偏心运动引起的迟发性肌肉酸痛和肌肉损伤和炎症标志物的变化。

IF 3.5 4区 医学 Q2 IMMUNOLOGY
Exercise Immunology Review Pub Date : 2013-01-01
Kazue Kanda, Kaoru Sugama, Harumi Hayashida, Jun Sakuma, Yasuo Kawakami, Shigeki Miura, Hiroshi Yoshioka, Yuichi Mori, Katsuhiko Suzuki
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引用次数: 0

摘要

本研究的目的是确定迟发性肌肉酸痛(DOMS)、肌肉损伤和偏心运动炎症反应之间的关系,并探讨其潜在机制。9名健康男性将右腿放在受力板上进行单腿举犊练习。他们在0.5 Hz的频率下进行了10组40次重复的运动,每次运动的负荷相当于他们体重的一半,每组休息3分钟。采用视觉模拟评分法(VAS)评价迟发性肌肉酸痛。分别于运动前、运动后2、4、24、48、72、96 h采集血样和尿样。血液样本分析白细胞差异计数和中性粒细胞功能(迁移活性和氧化爆发活性)。我们还测定了肌肉损伤的血清标志物,肌红蛋白(Mb),血浆和尿前列腺素E2作为镇痛物质。至于炎症介质,分析血浆和尿液中的细胞因子(白细胞介素(IL)-1 β、IL-1受体拮抗剂、IL-2、IL-4、IL-6、IL-8、IL-10、IL-12p40、IL-12p70、肿瘤坏死因子- α、干扰素- γ、单核细胞趋化蛋白-1、粒细胞集落刺激因子、巨噬细胞集落刺激因子和粒细胞巨噬细胞集落刺激因子)、白细胞活化标志物(钙保护蛋白和髓过氧化物酶)、白细胞活化标志物(钙保护蛋白和髓过氧化物酶)。中性粒细胞趋化因子补体5a。所有受试者在随后的几天报告肌肉酸痛,VAS在运动后72小时达到峰值。运动后72 h血清Mb浓度较运动前显著升高(p < 0.05),与运动后72 h VAS升高相关(r = 0.73, p < 0.05)。运动后4 h,循环中性粒细胞计数和迁移活性显著升高(p < 0.01, p < 0.05),而其他血浆和尿液炎症介质无显著变化。这些结果表明,中性粒细胞可以被动员到循环中,并在离心运动后数小时迁移到肌肉组织。运动诱导的4 h中性粒细胞迁移活性的增加与48 h Mb的增加也呈正相关(r = 0.67, p < 0.05)。这些发现提示运动后中性粒细胞的动员和迁移可能参与了肌肉损伤和炎症过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eccentric exercise-induced delayed-onset muscle soreness and changes in markers of muscle damage and inflammation.

The purpose of this study was to determine the relationships among delayed-onset muscle soreness (DOMS), muscle damage and inflammatory responses to eccentric exercise and investigate the underlying mechanisms. Nine healthy males performed one-leg calf-raise exercise with their right leg on a force plate. They performed 10 sets of 40 repetitions of exercise at 0.5 Hz by the load corresponding to the half of their body weight, with a rest for 3 min between sets. DOMS was evaluated by a visual analogue scale (VAS). Blood and urine samples were collected before and 2, 4, 24, 48, 72 and 96 h post-exercise. Blood samples were analyzed for leucocyte differential counts and neutrophil functions (migratory activity and oxidative burst activity). We also determined a serum marker of muscle damage, myoglobin (Mb), and plasma and urinary prostaglandin E2 as an algesic substance. As for the inflammatory mediators, plasma and urine were analyzed for cytokines (interleukin (IL)-1beta, IL-1 receptor antagonist, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p40, IL-12p70, tumour necrosis factor-alpha, interferon-gamma, monocyte chemotactic protein-1, granulocyte colony-stimulating factor, macrophage colony-stimulating factor, and granulocyte macrophage colony-stimulating factor), leucocyte activation markers (calprotectin and myeloperoxidase), and neutrophil chemotactic factor complement 5a. All subjects reported muscle soreness on subsequent days and VAS peaked at 72 h after exercise. Serum Mb concentration significantly increased (p < 0.05) at 72 h after exercise as compared with the pre-exercise values which was correlated with the increases in VAS at 72 h (r = 0.73, p < 0.05). Circulating neutrophil count and migratory activity increased significantly (p < 0.01, and p < 0.05, respectively) at 4 h after exercise, whereas there were no significant changes in the other plasma and urinary inflammatory mediators. These results suggest that neutrophils can be mobilized into the circulation and migrate to the muscle tissue several hours after the eccentric exercise. There were also positive correlations between the exercise-induced increases in neutrophil migratory activity at 4 h and the increases in Mb at 48 h (r = 0.67, p < 0.05). These findings suggest that neutrophil mobilization and migration after exercise may be involved in the muscle damage and inflammatory processes.

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来源期刊
Exercise Immunology Review
Exercise Immunology Review 医学-免疫学
CiteScore
16.00
自引率
0.00%
发文量
7
期刊介绍: Exercise Immunology Review (EIR) serves as the official publication of the International Society of Exercise and Immunology and the German Society of Sports Medicine and Prevention. It is dedicated to advancing knowledge in all areas of immunology relevant to acute exercise and regular physical activity. EIR publishes review articles and papers containing new, original data along with extensive review-like discussions. Recognizing the diverse disciplines contributing to the understanding of immune function, the journal adopts an interdisciplinary approach, facilitating the dissemination of research findings from fields such as exercise sciences, medicine, immunology, physiology, behavioral science, endocrinology, pharmacology, and psychology.
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