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咪唑安定对交感神经元全细胞钠通道电流的抑制作用
引用本文:郑吉健,庄心良,刘宝刚,杜冬萍,徐国辉.咪唑安定对交感神经元全细胞钠通道电流的抑制作用[J].金属学报,2000,5(2):108-111.
作者姓名:郑吉健  庄心良  刘宝刚  杜冬萍  徐国辉
作者单位:上海市第一人民医院麻醉科, 上海 200080
摘    要:目的 研究咪唑安定对交感神经元全细胞钠通道电流的影响,探讨其循环抑制机制。方法 酶消化法急性分离SD大鼠(8~12d)颈上交感神经节细胞,全细胞膜片钳技术记录咪唑安定对钠通道电流的影响。结果 在钳制电压-80mV,刺激电压0mV条件下,临床相关浓度的咪唑安定(0.3μmol·L-1)使钠通道电流峰值降低19.98%(P<0.05),随浓度增加,抑制作用逐渐增强,50%的钠通道电流峰值受抑制时的咪唑安定浓度(IC50)约为18.35μmol·L-1;3μmol·L-1的咪唑安定使钠电流稳态失活曲线产生明显的超极化方向移动(7.75mV,P<0.05),用药前、后50%的通道灭活时的条件脉冲电压(V1/2)分别为:-40.39mV、-48.14mV;3μmol·L-1的咪唑安定对钠电流的激活曲线几乎无影响。结论 临床相关浓度的咪唑安定对交感神经节全细胞钠通道电流有明显的抑制作用,且主要与钠通道的失活有关。提示咪唑安定的循环抑制作用可能与其直接抑制交感神经有关。

关 键 词:咪唑安定  交感神经节  钠通道  膜片钳  
收稿时间:2000-03-06
修稿时间:2000-04-10

Inhibition of midazolam on macroscopic sodium currents in ratsympathetic neurons
ZHENG Ji-Jian,ZHUANG Xin-Liang,LIU Bao-Gang,DU Dong-Ping,XU Guo-Hui.Inhibition of midazolam on macroscopic sodium currents in ratsympathetic neurons[J].Acta Metallurgica Sinica,2000,5(2):108-111.
Authors:ZHENG Ji-Jian  ZHUANG Xin-Liang  LIU Bao-Gang  DU Dong-Ping  XU Guo-Hui
Affiliation:Department of Anesthesiology, S hanghai First People's Hospital, Shanghai Medical University, Shanghai, 200080
Abstract:Aim The effects of midazolam on the whole-cell sodium currents in ratsympathetic neurons werestudied to explorethe mechanisms whereby midazolam mediates hypotension.Methods Whole-cell patch-clamprecordings wereperformed on enzymatically isolated ratsuperior cervical sympathetic neurons.Results Midazolam do se-dependent ly blocked the whole-cell sodiumcurrents evoked by a voltagestep to 0 mV from a holding potential of-80 mV with a mean drug concentration required toproduce 50 % currentinhibition (IC50)values of 18.35 μmol·L-1; Clinically relevant concentration of midazolam(0.3 μmol·L-1)reduced sodium peak cur rents by 19.98%(P<0.05);3 μmol·L-1 midazolam didn't affect the shape of I-V curves of sodium cur rents, butreduced the peak values by 21.75%.Similarly, 3 μmol·L-1 midazolam didn't cause significantshif tin the voltage-dependence of activation curve either.However, 3 μmol·L-1 midazolam caused a substantial hyperpolari zingshif t of the steady-state inactivation curve (7.75 mV, P<0.05), thatis the conditioning pulse potential at whih half-max imal channel is inactiva ted (V 1/2)was changed from-40.39 mV to-48.14 mV.Conclusion Clinically relevant concentration of midazolam has significantinhibition on sympathetic neurons.This inhibition is dose-dependent and relavant to the inactivation of sodium channel.The circulation depression of midazolam may berelevant to the di rectsuppresion of sympathetic neurons.
Keywords:midazolam  sympathetic ganglion  sodium channel  patch-clamp  
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