Hubal Monica J, Chen Trevor C, Thompson Paul D, Clarkson Priscilla M
Department of Kinesiology, University of Massachusetts, Amherst, MA, USA.
Am J Physiol Regul Integr Comp Physiol. 2008 May;294(5):R1628-37. doi: 10.1152/ajpregu.00853.2007. Epub 2008 Mar 19.
This study proposed that attenuated expression of inflammatory factors is an underlying mechanism driving the repeated-bout effect (rapid adaptation to eccentric exercise). We investigated changes in mRNA levels and protein localization of inflammatory genes after two bouts of muscle-lengthening exercise. Seven male subjects performed two bouts of lower body exercise (separated by 4 wk) in which one leg performed 300 eccentric-concentric actions, and the contralateral leg performed 300 concentric actions only. Vastus lateralis biopsies were collected at 6 h, and strength was assessed at baseline and at 0, 3, and 5 days after exercise. mRNA levels were measured via semiquantitative RT-PCR for the following genes: CYR61, HSP40, HSP70, IL1R1, TCF8, ZFP36, CEBPD, and MCP1. Muscle functional adaptation was demonstrated via attenuated strength loss (16% less, P = 0.04) at 5 days after bout 2 compared with bout 1 in the eccentrically exercised leg. mRNA expression of three of the eight genes tested was significantly elevated in the eccentrically exercised leg from bout 1 to bout 2 (+3.9-fold for ZFP36, +2.3-fold for CEBPD, and +2.6-fold for MCP1), while all eight mRNA levels were unaffected by bout in the concentrically exercised leg. Immunohistochemistry further localized the protein of one of the elevated factors [monocyte chemoattractant protein-1 (MCP1)] within the tissue. MCP1 colocalized with resident macrophage and satellite cell populations, suggesting that alterations in cytokine signaling between these cell populations may play a role in muscle adaptation to exercise. Contrary to our hypothesis, several inflammatory genes were transcriptionally upregulated (rather than attenuated) after a repeated exercise bout, potentially indicating a role for these genes in the adaptation process.
本研究提出,炎症因子表达减弱是驱动重复运动效应(对离心运动的快速适应)的潜在机制。我们研究了两轮肌肉拉伸运动后炎症基因的mRNA水平和蛋白质定位变化。七名男性受试者进行了两轮下肢运动(间隔4周),其中一条腿进行300次离心 - 向心动作,对侧腿仅进行300次向心动作。在6小时时采集股外侧肌活检样本,并在基线以及运动后0、3和5天评估力量。通过半定量RT-PCR测量以下基因的mRNA水平:CYR61、HSP40、HSP70、IL1R1、TCF8、ZFP36、CEBPD和MCP1。与第一轮相比,第二轮运动后5天,离心运动腿的力量损失减弱(减少16%,P = 0.04),证明了肌肉功能适应。在离心运动腿中,从第一轮运动到第二轮运动,所测试的八个基因中的三个基因的mRNA表达显著升高(ZFP36升高3.9倍,CEBPD升高2.3倍,MCP1升高2.6倍),而在向心运动腿中,所有八个mRNA水平均不受运动轮次的影响。免疫组织化学进一步在组织内定位了其中一种升高因子[单核细胞趋化蛋白-1(MCP1)]的蛋白质。MCP1与驻留巨噬细胞和卫星细胞群体共定位,表明这些细胞群体之间细胞因子信号的改变可能在肌肉对运动的适应中起作用。与我们的假设相反,重复运动一轮后,几个炎症基因在转录水平上上调(而非减弱),这可能表明这些基因在适应过程中发挥作用。