Department of Functional Biology (Physiology), University of Oviedo, Oviedo, Spain.
Health Research Institute of the Principality of Asturias (ISPA), Oviedo, Spain.
Scand J Med Sci Sports. 2020 Oct;30(10):1896-1907. doi: 10.1111/sms.13759. Epub 2020 Jul 23.
The systemic response to exercise is dose-dependent and involves a complex gene expression regulation and cross-talk between tissues. This context ARISES the need for analyzing the influence of exercise dose on the profile of circulating microRNAs (c-miRNAs), as emerging posttranscriptional regulators and intercellular communicators. Thus, we hypothesized that different exercise doses will determine specific c-miRNA signatures that will highlight its potential as exercise dose biomarker. Nine active middle-aged males completed a 10-km race (10K), a half-marathon (HM), and a marathon (M). Blood samples were collected immediately before and after races. Plasma RNA was extracted, and a global screening of 752 microRNAs was analyzed using RT-qPCR. Three different c-miRNA profiles were defined according to the three doses. In 10K, 14 c-miRNAs were found to be differentially expressed between pre- and post-exercise, 13 upregulated and 1 downregulated. Regarding HM, 13 c-miRNAs were found to be differentially modulated, in all the cases upregulated. A total of 28 c-miRNAs were found to be differentially expressed in M, 21 overexpressed and 7 repressed after this race. We had also found 3 common c-miRNAs between 10K and M and 2 common c-miRNAs between 10K and HM. In silico analysis supported a close association between exercise dose c-miRNA profiles and cellular pathways linked to energy metabolism and cell cycle. In conclusion, we have observed that different exercise doses induced specific c-miRNA profiles. So, our results point to c-miRNAs as emerging exercise dose biomarkers and as one of regulatory mechanisms modulating the response to endurance exercise.
运动引起的系统性反应是剂量依赖性的,涉及复杂的基因表达调控和组织间的相互作用。这就需要分析运动剂量对循环 microRNAs(c-miRNAs)谱的影响,因为 c-miRNAs 是新兴的转录后调节因子和细胞间通讯分子。因此,我们假设不同的运动剂量将决定特定的 c-miRNA 特征,这将突出其作为运动剂量生物标志物的潜力。9 名活跃的中年男性完成了 10 公里赛跑(10K)、半程马拉松(HM)和马拉松(M)。在比赛前后立即采集血样。提取血浆 RNA,使用 RT-qPCR 对 752 个 microRNAs 进行了全面筛选。根据三种剂量,定义了三种不同的 c-miRNA 谱。在 10K 中,发现 14 个 c-miRNA 在运动前后存在差异表达,其中 13 个上调,1 个下调。对于 HM,发现 13 个 c-miRNA 被不同程度地调节,所有情况都是上调。在 M 中发现 28 个 c-miRNA 差异表达,其中 21 个在比赛后过度表达,7 个受抑制。我们还发现 10K 和 M 之间有 3 个共同的 c-miRNA,10K 和 HM 之间有 2 个共同的 c-miRNA。计算机分析支持运动剂量 c-miRNA 谱与能量代谢和细胞周期相关的细胞途径之间的密切关联。总之,我们观察到不同的运动剂量诱导了特定的 c-miRNA 谱。因此,我们的结果表明 c-miRNAs 是新兴的运动剂量生物标志物,也是调节对耐力运动反应的调节机制之一。