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酸敏感离子通道3(ASIC3)在运动过程中通过肌肉酸觉对延迟性肌肉酸痛(DOMS)发挥保护作用。

ASIC3 plays a protective role in delayed-onset muscle soreness (DOMS) through muscle acid sensation during exercise.

作者信息

Khataei Tahsin, Benson Christopher J

机构信息

Department of Internal Medicine, Roy J and Lucile A. Carver College of Medicine, University of Iowa, Iowa City, IA, United States.

Iowa City VA Healthcare System, Iowa City, IA, United States.

出版信息

Front Pain Res (Lausanne). 2023 Sep 19;4:1215197. doi: 10.3389/fpain.2023.1215197. eCollection 2023.

Abstract

Immediate exercise-induced pain (IEIP) and DOMS are two types of exercise-induced muscle pain and can act as barriers to exercise. The burning sensation of IEIP occurs during and immediately after intensive exercise, whereas the soreness of DOMS occurs later. Acid-sensing ion channels (ASICs) within muscle afferents are activated by H and other chemicals and have been shown to play a role in various chronic muscle pain conditions. Here, we further defined the role of ASICs in IEIP, and also tested if ASIC3 is required for DOMS. After undergoing exhaustive treadmill exercise, exercise-induced muscle pain was assessed in wild-type (WT) and mice at baseline via muscle withdrawal threshold (MWT), immediately, and 24 h after exercise. Locomotor movement, grip strength, and repeat exercise performance were tested at baseline and 24 h after exercise to evaluate DOMS. We found that had similar baseline muscle pain, locomotor activity, grip strength, and exercise performance as WT mice. WT showed diminished MWT immediately after exercise indicating they developed IEIP, but mice did not. At 24 h after baseline exercise, both and WT had similarly lower MWT and grip strength, however, displayed significantly lower locomotor activity and repeat exercise performance at 24 h time points compared to WT. In addition, mice had higher muscle injury as measured by serum lactate dehydrogenase and creatine kinase levels at 24 h after exercise. These results show that ASIC3 is required for IEIP, but not DOMS, and in fact might play a protective role to prevent muscle injury associated with strenuous exercise.

摘要

即刻运动诱发疼痛(IEIP)和延迟性肌肉酸痛(DOMS)是两种运动诱发的肌肉疼痛类型,可成为运动的障碍。IEIP的灼痛在高强度运动期间及运动后即刻出现,而DOMS的酸痛则在之后出现。肌肉传入神经中的酸敏感离子通道(ASICs)被H⁺和其他化学物质激活,并已证明在各种慢性肌肉疼痛状况中起作用。在此,我们进一步明确了ASICs在IEIP中的作用,并测试了DOMS是否需要ASIC3。在进行力竭性跑步机运动后,通过肌肉撤离阈值(MWT)在基线、运动后即刻和24小时评估野生型(WT)和[基因敲除]小鼠运动诱发的肌肉疼痛。在基线和运动后24小时测试运动能力、握力和重复运动表现以评估DOMS。我们发现[基因敲除]小鼠与WT小鼠具有相似的基线肌肉疼痛、运动活动能力、握力和运动表现。WT小鼠运动后即刻MWT降低,表明它们出现了IEIP,但[基因敲除]小鼠没有。在基线运动后24小时,[基因敲除]小鼠和WT小鼠的MWT和握力同样降低,然而,与WT小鼠相比,[基因敲除]小鼠在24小时时间点的运动活动能力和重复运动表现显著更低。此外,运动后24小时,通过血清乳酸脱氢酶和肌酸激酶水平测量,[基因敲除]小鼠的肌肉损伤更高。这些结果表明,ASIC3是IEIP所必需的,但不是DOMS所必需的,实际上可能起到保护作用以防止与剧烈运动相关的肌肉损伤。

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