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Skeletal Muscle myomiR Are Differentially Expressed by Endurance Exercise Mode and Combined Essential Amino Acid and Carbohydrate Supplementation

机译:骨骼肌myomiR通过耐力运动模式以及必需氨基酸和碳水化合物的补充补充而差异表达

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摘要

Skeletal muscle microRNAs (myomiR) expression is modulated by exercise, however, the influence of endurance exercise mode, combined with essential amino acid and carbohydrate (EAA+CHO) supplementation are not well defined. This study determined the effects of weighted versus non-weighted endurance exercise, with or without EAA+CHO ingestion on myomiR expression and their association with muscle protein synthesis (MPS). Twenty five adults performed 90 min of metabolically-matched (2.2 VO2 L·m−1) load carriage (LC; performed on a treadmill wearing a vest equal to 30% of individual body mass) or cycle ergometry (CE) exercise, during which EAA+CHO (10 g EAA and 46 g CHO) or non-nutritive control (CON) drinks were consumed. Expression of myomiR (RT-qPCR) were determined at rest (PRE), immediately post-exercise (POST), and 3 h into recovery (REC). Muscle protein synthesis (2H5-phenylalanine) was measured during exercise and recovery. Relative to PRE, POST, and REC expression of miR-1-3p, miR-206, miR-208a-5, and miR-499 was lower (P < 0.05) for LC compared to CE, regardless of dietary treatment. Independent of exercise mode, miR-1-3p and miR-208a-5p expression were lower (P < 0.05) after ingesting EAA+CHO compared to CON. Expression of miR-206 was highest for CE-CON than any other treatment (exercise-by-drink, P < 0.05). Common targets of differing myomiR were identified as markers within mTORC1 signaling, and miR-206 and miR-499 were inversely associated with MPS rates immediately post-exercise. These findings suggest the alterations in myomiR expression between exercise mode and EAA+CHO intake may in part be due to differing MPS modulation immediately post-exercise.
机译:骨骼肌microRNA(myomiR)的表达受运动调节,但是,耐力运动模式与必需氨基酸和碳水化合物(EAA + CHO)的补充结合的影响尚不清楚。这项研究确定了无论有无EAA + CHO摄入,加权与非加权耐力运动对myomiR表达及其与肌肉蛋白质合成(MPS)的关系。 25名成年人进行了90分钟的代谢匹配(2.2 VO2 L·m -1 )负荷运输(LC;在跑步机上进行,穿戴的马甲等于个体体重的30%)或进行了骑行测功(CE)运动,在此期间消耗了EAA + CHO(10克EAA和46克CHO)或非营养性对照(CON)饮料。静息(PRE),运动后立即(POST)和恢复3小时(REC)确定myomiR(RT-qPCR)的表达。在运动和恢复期间测量肌肉蛋白质合成( 2 H5-苯丙氨酸)。与CE相比,无论饮食如何,相对于CE,miR-1-3p,miR-206,miR-208a-5和miR-499的PRE,POST和REC表达均较低(P <0.05)。与运动方式无关,摄入EAA + CHO后的miR-1-3p和miR-208a-5p的表达低于CON(CON)。 CE-CON的miR-206的表达高于其他任何治疗方法(逐次锻炼,P <0.05)。不同的myomiR的共同靶标被鉴定为mTORC1信号内的标志物,并且运动后立即将miR-206和miR-499与MPS率成反比。这些发现表明,运动模式与EAA + CHO摄入量之间的myomiR表达改变可能部分是由于运动后立即改变了MPS调节。

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