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电压钳制的青蛙心室肌细胞外钾离子蓄积

Extracellular potassium accumulation in voltage-clamped frog ventricular muscle.

作者信息

Cleemann L, Morad M

出版信息

J Physiol. 1979 Jan;286:83-111. doi: 10.1113/jphysiol.1979.sp012608.

Abstract
  1. Application of voltage clamp pulses (1--10 sec) to frog ventricular strips causes temporary changes in the extracellular K concentration. 2. The changes in the extracellular K concentration can be estimated from (a) slowly decaying post-clamp after-potentials, (b) changes in the action potential duration, and (c) measurements with a K-selective micro-electrode. 3. The depolarization of the resting potential and the shortening of the action potential are present in approximately the same proportions during voltage-clamp induced extracellular K accumulation and during perfusion with a K-ricn Ringer solution but small consistent differences are noticed. 4. The measurements of the after-potential, the action potential shortening, and the K-electrode response were analysed as indicators of extracellular K+ activity and it was concluded that the after-potential provides the most convenient and reliable estimate of the absolute magnitude of the voltage-clamp induced extracellular K accumulation. 5. The depolarizing after-potentials decay more slowly than the hyperpolarizing after-potentials but it is found that this reflects the selectivity of the membrane to K+ concentrations as predicted by the Nernst or the Goldman equations. 6. Analysis of the redistribution of accumulated K+ from the decay of the after-potential suggests that the major part of the redistribution process can be described by a single time constant (2--4 sec). A much longer time constant is required for a smaller component of the 'tail' in order to bring [K]o to the normal resting state. 7. N-shaped relations similar to the 'steady state' current-voltage relation are obtained when the post-clamp after-potential, the action potential shortening, and the K-electrode response are plotted versus the clamped membrane potential. The maxima of these curves are located around -40 mV and the minima around -20 mV. 8. In spite of a significant outward membrane current (1--1.5 microamperemeter) in the minimum region (-20 mV), the post-clamp after-potential is often hyperpolarizing in nature suggesting extracellular K depletion. 9. These findings indicate that the K efflux is lower at -20 mV than at both higher and lower potentials and suggest that the N-shape 'steady state' current-voltage relation mainly reflects the voltage dependency of the K current. 10. A theory for K accumulation in a single compartment is presented which predicts that a simple linear RC-circuit may describe the electrical response of the preparation in a limited potential range around the resting potential. The extracellular accumulation space was estimated to be 13--16% of the total volume of the preparation. It is tentatively suggested that the accumulation space is equivalent to the subendothelial fraction of the extracellular space.
摘要
  1. 对蛙心室肌条施加电压钳脉冲(1 - 10秒)会导致细胞外钾浓度发生暂时变化。2. 细胞外钾浓度的变化可通过以下方式估算:(a)钳制后缓慢衰减的后电位,(b)动作电位时程的变化,以及(c)用钾选择性微电极进行测量。3. 在电压钳诱导的细胞外钾积累过程中以及用富含钾的林格液灌注时,静息电位的去极化和动作电位的缩短出现的比例大致相同,但存在一些小的一致性差异。4. 对后电位、动作电位缩短和钾电极反应的测量作为细胞外钾离子活性的指标进行了分析,得出的结论是,后电位为电压钳诱导的细胞外钾积累的绝对量提供了最方便可靠的估计。5. 去极化后电位的衰减比超极化后电位慢,但发现这反映了膜对钾离子浓度的选择性,正如能斯特或戈德曼方程所预测的那样。6. 对后电位衰减过程中积累的钾离子再分布的分析表明,再分布过程的主要部分可用单个时间常数(2 - 4秒)来描述。为使细胞外钾浓度恢复到正常静息状态,“尾”部较小部分需要更长的时间常数。7. 当将钳制后电位、动作电位缩短和钾电极反应与钳制膜电位作图时,可得到类似于“稳态”电流 - 电压关系的N形关系。这些曲线的最大值位于约 - 40 mV附近,最小值位于约 - 20 mV附近。8. 尽管在最小区域( - 20 mV)存在显著的外向膜电流(1 - 1.5微安),钳制后电位在性质上通常是超极化的,表明细胞外钾离子减少。9. 这些发现表明,在 - 20 mV时钾离子外流比在更高和更低电位时都低,这表明N形“稳态”电流 - 电压关系主要反映了钾电流的电压依赖性。10. 提出了一个单室中钾积累的理论,该理论预测,一个简单的线性RC电路可以描述在静息电位周围有限电位范围内标本的电反应。细胞外积累空间估计为标本总体积的13 - 16%。初步认为积累空间相当于细胞外空间的内皮下部分。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ab/1281560/a2a2ae61394e/jphysiol00755-0097-a.jpg

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