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耐力训练后循环微小RNA谱的改变:一项超马拉松运动员队列研究

Altered Circulating MicroRNA Profiles After Endurance Training: A Cohort Study of Ultramarathon Runners.

作者信息

Eyileten Ceren, Wicik Zofia, Fitas Alex, Marszalek Mikolaj, Simon Jenny E, De Rosa Salvatore, Wiecha Szczepan, Palatini Jeffrey, Postula Marek, Malek Lukasz A

机构信息

Department of Experimental and Clinical Pharmacology, Centre for Preclinical Research and Technology, Medical University of Warsaw, Warsaw, Poland.

Genomics Core Facility, Centre of New Technologies, University of Warsaw, Warsaw, Poland.

出版信息

Front Physiol. 2022 Jan 25;12:792931. doi: 10.3389/fphys.2021.792931. eCollection 2021.

Abstract

BACKGROUND

Despite the positive effects of endurance training on the cardiovascular (CV) system, excessive exercise induces not only physiological adaptations but also adverse changes in CV system, including the heart. We aimed to evaluate the selected miRNAs expression based on bioinformatic analysis and their changes before and after an ultramarathon run.

MATERIALS AND METHODS

Cardiac tissue-specific targets were identified with the Tissue 2.0 database. Gene-gene interaction data were retrieved from the STRING app for Cytoscape. Twenty-three endurance athletes were recruited to the study. Athletes ran to completion (100 km) or exhaustion (52-91 km, median 74 km). All participants completed pre- and post-run testing. miRNAs expressions were measured both before and after the race.

RESULTS

Enrichment analysis of the signaling pathways associated with the genes targeted by miRNAs selected for qRT-PCR validation (miR-1-3p, miR-126, miR-223, miR-125a-5p, miR-106a-5p, and miR-15a/b). All selected miRNAs showed overlap in regulation in pathways associated with cancer, IL-2 signaling, TGF-β signaling as well as BDNF signaling pathway. Analysis of metabolites revealed significant regulation of magnesium and guanosine triphosphate across analyzed miRNA targets. MiR-1-3p, miR-125a-5p, miR-126, and miR-223 expressions were measured in 23 experienced endurance athletes, before and after an ultramarathon wherein athletes ran to completion (100 km) or exhaustion (52-91 km, median 74 km). The expressions of miR-125a-5p, miR-126, and miR-223 were significantly increased after the race ( = 0.007, = 0.001, = 0.014, respectively). MiR-1-3p expression post-run showed a negative correlation with the post-run levels of high-sensitivity C-reactive protein (hs-CRP) ( = -0.632, = 0.003). Higher miR-1-3p expression was found in runners, who finished the race under 10 h compared to runners who finished over 10 h ( = 0.001). Post-run miR-125a-5p expression showed a negative correlation with the peak lactate during the run ( = -0.576, = 0.019).

CONCLUSION

Extreme physical activity, as exemplified by an ultramarathon, is associated with changes in circulating miRNAs' expression related to inflammation, fibrosis, and cardiac muscle function. In particular, the negative correlations between miR-125a-5p and lactate concentrations, and miR-1-3p and hs-CRP, support their role in specific exercise-induced adaptation. Further studies are essential to validate the long-term effect of these observations.

摘要

背景

尽管耐力训练对心血管(CV)系统有积极影响,但过度运动不仅会引起生理适应性变化,还会导致CV系统(包括心脏)出现不良改变。我们旨在基于生物信息学分析评估所选miRNA的表达及其在超级马拉松前后的变化。

材料与方法

使用Tissue 2.0数据库鉴定心脏组织特异性靶点。从用于Cytoscape的STRING应用程序中检索基因-基因相互作用数据。招募了23名耐力运动员参与该研究。运动员跑完全程(100公里)或直至疲惫(52 - 91公里,中位数74公里)。所有参与者在跑步前后均完成测试。在比赛前后均测量miRNA的表达。

结果

对与选择用于qRT-PCR验证的miRNA(miR-1-3p、miR-126、miR-223、miR-125a-5p、miR-106a-5p和miR-15a/b)靶向的基因相关的信号通路进行富集分析。所有选定的miRNA在与癌症、IL-2信号传导、TGF-β信号传导以及BDNF信号通路相关的途径调控中显示出重叠。代谢物分析显示,在所分析的miRNA靶点中,镁和三磷酸鸟苷有显著调控。在23名经验丰富的耐力运动员中测量了miR-1-3p、miR-125a-5p、miR-126和miR-223在超级马拉松前后的表达,其中运动员跑完全程(100公里)或直至疲惫(52 - 91公里,中位数74公里)。赛后miR-125a-5p、miR-126和miR-223的表达显著增加(分别为P = 0.007、P = 0.001、P = 0.014)。赛后miR-1-3p的表达与高敏C反应蛋白(hs-CRP)的赛后水平呈负相关(r = -0.632,P = 0.003)。与用时超过10小时完成比赛的跑步者相比,用时不到10小时完成比赛的跑步者中miR-1-3p表达更高(P = 0.001)。赛后miR-125a-5p的表达与跑步过程中的峰值乳酸呈负相关(r = -0.576,P = 0.019)。

结论

以超级马拉松为例的极限体力活动与循环miRNA表达的变化有关,这些变化与炎症、纤维化和心肌功能相关。特别是,miR-125a-5p与乳酸浓度以及miR-1-3p与hs-CRP之间的负相关支持了它们在特定运动诱导的适应性中的作用。进一步的研究对于验证这些观察结果的长期影响至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2517/8824535/ad1e6fe0b2c8/fphys-12-792931-g001.jpg

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