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蛙骨骼肌兴奋-收缩偶联中的钙

Calcium in excitation--contraction coupling of frog skeletal muscle.

作者信息

Taylor S R, Lopez J R, Griffiths P J, Trube G, Cecchi G

出版信息

Can J Physiol Pharmacol. 1982 Apr;60(4):489-502. doi: 10.1139/y82-068.

Abstract

A principal step in the process leading to muscle contraction is the intracellular release of Ca2+. We have detected and compared some physical and chemical events that reflect Ca2+ release in contracting frog skeletal muscle cells, described the effects of some agents that are believed to alter intracellular Ca2+ release during contraction, and speculated about the role of Ca2+ release in influencing some of the mechanical properties of frog muscle. The specific physical features recorded were changes in striation spacing, myofibrillar orientation, and force development. The chemical feature was the relative change in intracellular [Ca2+] recorded as light emission from cells microinjected with the Ca2+-sensitive protein aequorin. The presence or absence of a correlation among these variables has been used (i) to evaluate the action of some agents thought to change intracellular Ca2+ release in excitation--contraction (E--C) coupling, (ii) to further substantiate the effects of cell length on Ca2+ release, and (iii) to examine some details of models for E--C coupling. The results showed that potentiating agents enhance and prolong intracellular Ca2+ release without changing the rate of Ca2+ removal during E--C coupling. This extra Ca2+ does not produce the same effect on contractions at all lengths. Contractility is inversely related to cell length, and Ca2+-induced activation is normally less than maximum not only at short lengths but also at optimal striation spacings.

摘要

导致肌肉收缩过程中的一个主要步骤是细胞内Ca2+的释放。我们检测并比较了一些反映收缩中的青蛙骨骼肌细胞内Ca2+释放的物理和化学事件,描述了一些据信在收缩过程中改变细胞内Ca2+释放的试剂的作用,并推测了Ca2+释放在影响青蛙肌肉某些力学特性中的作用。记录的具体物理特征是条纹间距、肌原纤维取向和力发展的变化。化学特征是记录为微注射Ca2+敏感蛋白水母发光蛋白的细胞发出的光的细胞内[Ca2+]的相对变化。这些变量之间是否存在相关性已被用于:(i)评估一些被认为在兴奋-收缩(E-C)偶联中改变细胞内Ca2+释放的试剂的作用;(ii)进一步证实细胞长度对Ca2+释放的影响;(iii)研究E-C偶联模型的一些细节。结果表明,增强剂在E-C偶联过程中增强并延长细胞内Ca2+释放,而不改变Ca2+清除率。这种额外的Ca2+在所有长度下对收缩的影响并不相同。收缩性与细胞长度成反比,并且Ca2+诱导的激活不仅在短长度下,而且在最佳条纹间距下通常都小于最大值。

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