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肌浆网钙释放通道(雷诺丁受体)活性调节、肌肉疲劳和谢韦尔金现象的分子机制。

Molecular mechanisms of regulation of the activity of sarcoplasmic reticulum Ca-release channels (ryanodine receptors), muscle fatigue, and Severin's phenomenon.

作者信息

Rubtsov A M

机构信息

Department of Biochemistry, School of Biology, Lomonosov Moscow State University, Moscow, 119899, Russia.

出版信息

Biochemistry (Mosc). 2001 Oct;66(10):1132-43. doi: 10.1023/a:1012485030527.

Abstract

In this short review of the literature and our own data the characteristics of structural organization of sarcoplasmic reticulum Ca-release channels (ryanodine receptors) in different types of muscles, the participation of other sarcoplasmic reticulum proteins in excitation-contraction coupling and Ca-release channel operation, and the regulation of the channel activity by endogenous low molecular weight compounds are analyzed. Special attention is given to changes that occur in muscle cells during exhausting work and to the role of sarcoplasmic reticulum Ca-release channels in the loss of muscle contractile activity during the development of fatigue. It is concluded that the protection of muscle fibers against fatigue in the presence of the histidine-containing dipeptide carnosine, called in the literature "Severin's phenomenon", is primarily connected with modulation of sarcoplasmic reticulum Ca-release channel activity by carnosine.

摘要

在这篇对文献及我们自身数据的简短综述中,分析了不同类型肌肉中肌浆网钙释放通道(雷诺丁受体)的结构组织特征、其他肌浆网蛋白在兴奋-收缩偶联及钙释放通道运作中的参与情况,以及内源性低分子量化合物对通道活性的调节。特别关注了疲劳性工作期间肌肉细胞中发生的变化,以及肌浆网钙释放通道在疲劳发展过程中肌肉收缩活性丧失中的作用。得出的结论是,在文献中被称为“谢韦林现象”的含组氨酸二肽肌肽存在时,肌肉纤维对疲劳的保护主要与肌肽对肌浆网钙释放通道活性的调节有关。

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