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Inflammatory gene changes associated with the repeated-bout effect

机译:与反复发作效应相关的炎性基因改变

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摘要

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 semiquantita-tive 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 chemoat-tractant 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.
机译:这项研究提出,炎症因子的减弱表达是驱动重复发作效应(快速适应离心运动)的潜在机制。我们调查了两次肌肉延长运动后炎症基因的mRNA水平和蛋白质定位的变化。七名男性受试者进行了两次下半身运动(相隔4周),其中一条腿执行了300次偏心同心动作,而对侧腿部仅执行了300次同心动作。在6 h收集外侧股静脉活检,并在基线以及运动后0、3和5天评估强度。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。与偏心锻炼腿部的回合1相比,回合2后5天的减弱的强度损失(减少了16%,P = 0.04)证明了肌肉的功能适应性。在从回合1到回合2的偏心运动腿中,测试的八个基因中的三个基因的mRNA表达显着升高(ZFP36为+3.9倍,CEBPD为+2.3倍,MCP1为+2.6倍),而所有八个mRNA水平不受同心运动腿部回旋的影响。免疫组织化学进一步将组织中一种升高的因子[单核细胞趋化蛋白-1(MCP1)]的蛋白质定位。 MCP1与常驻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传导的改变可能在肌肉适应运动中发挥作用。与我们的假设相反,在反复运动后,一些炎症基因被转录上调(而不是减弱),这可能表明这些基因在适应过程中发挥了作用。

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