QT, Brugada, and conduction abnormalities. Nav1.5 exhibits a slow inactivation, corresponding to a duration-dependent bi-exponential recovery, which is often associated with various arrhythmia syndromes. However, the gating mechanism of Nav1.5 and the physiological role of slow inactivation in cardiac cells remain elusive. Here a 12-state two-step inactivation Markov model was successfully developed to depict the gating kinetics of Nav1.5. This model can simulate the Nav1.5 channel in not only steady state processes, but also various transient processes. Compared with the simpler 8-state model, this 12-state model is well-behaved in simulating and explaining the processes of slow inactivation and slow recovery. This model provides a good framework for further studying the gating mechanism and physiological role of sodium channel in excitable cells.
引用
收藏
页数:8
相关论文
共 42 条
  • [1] Cardiac sodium channelopathies
    Amin, Ahmad S.
    Asghari-Roodsari, Alaleh
    Tan, Hanno L.
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2010, 460 (02): : 223 - 237
  • [2] Na channel inactivation from open and closed states
    Armstrong, Clay M.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (47) : 17991 - 17996
  • [3] INACTIVATION OF SODIUM CHANNEL .2. GATING CURRENT EXPERIMENTS
    ARMSTRONG, CM
    BEZANILLA, F
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1977, 70 (05) : 567 - 590
  • [4] Coupling interactions between voltage sensors of the sodium channel as revealed by site-specific measurements
    Chanda, B
    Asamoah, OK
    Bezanilla, F
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 2004, 123 (03) : 217 - 230
  • [5] Tracking voltage-dependent conformational changes in skeletal muscle sodium channel during activation
    Chanda, B
    Bezanilla, F
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 2002, 120 (05) : 629 - 645
  • [6] Theoretical investigation of the neuronal Na+ channel SCN1A:: abnormal gating and epilepsy
    Clancy, CE
    Kass, RS
    [J]. BIOPHYSICAL JOURNAL, 2004, 86 (04) : 2606 - 2614
  • [7] Impaired slow inactivation in mutant sodium channels
    Cummins, TR
    Sigworth, FJ
    [J]. BIOPHYSICAL JOURNAL, 1996, 71 (01) : 227 - 236
  • [8] IONIC CURRENTS CONTRIBUTING TO THE ACTION-POTENTIAL IN SINGLE VENTRICULAR MYOCYTES OF THE GUINEA-PIG STUDIED WITH ACTION-POTENTIAL CLAMP
    DOERR, T
    DENGER, R
    DOERR, A
    TRAUTWEIN, W
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1990, 416 (03): : 230 - 237
  • [9] GOLDMAN L, 1972, J GEN PHYSIOL, V59, P659, DOI 10.1085/jgp.59.6.659
  • [10] Human embryonic kidney (HEK293) cells express endogenous voltage-gated sodium currents and Nav1.7 sodium channels
    He, Bingjun
    Soderlund, David M.
    [J]. NEUROSCIENCE LETTERS, 2010, 469 (02) : 268 - 272