Camera Donny M, Ong Jun N, Coffey Vernon G, Hawley John A
Mary MacKillop Institute for Health Research, Centre for Exercise and Nutrition, Australian Catholic UniversityMelbourne, VIC, Australia; Exercise and Nutrition Research Group, School of Medical Sciences, Royal Melbourne Institute of TechnologyMelbourne, VIC, Australia.
Mary MacKillop Institute for Health Research, Centre for Exercise and Nutrition, Australian Catholic University Melbourne, VIC, Australia.
Front Physiol. 2016 Mar 7;7:87. doi: 10.3389/fphys.2016.00087. eCollection 2016.
We examined changes in the expression of 13 selected skeletal muscle microRNAs (miRNAs) implicated in exercise adaptation responses following a single bout of concurrent exercise. In a randomized cross-over design, seven healthy males undertook a single trial consisting of resistance exercise (8 × 5 leg extension, 80% 1 Repetition Maximum) followed by cycling (30 min at 70% VO2peak) with either post-exercise protein (PRO: 25 g whey protein) or placebo (PLA) ingestion. Muscle biopsies (vastus lateralis) were obtained at rest and 4 h post-exercise. Detection of miRNA via quantitative Polymerase Chain Reaction (qPCR) revealed post-exercise increases in miR-23a-3p (90%), miR-23b-3p (39%), miR-133b (80%), miR-181-5p (50%), and miR-378-5p (41%) at 4 h post-exercise with PRO that also resulted in higher abundance compared to PLA (P < 0.05). There was a post-exercise decrease in miR-494-3p abundance in PLA only (~88%, P < 0.05). There were no changes in the total abundance of target proteins post-exercise or between conditions. Protein ingestion following concurrent exercise can modulate the expression of miRNAs implicated in exercise adaptations compared to placebo. The selective modulation of miRNAs with target proteins that may prioritize myogenic compared to oxidative/metabolic adaptive responses indicate that miRNAs can play a regulatory role in the molecular machinery enhancing muscle protein synthesis responses with protein ingestion following concurrent exercise.
我们研究了13种选定的骨骼肌微小RNA(miRNA)的表达变化,这些miRNA与单次同时进行运动后的运动适应反应有关。在随机交叉设计中,7名健康男性进行了一次试验,包括阻力运动(8组,每组5次腿部伸展,80%的1次重复最大值),随后进行骑行(约70%最大摄氧量下骑行30分钟),运动后分别摄入蛋白质(PRO:25克乳清蛋白)或安慰剂(PLA)。在休息时和运动后4小时采集股外侧肌活检样本。通过定量聚合酶链反应(qPCR)检测miRNA发现,运动后4小时,摄入PRO组的miR-23a-3p(约90%)、miR-23b-3p(约39%)、miR-133b(约80%)、miR-181-5p(约50%)和miR-378-5p(约41%)表达增加,且与PLA组相比丰度更高(P<0.0�)。仅在PLA组中,运动后miR-494-3p丰度下降(约88%,P<0.05)。运动后或不同条件之间靶蛋白的总丰度没有变化。与安慰剂相比,同时进行运动后摄入蛋白质可以调节与运动适应有关的miRNA的表达。与氧化/代谢适应性反应相比,用可能优先促进肌源性的靶蛋白对miRNA进行选择性调节表明,miRNA可以在增强同时进行运动后蛋白质摄入时肌肉蛋白质合成反应的分子机制中发挥调节作用。