基础医学与临床 ›› 2013, Vol. 33 ›› Issue (12): 1523-1527.

• 研究论文 • 上一篇    下一篇

H2O2对新生大鼠心室肌细胞HCN通道电流的影响及其机制

郑明奇1,刘刚2,董梅2,吉立双1,于榛1   

  1. 1. 河北医科大学第一医院心内科
    2. 河北医科大学第一医院
  • 收稿日期:2013-03-13 修回日期:2013-04-28 出版日期:2013-12-05 发布日期:2013-11-28
  • 通讯作者: 刘刚 E-mail:cardio2004@163.com
  • 基金资助:
    自发性高血压大鼠心、脑、肾和肠系膜微动脉缝隙连接特性的比较研究》国家自然科学基金(国家自然科学基金);河北省自然科学基金;河北省医学科学研究重点课题计划;教育部留学回国人员科研启动基金

The Effects of H2O2 on the Hyperpolarization- Activated Cyclic Nucleotide-Gated Channel Current and its Mechanisms in Neonatal Rat Cardiomyocytes

  • Received:2013-03-13 Revised:2013-04-28 Online:2013-12-05 Published:2013-11-28
  • Contact: Gang Liu E-mail:cardio2004@163.com
  • Supported by:
    ;The Project Sponsored by the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry.

摘要: 目的 明确过氧化氢(H2O2)对新生大鼠心肌细胞超极化激活环核苷酸门控离子通道(HCN)电流的影响及其机制。方法 用胶原蛋白酶技术分离新生SD大鼠心室肌获得单一的心室肌细胞,用全细胞膜片钳技术记录HCN通道电流(If);提取心肌细胞膜蛋白,用Western blot检测HCN蛋白的表达。结果 1)将心室肌细胞暴露于H2O2(100?mol/L) 20min后,If显著增大(P<0.05);2)H2O2增大If电流可被酪氨酸蛋白激酶抑制剂Genistein或PP2显著抑制;增大的通道酪氨酸磷酸化水平也被减小(P<0.05);3)用硫氧还原蛋白受体阻断剂显著抑制H2O2增大的If(P<0.05);4)If也可被非特异性蛋白酪氨酸磷酸酶(PTPs)抑制剂显著增大(P<0.05)。结论 H2O2增大If,是通过ROS依赖性的酪氨酸蛋白激酶及其相关的硫氧还原蛋白系统,调控HCN通道的活性和表达。

关键词: 过氧化氢, HCN通道电流, c-Sr, 硫氧还原蛋白

Abstract: Objective To identify the effects of exogenous hydrogen peroxide on the Hyperpolarization-Activated Cyclic Nucleotide-Gated Channel (HCN) current and its mechanisms in Neonatal Rat Ventricle Cardiomyocytes (NRVM). Methods NRVM from 1- to 3-day-old Wister rats were prepared by collagenase digestion, and incubatd in 37℃, 95%CO2 for patch-clamp recording and western-blotting analysis. Results Our data shown that exposure (~20 min) of NRVM to H2O2 (100 μmol/L) markedly increased If density (4.7±0.6 pA/pF vs. 11.7±1.1 pA/pF) along increased conductance (Gmax: 48.7±5.6 pS/pF vs. 192.6±64.1 pS/pF), a shift in activation voltage (V1/2) to positive potentials (-81.2±1.6 mV vs. -64.7±2.0 mV) and increase rate of activation (tact) (523.4±24.7 ms vs. 337.5±24.9 ms). Moreover, stimulation by H2O2 was largely inhibited by the non-specific tyrosine kinase blocker genistein (1μmol/L) or the c-Src-specific inhibitor PP2 (10 μmol/L). Augmented tyrosine phosphorylation of HCN2 channels with H2O2 treatment by determined by H2O2 Western blot using the phosphotyrosine specific antibody 4G10. Furthermore, the augmented If current was inhibited by pre-treatment with Trx receptor inhibitor (Auranofin 10nmol/L; 13-cis-retinoic acid 1 μmol/L). On the other hand, If current of NRVMs was also increased by treated with non-specific PTP inhibitors, phenylarsine oxide (PAO 1 μmol/L) or Na-orthovanadate (Na3VO4 10 μmol/L). Conclusion These data suggest that the c-Src family of tyrosine kinase mediate the augmentation of If density by oxidant agent H2O2 via a redox mechanism involving the Trx system.

Key words: H2O2, HCN channel current, c-Src, Thioredoxin

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