Acute and chronic effects of taurine magnesium coordination compound on cardiac sodium channel Nav1.5

被引:0
|
作者
Zhao, Lin [1 ]
Yang, Xiao-Xu [2 ]
Yin, Yong-Qiang [3 ]
Wu, Hong [3 ,4 ]
Kang, Yi [3 ]
Lou, Jian-Shi [3 ]
机构
[1] Tianjin Med Univ, Int Med Sch, Tianjin 300070, Peoples R China
[2] Tianjin Med Univ, Dept Pharm, Metab Dis Hosp, Tianjin 300070, Peoples R China
[3] Tianjin Med Univ, Dept Pharmacol, 22 Qixiangtai Rd, Tianjin 300070, Peoples R China
[4] Mudanjiang Med Univ, Dept Pharmacol, Mudanjiang 157011, Heilongjiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Nav1.5; sodium current; taurine magnesium; coordination compound; arrhythmia; IC50; HEK cells; whole-cell patch clamp technique; ANTIARRHYTHMIC-DRUGS; CLASS-I; ARRHYTHMIAS; REPOLARIZATION; DYSFUNCTION; EXPRESSION; MUTATIONS;
D O I
10.3892/mmr.2017.7117
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It has been previously demonstrated that taurine magnesium coordination compound (TMCC) produces antiarrhythmic effects in vivo. The present study investigated the acute and chronic effect of TMCC on sodium channels in HEK cells stably expressing human cardiac Nav1.5 sodium channels. The current amplitude, activation and inactivation kinetics, recovery time from inactivation, and use-dependent block of sodium channels were analyzed using the whole-cell patch clamp technique. Western blotting was used to analyze Nav1.5 expression following chronic TMCC treatment. In HEK cells expressing Nav1.5 channels, TMCC acutely inhibited Na+ currents in a dose-dependent manner. In addition, acute application of TMCC shifted the activation and inactivation curves, and prolonged the recovery time from inactivation, but did not exhibit a use-dependent block of Nav1.5. By contrast, chronic TMCC treatment only produced a use-dependent block of Nav1.5 and downregulated Nav1.5 expression. The results of the present study suggested that TMCC may produce antiarrhythmic actions via acute inhibition of sodium channel currents and chronic downregulation of Nav1.5 expression.
引用
收藏
页码:4259 / 4264
页数:6
相关论文
共 50 条
  • [1] Cardiac Sodium Channel Nav1.5 Mechanosensitivity Is Inhibited by Ranolazine
    Abriel, Hugues
    CIRCULATION, 2012, 125 (22) : 2681 - 2683
  • [2] SUMOylation of the cardiac sodium channel NaV1.5 modifies inward current and cardiac excitability
    Yoon, Jin-Young
    Greiner, Alexander M.
    Jacobs, Julia S.
    Kim, Young-Rae
    Rasmussen, Tyler P.
    Kutschke, William J.
    Matasic, Daniel S.
    Vikram, Ajit
    Gaddam, Ravinder R.
    Mehdi, Haider
    Irani, Kaikobad
    London, Barry
    HEART RHYTHM, 2023, 20 (11) : 1548 - 1557
  • [3] Modulation of the cardiac sodium channel NaV1.5 peak and late currents by NAD+ precursors
    Matasic, Daniel S.
    Yoon, Jin-Young
    McLendon, Jared M.
    Mehdi, Haider
    Schmidt, Mark S.
    Greiner, Alexander M.
    Quinones, Pravda
    Morgan, Gina M.
    Boudreau, Ryan L.
    Irani, Kaikobad
    Brenner, Charles
    London, Barry
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2020, 141 : 70 - 81
  • [4] Acute Reduction Of Cardiac Sodium Channel Nav1.5 Increases Mitochondrial Calcium And Rewires Cardiac Metabolism
    Zhang, Xiaoming
    McLendon, Jared
    Anderson, Ethan J.
    London, Barry
    Boudreau, Ryan L.
    CIRCULATION RESEARCH, 2022, 131
  • [5] UBC9 regulates cardiac sodium channel Nav1.5 ubiquitination, degradation and sodium current density
    Tang, Bo
    Hu, Yushuang
    Wang, Zhijie
    Cheng, Chen
    Wang, Pengyun
    Liang, Lina
    Xiong, Hongbo
    Luo, Chunyan
    Xu, Chengqi
    Chen, Qiuyun
    Wang, Qing Kenneth
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2019, 129 : 79 - 91
  • [6] Targeting the Sodium Channel NaV1.5 to Specific Membrane Compartments of Cardiac Cells Not a Simple Task!
    Shy, Diana
    Gillet, Ludovic
    Abriel, Hugues
    CIRCULATION RESEARCH, 2014, 115 (11) : 901 - 903
  • [7] Provocation of an Autoimmune Response to Cardiac Voltage-Gated Sodium Channel NaV1.5 Induces Cardiac Conduction Defects in Rats
    Korkmaz, Sevil
    Zitron, Edgar
    Bangert, Anna
    Seyler, Claudia
    Li, Shiliang
    Hegedues, Peter
    Scherer, Daniel
    Li, Jin
    Fink, Thomas
    Schweizer, Patrick A.
    Giannitsis, Evangelos
    Karck, Matthias
    Szabo, Gabor
    Katus, Hugo A.
    Kaya, Ziya
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2013, 62 (04) : 340 - 349
  • [8] Regulation of the cardiac sodium channel Nav1.5 by utrophin in dystrophin-deficient mice
    Albesa, Maxime
    Ogrodnik, Jakob
    Rougier, Jean-Sebastien
    Abriel, Hugues
    CARDIOVASCULAR RESEARCH, 2011, 89 (02) : 320 - 328
  • [9] Calmodulin binds to the N-terminal domain of the cardiac sodium channel Nav1.5
    Wang, Zizun
    Vermij, Sarah H.
    Sottas, Valentin
    Shestak, Anna
    Ross-Kaschitza, Daniela
    Zaklyazminskaya, Elena, V
    Hudmon, Andy
    Pitt, Geoffrey S.
    Rougier, Jean-Sebastien
    Abriel, Hugues
    CHANNELS, 2020, 14 (01) : 268 - 286
  • [10] Popeye domain containing proteins modulate the voltage-gated cardiac sodium channel Nav1.5
    Rinne, Susanne
    Kiper, Aytug K.
    Jacob, Ralf
    Ortiz-Bonnin, Beatriz
    Schindler, Roland F. R.
    Fischer, Sabine
    Komadowski, Marlene
    De Martino, Emilia
    Schaefer, Martin K. -H.
    Cornelius, Tamina
    Fabritz, Larissa
    Helker, Christian S. M.
    Brand, Thomas
    Decher, Niels
    ISCIENCE, 2024, 27 (05)