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单个心肌细胞中游离钙的水母发光蛋白测量法

Aequorin measurements of free calcium in single heart cells.

作者信息

Cobbold P H, Bourne P K

出版信息

Nature. 1984;312(5993):444-6. doi: 10.1038/312444a0.

Abstract

The performance of the heart depends on the concentrations of free calcium ions in the cytoplasm of the myocytes. However, direct evidence for changes in free Ca concentration in physiological events during response to drugs and in pathogenesis has been difficult to obtain because of technical problems in measuring free Ca at 10(-7) M in cells with a volume of only a few picolitres. Here we describe measurements made with the Ca-sensitive photoprotein aequorin in single ventricular myocytes isolated from rat heart. We have detected signals from resting and contracting cells, and from cells exposed to media of altered ionic composition (raised K, lowered Na), ouabain and metabolic inhibitors. We report that free Ca in metabolically-poisoned myocytes is remarkably stable and that severe injury to the cell occurs before the free Ca concentration rises above 1-3 X 10(-7) M, hence cell damage seems to be a cause, not a consequence, of a rise in free Ca. The technique used here should help to resolve many uncertainties regarding free Ca in heart function, and should be particularly valuable for investigating the role of free Ca in ischaemic pathogenesis.

摘要

心脏的功能取决于心肌细胞质中游离钙离子的浓度。然而,由于在仅几皮升体积的细胞中测量10^(-7)M游离钙存在技术问题,很难获得药物反应和发病机制等生理事件中游离钙浓度变化的直接证据。在此,我们描述了用对钙敏感的光蛋白水母发光蛋白对从大鼠心脏分离的单个心室肌细胞进行的测量。我们检测到了静息和收缩细胞以及暴露于离子组成改变(钾升高、钠降低)的培养基、哇巴因和代谢抑制剂的细胞发出的信号。我们报告,代谢中毒的心肌细胞中的游离钙非常稳定,并且在游离钙浓度升高到1 - 3×10^(-7)M以上之前,细胞就会发生严重损伤,因此细胞损伤似乎是游离钙升高的原因,而非结果。这里使用的技术应有助于解决许多关于心脏功能中游离钙的不确定性问题,并且对于研究游离钙在缺血发病机制中的作用尤其有价值。

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