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
  • [21] Calcium-dependent Nedd4-2 upregulation mediates degradation of the cardiac sodium channel Nav1.5: implications for heart failure
    Luo, L.
    Ning, F.
    Du, Y.
    Song, B.
    Yang, D.
    Salvage, S. C.
    Wang, Y.
    Fraser, J. A.
    Zhang, S.
    Ma, A.
    Wang, T.
    ACTA PHYSIOLOGICA, 2017, 221 (01) : 44 - 58
  • [22] Lack of influence of sex hormones on Brugada syndrome-associated mutant Nav1.5 sodium channel
    Yang, Guodong
    Liu, Jing
    Wang, Ya
    Du, Yuan
    Ma, Aiqun
    Wang, Tingzhong
    JOURNAL OF ELECTROCARDIOLOGY, 2019, 52 : 82 - 87
  • [23] Interaction of the antiarrhythmic drug Amiodarone with the sodium channel Nav1.5 depends on the extracellular pH
    de Conceicao, Michael Ramon Lima
    Teixeira-Fonseca, Jorge Lucas
    Marques, Leisiane Pereira
    Souza, Diego Santos
    Roman-Campos, Danilo
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2023, 960
  • [24] The cardiac sodium channel gene SCN5A and its gene product Nav1.5: Role in physiology and pathophysiology
    Veerman, Christiaan C.
    Wilde, Arthur A. M.
    Lodder, Elisabeth M.
    GENE, 2015, 573 (02) : 177 - 187
  • [25] NaV1.5 sodium channel window currents contribute to spontaneous firing in olfactory sensory neurons
    Frenz, Christopher T.
    Hansen, Anne
    Dupuis, Nicholas D.
    Shultz, Nicole
    Levinson, Simon R.
    Finger, Thomas E.
    Dionne, Vincent E.
    JOURNAL OF NEUROPHYSIOLOGY, 2014, 112 (05) : 1091 - 1104
  • [26] Sodium Channel NaV1.5 Expression is Enhanced in Cultured Adult Rat Skeletal Muscle Fibers
    Morel, J.
    Rannou, F.
    Talarmin, H.
    Giroux-Metges, M. A.
    Pennec, J. P.
    Dorange, G.
    Gueret, G.
    JOURNAL OF MEMBRANE BIOLOGY, 2010, 235 (02) : 109 - 119
  • [27] The cardiac sodium current Nav1.5 is functionally expressed in rabbit bronchial smooth muscle cells
    Bradley, E.
    Webb, T. I.
    Hollywood, M. A.
    Sergeant, G. P.
    McHale, N. G.
    Thornbury, K. D.
    AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2013, 305 (04): : C427 - C435
  • [28] Sodium Channel NaV1.5 Expression is Enhanced in Cultured Adult Rat Skeletal Muscle Fibers
    J. Morel
    F. Rannou
    H. Talarmin
    M. A. Giroux-Metges
    J. P. Pennec
    G. Dorange
    G. Gueret
    Journal of Membrane Biology, 2010, 235 : 109 - 119
  • [29] Mechanistic insights into the interaction of cardiac sodium channel Nav1.5 with MOG1 and a new molecular mechanism for Brugada syndrome
    Xiong, Hongbo
    Bai, Xuemei
    Quan, Zhuang
    Yu, Dong
    Zhang, Hongfu
    Zhang, Chi
    Liang, Lina
    Yao, Yufeng
    Yang, Qin
    Wang, Zhijie
    Wang, Longfei
    Huang, Yuan
    Li, Hui
    Ren, Xiang
    Tu, Xin
    Ke, Tie
    Xu, Chengqi
    Wang, Qing K.
    HEART RHYTHM, 2022, 19 (03) : 478 - 489
  • [30] Ranolazine Decreases Mechanosensitivity of the Voltage-Gated Sodium Ion Channel NaV1.5 A Novel Mechanism of Drug Action
    Beyder, Arthur
    Strege, Peter R.
    Reyes, Santiago
    Bernard, Cheryl E.
    Terzic, Andre
    Makielski, Jonathan
    Ackerman, Michael J.
    Farrugia, Gianrico
    CIRCULATION, 2012, 125 (22) : 2698 - U95