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血流限制、低强度等长电刺激引起大鼠比目鱼肌肥大:肌肉缺氧的作用。

Muscle hypertrophy following blood flow-restricted, low-force isometric electrical stimulation in rat tibialis anterior: role for muscle hypoxia.

机构信息

Department of Cardiovascular Medicine, Dokkyo Medical University and Heart Center, Dokkyo Medical University Hospital , Tochigi , Japan.

Bioscience and Technology Program, Department of Engineering Science, University of Electro-Communications , Tokyo , Japan.

出版信息

J Appl Physiol (1985). 2018 Jul 1;125(1):134-145. doi: 10.1152/japplphysiol.00972.2017. Epub 2018 Mar 22.

DOI:10.1152/japplphysiol.00972.2017
PMID:29565774
Abstract

Low-force exercise training with blood flow restriction (BFR) elicits muscle hypertrophy as seen typically after higher-force exercise. We investigated the effects of microvascular hypoxia [i.e., low microvascular O partial pressures (P mvO)] during contractions on muscle hypertrophic signaling, growth response, and key muscle adaptations for increasing exercise capacity. Wistar rats were fitted with a cuff placed around the upper thigh and inflated to restrict limb blood flow. Low-force isometric contractions (30 Hz) were evoked via electrical stimulation of the tibialis anterior (TA) muscle. The P mvO was determined by phosphorescence quenching. Rats underwent acute and chronic stimulation protocols. Whereas P mvO decreased transiently with 30 Hz contractions, simultaneous BFR induced severe hypoxia, reducing P mvO lower than present for maximal (100 Hz) contractions. Low-force electrical stimulation (EXER) induced muscle hypertrophy (6.2%, P < 0.01), whereas control group conditions or BFR alone did not. EXER+BFR also induced an increase in muscle mass (11.0%, P < 0.01) and, unique among conditions studied, significantly increased fiber cross-sectional area in the superficial TA ( P < 0.05). Phosphorylation of ribosomal protein S6 was enhanced by EXER+BFR, as were peroxisome proliferator-activated receptor gamma coactivator-1α and glucose transporter 4 protein levels. Fibronectin type III domain-containing protein 5, cytochrome c oxidase subunit 4, monocarboxylate transporter 1 (MCT1), and cluster of differentiation 147 increased with EXER alone. EXER+BFR significantly increased MCT1 expression more than EXER alone. These data demonstrate that microvascular hypoxia during contractions is not essential for hypertrophy. However, hypoxia induced via BFR may potentiate the muscle hypertrophic response (as evidenced by the increased superficial fiber cross-sectional area) with increased glucose transporter and mitochondrial biogenesis, which contributes to the pleiotropic effects of exercise training with BFR that culminate in an improved capacity for sustained exercise. NEW & NOTEWORTHY We investigated the effects of low microvascular O partial pressures (P mvO) during contractions on muscle hypertrophic signaling and key elements in the muscle adaptation for increasing exercise capacity. Although demonstrating that muscle hypoxia is not obligatory for the hypertrophic response to low-force, electrically induced muscle contractions, the reduced P mvO enhanced ribosomal protein S6 phosphorylation and potentiated the hypertrophic response. Furthermore, contractions with blood flow restriction increased oxidative capacity, glucose transporter, and mitochondrial biogenesis, which are key determinants of the pleiotropic effects of exercise training.

摘要

低强度力量训练结合血流限制(BFR)可引起肌肉肥大,其效果类似于高强度力量训练后的效果。我们研究了收缩过程中微血管缺氧(即低微血管氧分压(PmvO))对肌肉肥大信号、生长反应以及增加运动能力的关键肌肉适应的影响。我们将 Wistar 大鼠的大腿上部套上一个袖带并充气,以限制肢体血液流动。通过电刺激胫骨前肌(TA)来引发低强度等长收缩(30 Hz)。通过磷光猝灭法测定 PmvO。大鼠接受了急性和慢性刺激方案。虽然 30 Hz 收缩会导致 PmvO 短暂下降,但同时进行的 BFR 会引起严重缺氧,使 PmvO 降低到低于最大(100 Hz)收缩时的水平。低强度电刺激(EXER)可引起肌肉肥大(6.2%,P<0.01),而对照组或单独的 BFR 则没有。EXER+BFR 还引起肌肉质量增加(11.0%,P<0.01),并且在研究的所有条件中,胫骨前肌的表面纤维横截面积显著增加(P<0.05)。EXER+BFR 还增强了核糖体蛋白 S6 的磷酸化,以及过氧化物酶体增殖物激活受体γ共激活因子 1α和葡萄糖转运蛋白 4 的蛋白水平。纤维连接蛋白 III 结构域包含蛋白 5、细胞色素 c 氧化酶亚基 4、单羧酸转运蛋白 1(MCT1)和分化簇 147 的表达随着 EXER 而增加。单独的 EXER 可显著增加 MCT1 的表达。这些数据表明,收缩过程中的微血管缺氧对于肥大并不是必需的。然而,BFR 诱导的缺氧可能会增强肌肉肥大反应(如表面纤维横截面积增加所证明),并增加葡萄糖转运和线粒体生物发生,这有助于 BFR 运动训练的多效性效应,最终导致持续运动能力的提高。新的和值得注意的是,我们研究了收缩过程中低微血管 O 分压(PmvO)对肌肉肥大信号和增加运动能力的肌肉适应关键因素的影响。尽管证明肌肉缺氧不是低强度、电诱导的肌肉收缩引起的肥大反应的必需条件,但降低的 PmvO 增强了核糖体蛋白 S6 的磷酸化,并增强了肥大反应。此外,血流限制引起的收缩增加了氧化能力、葡萄糖转运和线粒体生物发生,这是运动训练多效性效应的关键决定因素。

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