Suppr超能文献

2,3-丁二酮单肟对青蛙骨骼肌纤维收缩的作用机制

Mechanism of action of 2, 3-butanedione 2-monoxime on contraction of frog skeletal muscle fibres.

作者信息

Horiuti K, Higuchi H, Umazume Y, Konishi M, Okazaki O, Kurihara S

机构信息

Department of Physiology, Jikei University School of Medicine, Tokyo, Japan.

出版信息

J Muscle Res Cell Motil. 1988 Apr;9(2):156-64. doi: 10.1007/BF01773737.

Abstract

The mechanism of the inhibitory effect of 2,3-butanedione 2-monoxime (BDM) on contraction of frog skeletal muscles was studied using skinned fibres and aequorin-injected intact fibres. The tension development of skinned fibres directly activated with calcium was strongly inhibited by BDM. This agent also had effects on the sarcoplasmic reticulum in the skinned preparations, suppressing the calcium pump function and enhancing the activity of the 'calcium-induced calcium release' mechanism. In electrically stimulated intact fibres, although BDM slightly suppressed the elevation of the intracellular calcium ion concentration, this effect was so weak that it would not explain the strong inhibitory effect of the agent on the tension development by the intact fibres. It was concluded that the tension reducing effect of BDM on intact fibres was due mainly to its direct action on the contractile system. The mode of this action of BDM was further examined with skinned fibres in view of its effects on the maximum shortening speed and isometric tension in low MgATP environments.

摘要

利用去皮肤纤维和注射水母发光蛋白的完整纤维,研究了2,3 - 丁二酮单肟(BDM)对青蛙骨骼肌收缩的抑制作用机制。用钙直接激活的去皮肤纤维的张力发展受到BDM的强烈抑制。该试剂对去皮肤制剂中的肌浆网也有影响,抑制钙泵功能并增强“钙诱导钙释放”机制的活性。在电刺激的完整纤维中,尽管BDM略微抑制了细胞内钙离子浓度的升高,但这种作用非常微弱,无法解释该试剂对完整纤维张力发展的强烈抑制作用。得出的结论是,BDM对完整纤维的张力降低作用主要是由于其对收缩系统的直接作用。鉴于BDM在低MgATP环境中对最大缩短速度和等长张力的影响,用去皮肤纤维进一步研究了其这种作用方式。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验