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The effect of protein kinase C on voltage-gated potassium channel in pulmonary artery smooth muscle cells from rats exposed to chronic hypoxia

机译:蛋白激酶C对慢性缺氧大鼠肺动脉平滑肌细胞电压门控钾通道的影响

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摘要

Background Chronic hypoxia can cause pulmonary hypertension and pulmonary heart disease with high mortality.The signal transduction pathway of protein kinase C (PKC) plays an important role in chronic pulmonary hypertension. So it is necessary to investigate the effect of PKC on voltage-gated potassium (K+) channels in pulmonary artery smooth muscle cells of rats exposed to chronic hypoxia.Methods Male Wistar rats were randomly divided into a control group (group A) and a chronic hypoxia group (group B). Group B received hypoxia [oxygen concentration (10±1)%] eight hours per day for four consecutive weeks. Single pulmonary artery smooth muscle cells were obtained using an acute enzyme separation method. Conventional whole cell patch clamp technique was used to record resting membrane potential, membrane capacitance and voltage-gated K+ currents. The changes in voltage-gated K+ currents before and after applying paramethoxyamphetamine (PMA) (500 nmol/L), an agonist of PKC, and PMA plus carbohydrate mixture of glucose, fructose and xylitol (GFX) (30 nmol/L), an inhibitor of PKC, were compared between the two groups. Results The resting membrane potential in group B was significantly lower than that of group A: -(29.0±4.8) mV (n=18) vs -(42.5±4.6) mV (n=35) (P<0.01). But there was no change in membrane capacitance between the two groups: (17.9±4.6) pF (n=40) vs (19.7±5.8) pF (n=31) (P>0.05). The voltage-gated K+ currents were significantly inhibited by PMA in group A, and this effect was reversed by GFX. However, the voltage-gated K+ currents in group B were not affected by PMA.Conclusions The resting membrane potential and voltage-gated K+ currents in pulmonary artery smooth muscle cells from rats exposed to chronic hypoxia decreased significantly. It seems that PKC has different effects on the voltage-gated K+ currents of pulmonary artery smooth muscle cells under different conditions.
机译:背景慢性低氧可引起肺动脉高压和肺源性心脏病,死亡率高。蛋白激酶C(PKC)的信号转导通路在慢性肺动脉高压中起重要作用。因此有必要研究PKC对慢性缺氧大鼠肺动脉平滑肌细胞电压门控钾(K +)通道的影响。方法将雄性Wistar大鼠随机分为对照组(A组)和慢性组(C组)。缺氧组(B组)。 B组连续八周每天缺氧[氧气浓度(10±1)%]。使用急性酶分离法获得单个肺动脉平滑肌细胞。使用常规的全细胞膜片钳技术记录静息膜电位,膜电容和电压门控K +电流。在应用对甲氧基苯丙胺(PMA)(500 nmol / L),PKC和PMA的激动剂以及葡萄糖,果糖和木糖醇(GFX)的碳水化合物混合物(30 nmol / L)之前和之后,电压门控K +电流的变化比较两组间PKC的抑制剂。结果B组静息膜电位明显低于A组:-( 29.0±4.8)mV(n = 18)vs-(42.5±4.6)mV(n = 35)(P <0.01)。但是两组之间的膜电容没有变化:(17.9±4.6)pF(n = 40)vs(19.7±5.8)pF(n = 31)(P> 0.05)。 A组中的PMA显着抑制了电压门控的K +电流,GFX逆转了这种效应。然而,B组的电压门控性K +电流不受PMA的影响。结论慢性缺氧大鼠肺动脉平滑肌细胞的静息膜电位和电压门控性K +电流明显降低。在不同条件下,PKC似乎对肺动脉平滑肌细胞的电压门控K +电流有不同的影响。

著录项

  • 来源
    《中华医学杂志(英文版)》 |2004年第1期|19-23|共5页
  • 作者单位

    Department of Respiratory Disease, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan 430030, China;

    Department of Respiratory Disease, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan 430030, China;

    Department of Respiratory Disease, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan 430030, China;

    Department of Respiratory Disease, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan 430030, China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 基础医学;
  • 关键词

    pulmonary artery; protein kinase C; hypoxia; ion channel;

    机译:肺动脉;蛋白激酶C;缺氧;离子通道;
  • 入库时间 2022-08-19 04:00:44
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