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首页> 外文期刊>BMC Veterinary Research >Evaluation of microRNA expression in plasma and skeletal muscle of thoroughbred racehorses in training
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Evaluation of microRNA expression in plasma and skeletal muscle of thoroughbred racehorses in training

机译:培训纯种赛马血浆和骨骼肌细胞瘤表达的评价

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Circulating 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. Plasma ci-miRNA data for 13/20 horses and all skeletal muscle miRNA data passed quality control. From plasma, 52/179 miRNAs were detected at both time-points. Haemolysis levels were greater than the threshold for accurate quantification of ci-miRNAs in 18/25 resting and all post-exercise plasma samples. Positive correlations (P?
机译:循环miRNA(CI-miRNA)是内源性的,非编码的RNA被出现为潜在的诊断生物标志物。先前已经识别出标准的MIRNA,包括组织特异性miRNA的子集。为了将CI-MiRNA调查为诊断工具,需要识别不同情景的正常表达模式,包括对运动的反应。人类研究表明,随着骨骼肌中表达模式的变化,许多CI-MIRNA是上调的。然而,溶血对准确血浆Ci-miRNA定量的溶解溶解的技术挑战,通常在中等至剧烈运动后天然存在于马匹中。本研究的目的是在良好血统(TB)中锻炼之前和之后的血浆CI-miRNA谱和骨骼肌miRNA,并评估溶解对血浆Ci-miRNA测定的存在和效果。在23个?岁月中评估休息和运动后血浆CI-miRNA谱和溶血分析。休息和运动后骨骼肌miRNA丰度在第二次2?岁的TBS中评估了刚进入Sprint培训。在Sprint训练中从12个TBS静止血液样品中进一步定量溶血。使用含有179mIRNA的人血浆面板用于分析,分光光度分析评估。使用配对的学生的T-Test和Pearson等级相关分析数据。血浆CI-miRNA数据为13/20马和所有骨骼肌miRNA数据通过质量控制。从血浆,在两次点检测52/179 miRNA。溶血水平大于18/25休息和所有锻炼后血浆样品的CI-MIRNA精确定量的阈值。除了4 miRNA的所有除4 miRNA之外,检测到溶血和miRNA丰度之间的正相关(p?<β05),因此不能定量运动诱导的血浆Ci-miRNA表达的变化。在骨骼肌样本中,用5 miRNA(miR-21-5p,let-7d-3p,Let-7d-5p,miR-30b-5p,mir-30e-5p)差异表达(de,时间点之间的p?<?0.05)。在量化高强度运动训练中的马匹中的血浆Ci-miRNA表达之前需要确定溶血度。 De MiRNA在骨骼肌中的鉴定表明miRNA表达的修饰可能有助于TBS中的适应性训练反应。使用人的等离子体面板可能有限地检测了大规模的MIRNA。

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