使用缺氧信号通路面板比较耐力运动运动员和非运动志愿者的microRNA表达谱

I. Pronina, P. Postnikov, V. I. Pavlov, Z. G. Ordzhonikidze
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引用次数: 1

摘要

近年来,人们对寻找新的潜在分子生物标志物来评估精英运动训练过程的有效性、过载引起的各种病理和滥用违禁物质的兴趣达到了前所未有的水平。在转录后水平调控细胞代谢、分化、增殖和凋亡过程的microrna是在这方面最有价值的候选者。它们存在于人体的所有生物体液中,在长期储存期间是稳定的,并且对环境条件的变化具有抵抗力。众所周知,miRNA表达谱的变化与身体活动密切相关,也与重组激素、促红细胞生成剂和其他提高运动成绩的物质和方法的使用密切相关,这些物质和方法被世界反兴奋剂机构(WADA)禁止。目的:在本研究中,使用缺氧信号通路面板对耐力运动(竞走)运动员和非运动志愿者的血浆样本进行分析,以确定缺氧候选标志物。材料和方法:采用逆转录法和实时定量聚合酶链反应(RT Q-PCR)检测血浆循环mirna的表达谱。使用CFX Manager Software v3.1程序对获得的数据进行统计处理。结果:确定了三种潜在的microRNA标记物:hsa-miR-210-3p, hsa-miR-320a和hsa-miR-935(在运动员中分别增加了61.6倍,51.8倍和41.0倍)-对训练,负荷的生理反应,这可能与耐力训练期间缺氧的出现有关。结论:我们获得了健康的非运动志愿者和职业运动员在非竞赛期循环mirna表达谱差异的初步数据。在未来,我们计划扩大研究的血浆样本,比较运动员在比赛和非比赛期间循环microrna的表达谱,以及比较有氧和无氧负荷时循环microrna的表达谱。此外,当使用缺氧模拟物来提高运动成绩时,分析循环mirna表达水平的变化也是很有意义的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of microRNA expression profiles of athletes involved in endurance sports and non-athletic volunteers using a hypoxia signaling pathway panel
In recent years, interest in the search for new potential molecular biomarkers to assess the effectiveness of the training process in elite sports, various pathologies caused by overload, and abuse of prohibited substances has reached an unprecedented level. MicroRNAs that regulate the processes of metabolism, differentiation, proliferation, and apoptosis of cells at the post-transcriptional level are the most valuable candidates for use in this regard. They are found in all biological fluids of the human body, are stable during long-term storage and resistant to changes in environmental conditions. It is known that changes in the miRNA expression profile are closely associated with physical activity, as well as with the administration of recombinant hormones, erythropoiesis-stimulating agents, and other substances and methods that improve sports performance, which are prohibited by the World Anti-Doping Agency (WADA).Objective: In this study, plasma samples from athletes involved in endurance sports (race walking) and non-athletic volunteers were analyzed using a hypoxia signaling pathway panel to identify hypoxia candidate markers.Materials and methods: Expression profiles of plasma circulating miRNAs were assessed by reverse transcription followed by real-time quantitative polymerase chain reaction (RT Q-PCR). The obtained data were subjected to statistical processing using the CFX Manager Software v3.1 program.Results: Three potential microRNA markers were identified: hsa-miR-210-3p, hsa-miR-320a and hsa-miR-935 (increased in athletes by 61.6 times, 51.8 and 41.0 times, respectively) — of physiological response to the training, load, which may be associated with the emergence of hypoxia during endurance training.Conclusion: We have obtained preliminary data on differences in the expression profiles of circulating miRNAs in healthy non-athletic volunteers and professional athletes in the out-of-competition period. In the future, it is planned to expand the sample of studied blood plasma samples and compare the expression profiles of circulating microRNAs in athletes in competition and out-of-competition periods, as well as to compare the expression profiles of circulating microRNAs during aerobic and anaerobic loads. In addition, it is of interest to analyze changes in the expression levels of circulating miRNAs when using hypoxia mimetics applied to improve sports performance.
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