Suppr超能文献

先前服用对乙酰氨基酚会影响人体骨骼肌对抗阻运动的早期适应性细胞反应。

Prior acetaminophen consumption impacts the early adaptive cellular response of human skeletal muscle to resistance exercise.

机构信息

Healthy Lifestyles Research Center, Exercise Science and Health Promotion, School of Nutrition and Health Promotion, Arizona State University , Phoenix, Arizona.

Department of Health and Kinesiology, Purdue University , West Lafayette, Indiana.

出版信息

J Appl Physiol (1985). 2018 Apr 1;124(4):1012-1024. doi: 10.1152/japplphysiol.00922.2017. Epub 2018 Jan 11.

Abstract

Resistance exercise (RE) is a powerful stimulus for skeletal muscle adaptation. Previous data demonstrate that cyclooxygenase (COX)-inhibiting drugs alter the cellular mechanisms regulating the adaptive response of skeletal muscle. The purpose of this study was to determine whether prior consumption of the COX inhibitor acetaminophen (APAP) alters the immediate adaptive cellular response in human skeletal muscle after RE. In a double-blinded, randomized, crossover design, healthy young men ( n = 8, 25 ± 1 yr) performed two trials of unilateral knee extension RE (8 sets, 10 reps, 65% max strength). Subjects ingested either APAP (1,000 mg/6 h) or placebo (PLA) for 24 h before RE (final dose consumed immediately after RE). Muscle biopsies (vastus lateralis) were collected at rest and 1 h and 3 h after exercise. Mammalian target of rapamycin (mTOR) complex 1 signaling was assessed through immunoblot and immunohistochemistry, and mRNA expression of myogenic genes was examined via RT-qPCR. At 1 h p-rpS6 was increased in both groups but to a greater extent in PLA. At 3 h p-S6K1 was elevated only in PLA. Furthermore, localization of mTOR to the lysosome (LAMP2) in myosin heavy chain (MHC) II fibers increased 3 h after exercise only in PLA. mTOR-LAMP2 colocalization in MHC I fibers was greater in PLA vs. APAP 1 h after exercise. Myostatin mRNA expression was reduced 1 h after exercise only in PLA. MYF6 mRNA expression was increased 1 h and 3 h after exercise only in APAP. APAP consumption appears to alter the early adaptive cellular response of skeletal muscle to RE. These findings further highlight the mechanisms through which COX-inhibiting drugs impact the adaptive response of skeletal muscle to exercise. NEW & NOTEWORTHY The extent to which the cellular reaction to acetaminophen impacts the mechanisms regulating the adaptive response of human skeletal muscle to resistance exercise is not well understood. Consumption of acetaminophen before resistance exercise appears to suppress the early response of mTORC1 activity to acute resistance exercise. These data also demonstrate, for the first time, that resistance exercise elicits fiber type-specific changes in the intracellular colocalization of mTOR with the lysosome in human skeletal muscle.

摘要

抗阻运动(RE)是骨骼肌肉适应的有力刺激。先前的数据表明,环氧化酶(COX)抑制剂会改变调节骨骼肌肉适应性反应的细胞机制。本研究的目的是确定 COX 抑制剂对乙酰氨基酚(APAP)的预先消耗是否会改变 RE 后人类骨骼肌的即时适应细胞反应。在一项双盲、随机、交叉设计中,健康的年轻男性(n=8,25±1 岁)进行了两次单侧膝关节伸展 RE(8 组,10 次,最大力量的 65%)。受试者在 RE 前 24 小时内分别服用 APAP(1000mg/6h)或安慰剂(PLA)(最后一次剂量在 RE 后立即服用)。在休息时以及运动后 1 小时和 3 小时采集股外侧肌活检。通过免疫印迹和免疫组织化学评估雷帕霉素(mTOR)复合物 1 信号,通过 RT-qPCR 检测肌生成基因的 mRNA 表达。在 1 小时时,两组的 p-rpS6 均增加,但 PLA 组增加更为明显。在 3 小时时,仅 PLA 组的 p-S6K1 升高。此外,仅在 PLA 中,mTOR 向肌球蛋白重链(MHC)II 纤维中的溶酶体(LAMP2)的定位在运动后 3 小时增加。与运动后 1 小时的 APAP 相比,PLA 中 mTOR-LAMP2 的共定位在 MHC I 纤维中更多。仅在 PLA 中,运动后 1 小时肌抑素 mRNA 表达减少。MYF6 mRNA 表达仅在 APAP 运动后 1 小时和 3 小时增加。APAP 消耗似乎改变了骨骼肌肉对 RE 的早期适应性细胞反应。这些发现进一步强调了 COX 抑制剂影响骨骼肌肉对运动适应的机制。新的和值得注意的是,乙酰氨基酚对细胞反应的影响程度会影响调节人类骨骼肌对抗阻运动适应性反应的机制尚不清楚。在抗阻运动前服用对乙酰氨基酚似乎会抑制急性抗阻运动对 mTORC1 活性的早期反应。这些数据还首次表明,抗阻运动会引起人类骨骼肌中 mTOR 与溶酶体的细胞内共定位的纤维类型特异性变化。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验