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鸡胚心脏细胞阈下起搏电流分析

Analysis of subthreshold pace-maker currents in chick embryonic heart cells.

作者信息

Clay J R, Shrier A

出版信息

J Physiol. 1981 Mar;312:471-90. doi: 10.1113/jphysiol.1981.sp013639.

Abstract
  1. Small re-aggregates of cells dissociated from the ventricles of 7-day-old chick embryonic hearts beat spontaneously in low external potassium concentration (Ko = 1.3 mM) tissue culture medium. This activity was blocked by the addition of tetrodotoxin (TTX) or potassium ions to the external medium. 2. A two-micro-electrode voltage-clamp technique was used to analyse the subthreshold currents responsible for the pace-maker depolarization. 3. Voltage-clamp steps 6-10 sec in duration revealed a time-dependent current having first order kinetics. Its membrane potential range of steady-state activation was -90 to -60 mV. 4. The current kinetics were qualitatively similar to those of Hodgkin & Huxley (1952b) with a peak time constant of approximately 1 sec at V = -75 mV. The kinetics were independent of Ko. 5. The time-dependent current was attributed to gated membrane channels. The fully activated current-voltage (I-V) relation of the channels was determined from the ratio of the amplitudes of the time-dependent currents during and after voltage-clamp steps following the procedure of Noble & Tsien (1968). 6. The fully activated I-V relation displayed inward rectification with negative slope conductance at potentials more than 15 mV positive to its reversal potential. Changes of Ko shifted the I-V curve along the voltage axis like a potassium electrode. 7. The time-independent (background) current was obtained by subtracting the gated channel current from the steady-state I-V curve. This current also rectified in the inward direction. 8. The inwardly rectifying I-V relations were theoretically described by a channel having a row of ion-selective sites along which ions move in a single file (Hodgkin & Keynes, 1955), and a membrane-bound particle which blocked the channel in a voltage-dependent manner. 9. The relationship of the voltage-clamp results to spontaneous activity is discussed and comparisons are made with measurements from whole embryonic heart and other cardiac tissues.
摘要
  1. 从7日龄鸡胚心脏心室解离的小细胞团聚体,在低钾浓度(Ko = 1.3 mM)的组织培养基中能自发搏动。向外部培养基中添加河豚毒素(TTX)或钾离子可阻断此活动。2. 采用双微电极电压钳技术分析负责起搏去极化的阈下电流。3. 持续6 - 10秒的电压钳步阶显示出具有一级动力学的时间依赖性电流。其稳态激活的膜电位范围为 - 90至 - 60 mV。4. 该电流动力学在定性上与霍奇金和赫胥黎(1952b)的相似,在V = - 75 mV时峰值时间常数约为1秒。动力学与Ko无关。5. 时间依赖性电流归因于门控膜通道。按照诺布尔和钱恩(1968)的程序,通过电压钳步阶期间和之后时间依赖性电流幅度的比值来确定通道的完全激活电流 - 电压(I - V)关系。6. 完全激活的I - V关系在比其反转电位正15 mV以上的电位处显示出内向整流,负斜率电导。Ko的变化使I - V曲线沿电压轴移动,如同钾电极一样。7. 通过从稳态I - V曲线中减去门控通道电流获得时间无关(背景)电流。该电流也向内整流。8. 内向整流的I - V关系在理论上由一个具有一排离子选择位点的通道来描述,离子沿此单排移动(霍奇金和凯恩斯,1955),以及一个以电压依赖性方式阻断通道的膜结合颗粒。9. 讨论了电压钳结果与自发活动的关系,并与整个胚胎心脏和其他心脏组织的测量结果进行了比较。

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