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Evaluation of microRNA expression in plasma and skeletal muscle of thoroughbred racehorses in training

机译:训练中纯种赛马血浆和骨骼肌中microRNA表达的评估

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摘要

BackgroundCirculating miRNAs (ci-miRNAs) are endogenous, non-coding RNAs emerging as potential diagnostic biomarkers. Equine miRNAs have been previously identified including subsets of tissue-specific miRNAs. In order to investigate ci-miRNAs as diagnostic tools, normal patterns of expression for different scenarios including responses to exercise need to be identified. Human studies have demonstrated that many ci-miRNAs are up-regulated following exercise with changes in expression patterns in skeletal muscle. However, technical challenges such as haemolysis impact on accurate plasma ci-miRNA quantification, with haemolysis often occurring naturally in horses following moderate-to-intense exercise. The objectives of this study were to identify plasma ci-miRNA profiles and skeletal muscle miRNAs before and after exercise in Thoroughbreds (Tb), and to evaluate for the presence and effect of haemolysis on plasma ci-miRNA determination. Resting and post-exercise plasma ci-miRNA profiles and haemolysis were evaluated in twenty 3 year-old Tbs in sprint training. Resting and post-exercise skeletal muscle miRNA abundance was evaluated in a second cohort of eleven 2 year-old Tbs just entering sprint training. Haemolysis was further quantified in resting blood samples from twelve Tbs in sprint training. A human plasma panel containing 179 miRNAs was used for profiling, with haemolysis assessed spectrophotometrically. Data was analysed using a paired Student’s t-test and Pearson’s rank correlation.
机译:背景技术循环miRNA(ci-miRNA)是内源性非编码RNAs,正在成为潜在的诊断生物标志物。先前已鉴定出马miRNA,包括组织特异性miRNA的子集。为了研究ci-miRNAs作为诊断工具,需要确定不同情况下的正常表达模式,包括对运动的反应。人体研究表明,运动后许多ci-miRNA均会随着骨骼肌表达模式的变化而上调。但是,诸如溶血作用等技术挑战会影响血浆ci-miRNA的准确定量,溶血作用通常是在中度至剧烈运动后自然发生在马匹中。这项研究的目的是确定纯种(Tb)运动前后的血浆ci-miRNA概况和骨骼肌miRNA,并评估溶血对血浆ci-miRNA测定的存在和影响。在短跑训练中的20个3岁的Tb中评估了休息和运动后血浆ci-miRNA的概况以及溶血情况。在刚刚进入短跑训练的11名2岁Tb的第二个队列中评估了休息和运动后骨骼肌miRNA的丰度。在冲刺训练中,对来自十二个Tb的静息血液样本中的溶血进行了进一步定量。使用包含179个miRNA的人血浆样本进行分析,并通过分光光度法评估溶血作用。使用配对的Student t检验和Pearson的排名相关性对数据进行了分析。

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