• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[强直收缩过程中机电活动的变化]

[Changes in the electromechanical activity in the course of tetanic contraction].

作者信息

Nasledov G A, Katina I E, Zhitnikova Iu V

出版信息

Ross Fiziol Zh Im I M Sechenova. 2005 Nov;91(11):1288-98.

PMID:16408637
Abstract

The functioning of excitation-contraction coupling during tetanic contraction was investigated on frog skeletal muscle. The effect of the calcium release blocker dantrolene was tested on electrically evoked twitches and tetanic contractions. It was shown that the first: developmental stage of tetanus is inhibited by dantrolene as well as a twitch contraction, and does not influenced by calcium-free medium. This substantiates it as based on "voltage dependent Ca-release" (VDCR) mechanism of activation, when depolarization directly opens the rhyanodin receptor calcium channels. The next stage: the long lasting plateau of tetanic contraction, is directly dependent on external Ca2+ entry and also inhibited by dantrolene, and therefore may be described as "calcium-induced Ca-release" (CICR) activation mechanism. It is proposed that such change in ECC mechanism taking place during tetanic contraction, can occur also in conditions of natural muscle activity, because of its rhythmical nature.

摘要

在青蛙骨骼肌上研究了强直收缩期间兴奋-收缩偶联的功能。测试了钙释放阻滞剂丹曲林对电诱发的单收缩和强直收缩的影响。结果表明:破伤风的第一个发育阶段以及单收缩均受丹曲林抑制,且不受无钙培养基影响。这证实其基于“电压依赖性钙释放”(VDCR)激活机制,即去极化直接打开兰尼碱受体钙通道。下一阶段:强直收缩的持久平台期,直接依赖于细胞外Ca2+内流,也受丹曲林抑制,因此可描述为“钙诱导钙释放”(CICR)激活机制。有人提出,强直收缩期间发生的这种兴奋-收缩偶联机制变化,由于其节律性,在自然肌肉活动条件下也可能发生。

相似文献

1
[Changes in the electromechanical activity in the course of tetanic contraction].[强直收缩过程中机电活动的变化]
Ross Fiziol Zh Im I M Sechenova. 2005 Nov;91(11):1288-98.
2
[Functioning of the electromechanical connection in the course of the contracture contraction].[挛缩收缩过程中机电连接的功能]
Ross Fiziol Zh Im I M Sechenova. 2004 Mar;90(3):327-38.
3
Changes in the functioning of the electromechanical connection during tetanic contraction.强直收缩期间机电连接功能的变化。
Neurosci Behav Physiol. 2007 Feb;37(2):153-9. doi: 10.1007/s11055-007-0163-8.
4
Effects of dantrolene on steps of excitation-contraction coupling in mammalian skeletal muscle fibers.丹曲林对哺乳动物骨骼肌纤维兴奋-收缩偶联步骤的影响。
J Gen Physiol. 2001 Oct;118(4):355-75. doi: 10.1085/jgp.118.4.355.
5
[Characteristics of functioning of electromechanical coupling in striated muscles of higher and lower vertebrates].[高等和低等脊椎动物横纹肌中机电耦合的功能特性]
Biofizika. 2002 Jul-Aug;47(4):716-27.
6
Effects of dantrolene and its derivatives on Ca(2+) release from the sarcoplasmic reticulum of mouse skeletal muscle fibres.丹曲林及其衍生物对小鼠骨骼肌纤维肌浆网Ca(2+)释放的影响。
Br J Pharmacol. 2001 Oct;134(4):729-36. doi: 10.1038/sj.bjp.0704307.
7
[Effects of agonists and antagonists of rhyanodine receptors on potassium contractures in twitch and tonic frog skeletal muscle fibers].[兰尼碱受体激动剂和拮抗剂对青蛙抽搐和强直骨骼肌纤维钾挛缩的影响]
Biofizika. 2006 Sep-Oct;51(5):898-905.
8
Membrane depolarization increases ryanodine sensitivity to Ca2+ release to the cytosol in L6 skeletal muscle cells: Implications for excitation-contraction coupling.膜去极化增加了L6骨骼肌细胞中兰尼碱对Ca2+释放到细胞质的敏感性:对兴奋-收缩偶联的影响。
Exp Biol Med (Maywood). 2016 Apr;241(8):854-62. doi: 10.1177/1535370215619706. Epub 2015 Dec 6.
9
Effects of ryanodine receptor agonist 4-chloro-m-cresol on myoplasmic free Ca2+ concentration and force of contraction in mouse skeletal muscle.兰尼碱受体激动剂4-氯间甲酚对小鼠骨骼肌肌浆游离钙离子浓度及收缩力的影响
Cell Calcium. 1998 Aug;24(2):105-15. doi: 10.1016/s0143-4160(98)90078-1.
10
A surface potential change in the membranes of frog skeletal muscle is associated with excitation-contraction coupling.青蛙骨骼肌细胞膜上的表面电位变化与兴奋-收缩偶联相关。
J Physiol. 1997 Mar 15;499 ( Pt 3)(Pt 3):787-808. doi: 10.1113/jphysiol.1997.sp021969.