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缩短诱导的青蛙和小鼠横纹肌皮肤纤维失活。

Shortening induced deactivation of skinned fibres of frog and mouse striated muscle.

作者信息

Ekelund M C, Edman K A

出版信息

Acta Physiol Scand. 1982 Oct;116(2):189-99. doi: 10.1111/j.1748-1716.1982.tb07129.x.

Abstract

The depressant effect of active shortening, previously established in intact muscle fibres, was studied during calcium induced contractures of chemically skinned fibres from the semitendinosus muscle of Rana temporaria and the psoas muscle of the mouse. The decrease in contractile activity was determined by comparing the rate of force redevelopment (at a given tension level) after a large (test) and a small (control) release step. Under standard experimental conditions (ionic strength: frog 135 mM, mouse 190 mM; Ca2+ 3.0 microM; Mg2+: frog 25 microM, mouse 100 microM; MgATP2-: frog 1.0 mM, mouse 2.0 mM) active shortening of 0.15 microns per sarcomere (in excess of control release) reduced the contractile activity by approximately 50% of the control in both frog and mouse muscle fibres. Full contractile activity was regained within less than 4 s during isometric activity after the shortening phase. The depressant effect of shortening was steadily reduced, to almost complete disappearance of the effect, by increasing the free calcium concentration within the range 1.5-12.0 microM. Similarly, an increase in ionic strength from 105 to 235 mM reduced the depressant effect by approximately 40%. In contrast, there was a progressive enhancement of the shortening effect as the magnesium ion concentration was increased from 25 to 590 microM. It is proposed that interaction between the myosin cross-bridges and the thin filament during sarcomere shortening leads to a decrease in troponin-calcium binding resulting in a temporary deactivation of the contractile system.

摘要

先前在完整肌纤维中确定的主动缩短的抑制作用,在钙诱导的来自林蛙半腱肌和小鼠腰大肌的化学去膜纤维挛缩过程中进行了研究。通过比较大(测试)和小(对照)释放步骤后(在给定张力水平下)力重新发展的速率来确定收缩活性的降低。在标准实验条件下(离子强度:青蛙135 mM,小鼠190 mM;Ca2+ 3.0 microM;Mg2+:青蛙25 microM,小鼠100 microM;MgATP2-:青蛙1.0 mM,小鼠2.0 mM),每个肌节主动缩短0.15微米(超过对照释放)使青蛙和小鼠肌纤维的收缩活性降低至对照的约50%。在缩短阶段后的等长活动期间,不到4秒内即可恢复完全收缩活性。通过将游离钙浓度在1.5 - 12.0 microM范围内增加,缩短的抑制作用稳步降低,直至该作用几乎完全消失。同样,离子强度从105 mM增加到235 mM使抑制作用降低了约40%。相反,随着镁离子浓度从25 microM增加到590 microM,缩短作用逐渐增强。有人提出,肌节缩短过程中肌球蛋白横桥与细肌丝之间的相互作用导致肌钙蛋白 - 钙结合减少,从而导致收缩系统暂时失活。

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