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二氢吡啶受体正向信号增加体内大鼠快肌重复收缩后的钙漏。

Orthograde signal of dihydropyridine receptor increases Ca leakage after repeated contractions in rat fast-twitch muscles in vivo.

机构信息

Graduate School of Humanities and Social Sciences, Hiroshima University, Hiroshima, Japan.

出版信息

Am J Physiol Cell Physiol. 2021 May 1;320(5):C806-C821. doi: 10.1152/ajpcell.00364.2020. Epub 2021 Feb 17.

DOI:10.1152/ajpcell.00364.2020
PMID:33596151
Abstract

The purpose of this study was to investigate the mechanism underlying sarcoplasmic reticulum (SR) Ca leakage after in vivo contractions. Rat gastrocnemius muscles were electrically stimulated in vivo, and then mechanically skinned fibers and SR microsomes were prepared from the muscles excised 30 min after repeated high-intensity contractions. The mechanically skinned fibers maintained the interaction between dihydropyridine receptors (DHPRs) and ryanodine receptors (RyRs), whereas the SR microsomes did not. Interestingly, skinned fibers from the stimulated muscles showed increased SR Ca leakage, whereas Ca leakage decreased in SR microsomes from the stimulated muscles. To enhance the orthograde signal of DHPRs, SR Ca leakage in the skinned fiber was measured ) under a continuously depolarized condition and ) in the presence of nifedipine. As a result, in either of the two conditions, SR Ca leakage in the rested fibers reached a level similar to that in the stimulated fibers. Furthermore, the increased SR Ca leakage from the stimulated fibers was alleviated by treatment with 1 mM tetracaine (Tet) but not by treatment with 3 mM free Mg (3 Mg). Tet exerted a greater inhibitory effect on the DHPR signal to RyR than 3 Mg, although their inhibitory effects on RyR were almost similar. These results suggest that the increased Ca leakage after muscle contractions is mainly caused by the orthograde signal of DHPRs to RyRs.

摘要

本研究旨在探讨肌浆网(SR)Ca 渗漏的机制。通过体内电刺激大鼠比目鱼肌,在重复高强度收缩后 30 分钟切除肌肉,制备机械去神经纤维和 SR 微粒体。机械去神经纤维保持二氢吡啶受体(DHPRs)和兰尼碱受体(RyRs)之间的相互作用,而 SR 微粒体则没有。有趣的是,刺激肌肉的去神经纤维表现出增加的 SR Ca 渗漏,而刺激肌肉的 SR 微粒体中的 Ca 渗漏减少。为了增强 DHPRs 的顺行信号,在持续去极化条件下测量了去神经纤维中的 SR Ca 渗漏,)在硝苯地平存在下。结果,在这两种情况下,休息纤维中的 SR Ca 渗漏达到与刺激纤维相似的水平。此外,用 1 mM 四卡因(Tet)处理可减轻刺激纤维中增加的 SR Ca 渗漏,但用 3 mM 游离 Mg(3Mg)处理则不能。Tet 对 DHPR 信号到 RyR 的抑制作用大于 3Mg,尽管它们对 RyR 的抑制作用几乎相似。这些结果表明,肌肉收缩后 Ca 渗漏的增加主要是由 DHPRs 对 RyRs 的顺行信号引起的。

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Ryanodine receptor leak triggers fiber Ca redistribution to preserve force and elevate basal metabolism in skeletal muscle.兰尼碱受体泄漏引发肌纤维钙重新分布,以维持骨骼肌力量并提高基础代谢。
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