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电刺激可防止类固醇去神经大鼠骨骼肌肌球蛋白的选择性丢失。

Electrical Stimulation Prevents Preferential Skeletal Muscle Myosin Loss in Steroid-Denervation Rats.

作者信息

Yamada Takashi, Himori Koichi, Tatebayashi Daisuke, Yamada Ryotaro, Ashida Yuki, Imai Tomihiro, Akatsuka Masayuki, Masuda Yoshiki, Kanzaki Keita, Watanabe Daiki, Wada Masanobu, Westerblad Håkan, Lanner Johanna T

机构信息

Graduate School of Health Sciences, Sapporo Medical University, Sapporo, Japan.

Department of Intensive Care Medicine, Sapporo Medical University, Sapporo, Japan.

出版信息

Front Physiol. 2018 Aug 10;9:1111. doi: 10.3389/fphys.2018.01111. eCollection 2018.

Abstract

Severe muscle weakness concomitant with preferential depletion of myosin has been observed in several pathological conditions. Here, we used the steroid-denervation (S-D) rat model, which shows dramatic decrease in myosin content and force production, to test whether electrical stimulation (ES) treatment can prevent these deleterious changes. S-D was induced by cutting the sciatic nerve and subsequent daily injection of dexamethasone for 7 days. For ES treatment, plantarflexor muscles were electrically stimulated to produce four sets of five isometric contractions each day. Plantarflexor isometric torque, muscle weight, skinned muscle fiber force, and protein and mRNA expression were measured after the intervention period. ES treatment partly prevented the S-D-induced decreases in plantarflexor isometric torque and muscle weight. ES treatment fully prevented S-D-induced decreases in skinned fiber force and ratio of myosin heavy chain (MyHC) to actin, as well as increases in the reactive oxygen/nitrogen species-generating enzymes NADPH oxidase (NOX) 2 and 4, phosphorylation of p38 MAPK, mRNA expression of the muscle-specific ubiquitin ligases muscle ring finger-1 (MuRF-1) and atrogin-1, and autolyzed active calpain-1. Thus, ES treatment is an effective way to prevent muscle impairments associated with loss of myosin.

摘要

在几种病理状况下已观察到严重肌无力并伴有肌球蛋白的优先耗竭。在此,我们使用类固醇去神经支配(S-D)大鼠模型(该模型显示肌球蛋白含量和力量产生显著下降)来测试电刺激(ES)治疗是否能预防这些有害变化。通过切断坐骨神经并随后每日注射地塞米松7天来诱导S-D。对于ES治疗,每天对跖屈肌进行电刺激以产生四组每组五次的等长收缩。在干预期后测量跖屈肌等长扭矩、肌肉重量、脱皮肤肌纤维力量以及蛋白质和mRNA表达。ES治疗部分预防了S-D诱导的跖屈肌等长扭矩和肌肉重量的下降。ES治疗完全预防了S-D诱导的脱皮肤纤维力量以及肌球蛋白重链(MyHC)与肌动蛋白比率的下降,以及活性氧/氮物种生成酶NADPH氧化酶(NOX)2和4、p38 MAPK磷酸化、肌肉特异性泛素连接酶肌肉环指蛋白-1(MuRF-1)和atrogin-1的mRNA表达以及自溶活性钙蛋白酶-1的增加。因此,ES治疗是预防与肌球蛋白丧失相关的肌肉损伤的有效方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c53/6097132/df44c4da0e2b/fphys-09-01111-g001.jpg

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