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分离的大鼠心肌细胞中快速钠电流的表征:钳制膜电位的模拟

Characterization of the fast sodium current in isolated rat myocardial cells: simulation of the clamped membrane potential.

作者信息

Bodewei R, Hering S, Lemke B, Rosenshtraukh L V, Undrovinas A I, Wollenberger A

出版信息

J Physiol. 1982 Apr;325:301-15. doi: 10.1113/jphysiol.1982.sp014151.

Abstract
  1. The fast sodium inward current of freshly isolated single rat myocardial cells was studied by means of the internal perfusion-voltage clamp method. 2. The voltage dependence of this current did not differ from the current-voltage characteristics of the fast sodium inward current described for other excitable cells and tissues. 3. The time constant of inactivation of the Na+ current of the isolated myocardial cells ranged between 5.2 msec at -58 mV and 0.5 msec at +18 mV. The activation time constant ranged from 0.3 msec at -55 mV to 70 microseconds at +10 mV. 4. The reactivation time constant of the maximum sodium current at a holding potential of -100 mV was found to be 21 +/- 5 msec. 5. A mathematical model was developed for the simulation and analysis of the influence of the series and shunt resistances on the time response of the membrane potential. The results of the modelling make it clear that control of the series and shunt resistances in any given experiment is a conditio sine qua non for a valid analysis of the kinetic parameters of the sodium inward current. 6. Sodium currents with delayed activation kinetics must be regarded as an indication of insufficient control of the membrane potential.
摘要
  1. 采用细胞内灌注-电压钳法研究了新鲜分离的单个大鼠心肌细胞的快速钠内向电流。2. 该电流的电压依赖性与其他可兴奋细胞和组织中描述的快速钠内向电流的电流-电压特性并无差异。3. 分离的心肌细胞钠电流的失活时间常数在-58 mV时为5.2毫秒,在+18 mV时为0.5毫秒。激活时间常数在-55 mV时为0.3毫秒,在+10 mV时为70微秒。4. 发现在-100 mV的钳制电位下,最大钠电流的再激活时间常数为21±5毫秒。5. 建立了一个数学模型,用于模拟和分析串联电阻和并联电阻对膜电位时间响应 的影响。建模结果表明,在任何给定实验中,控制串联电阻和并联电阻是有效分析钠内向电流动力学参数的必要条件。6. 具有延迟激活动力学的钠电流必须被视为膜电位控制不足的一个指标。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff24/1251395/9d719d9e7e0d/jphysiol00682-0311-a.jpg

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