首页> 外文会议>Proceedings of International Kunming Symposium on Microscopy July 2-5, 2000 Kunming, Yunnan Province, China >Ca~(2+) concentration changes in SR during skeletal muscular excitation -contraction coupling
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Ca~(2+) concentration changes in SR during skeletal muscular excitation -contraction coupling

机译:Ca〜(2+)浓度在骨骼肌兴奋-收缩耦合过程中的变化

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How is ultrastructural change at millisecond time course in skeletal muscle during coupling after electrical stimulation? What is the relationship between structural change and functional change as excitation-contraction coupling was conducted in skeletal muscle? Though the problems have been studied physiologically for long time, there are still in indistinction. The cause is that the muscular structural change is very fast (millisecond state) during coupling. So it can not be realized that the skeletal muscles are immediately fixed by chemical fixation during coupling. To solve the problems, the ideal method is the freezing fixation and computer technology. We employ a new technology that is the system of a detector with two-way infrared and a computer in order to control the signal ofelectrical stimulation and quick-freezing fixation for structural researches of skeletal muscle during excitation-contraction coupling. The purpose is that skeletal muscle is immediately fixed by quick freezing after electrical stimulation following the known time courses. So it is possible for us to understand the ultrastructural change of skeletal muscle through our tests. We have obtained the ultrastructure and Ca~(2+) concentration changes of skeletal muscle in 0.8 ms and 5.6 ms after electrical stimulation.
机译:电刺激后耦合过程中骨骼肌在毫秒时间过程中的超微结构如何变化?在骨骼肌中进行兴奋收缩耦合后,结构变化与功能变化之间有什么关系?尽管对这些问题进行了长期的生理研究,但仍然存在歧义。原因是在耦合过程中,肌肉的结构变化非常快(毫秒状态)。因此,无法认识到在耦合过程中骨骼肌立即被化学固定所固定。为了解决这些问题,理想的方法是冷冻固定和计算机技术。我们采用一种新技术,即具有双向红外检测器和计算机的系统,以控制电刺激和速冻固定的信号,用于骨骼肌肉在激发-收缩耦合过程中的结构研究。目的是在遵循已知的时程后,在电刺激后通过快速冷冻立即固定骨骼肌。因此,我们可以通过测试了解骨骼肌的超微结构变化。我们获得了电刺激后0.8 ms和5.6 ms内骨骼肌的超微结构和Ca〜(2+)浓度变化。

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