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电压钳制、内部灌注的单个心肌细胞的收缩。

Contraction in voltage-clamped, internally perfused single heart cells.

作者信息

London B, Krueger J W

出版信息

J Gen Physiol. 1986 Oct;88(4):475-505. doi: 10.1085/jgp.88.4.475.

Abstract

We studied contraction in single voltage-clamped, internally perfused myocytes isolated from guinea pig ventricles. The microscopic appearance of the cell was observed and recorded with a television system, while contractile shortening was measured 1,000 times/s using a linear photodiode array. Uniform, synchronous sarcomere shortening occurred in response to depolarizations that triggered a slow inward current (Isi). Changes in Isi caused by altering the amplitude of the voltage step, the extracellular [Ca2+], or the holding potential were accompanied by immediate parallel changes in the extent and velocity of shortening. In particular, twitch shortening during depolarization was immediately decreased when large voltage steps decreased Isi, and was eliminated by depolarizations that exceeded +75 mV, the apparent reversal potential for Ca2+. In these cases, shortening was associated with the tail current during repolarization. Increases in the amplitude, duration, and the rate of the depolarizing step increased the extent and speed of sarcomere shortening over the course of four to five contractions without a simultaneous parallel increase of Isi. Large prolonged depolarizations caused an asynchronous, nonuniform, oscillatory shortening of the cell and potentiated future twitch contractions. Increases in the duration of the depolarizing step immediately prolonged contraction; otherwise, interventions that altered the extent, velocity, and time course of shortening in intact, nonperfused cells did not affect the time course of the contraction in the internally perfused single cells. Our results provide direct support for the hypothesis that Isi both induces and grades the size of the Ca2+ release from the sarcoplasmic reticulum of intact cardiac muscle. In addition, a separate, depolarization-dependent process unrelated to Isi grades the size of contraction, presumably by modulating Ca2+ accumulation in the intracellular stores, and affects its time course.

摘要

我们研究了从豚鼠心室分离出的单个电压钳制、内部灌注的心肌细胞的收缩情况。用电视系统观察并记录细胞的微观形态,同时使用线性光电二极管阵列以每秒1000次的频率测量收缩性缩短。对引发缓慢内向电流(Isi)的去极化反应,肌节发生均匀、同步的缩短。通过改变电压阶跃幅度、细胞外[Ca2+]或钳制电位引起的Isi变化,伴随着缩短程度和速度的立即平行变化。特别是,当大电压阶跃降低Isi时,去极化期间的单收缩缩短立即减少,并且超过+75 mV(Ca2+的表观反转电位)的去极化会消除这种缩短。在这些情况下,缩短与复极化期间的尾电流相关。去极化步骤的幅度、持续时间和速率增加,在四到五次收缩过程中增加了肌节缩短的程度和速度,而没有同时平行增加Isi。大的长时间去极化导致细胞异步、不均匀、振荡性缩短,并增强未来的单收缩。去极化步骤持续时间的增加立即延长收缩;否则,改变完整、未灌注细胞中缩短的程度、速度和时间进程的干预措施不会影响内部灌注的单个细胞中的收缩时间进程。我们的结果为以下假设提供了直接支持:Isi既诱导又分级调节完整心肌肌浆网中Ca2+释放的大小。此外,一个与Isi无关的、依赖去极化的单独过程分级调节收缩大小,大概是通过调节细胞内储存中Ca2+的积累,并影响其时间进程。

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