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Scand J Med Sci Sports. 2013 Jun;23(3):355-66. doi: 10.1111/j.1600-0838.2011.01395.x.
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Recent progress toward understanding the molecular mechanisms that regulate skeletal muscle mass.骨骼肌质量调控的分子机制研究进展。
Cell Signal. 2011 Dec;23(12):1896-906. doi: 10.1016/j.cellsig.2011.07.013. Epub 2011 Jul 23.
3
Aerobic exercise training adaptations are increased by postexercise carbohydrate-protein supplementation.运动后补充碳水化合物-蛋白质可增强有氧运动训练的适应性。
J Nutr Metab. 2011;2011:623182. doi: 10.1155/2011/623182. Epub 2011 Jun 9.
4
Similar increases in muscle size and strength in young men after training with maximal shortening or lengthening contractions when matched for total work.在总工作量相匹配的情况下,年轻人进行最大缩短或延长收缩训练后,肌肉大小和力量的增加相似。
Eur J Appl Physiol. 2012 Apr;112(4):1587-92. doi: 10.1007/s00421-011-2078-x. Epub 2011 Jul 14.
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In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.通过激活 AMPK/PGC-1α 轴纠正 COX 缺陷
Cell Metab. 2011 Jul 6;14(1):80-90. doi: 10.1016/j.cmet.2011.04.011.
6
Mechanotransduction and the regulation of mTORC1 signaling in skeletal muscle.机械转导与 mTORC1 信号在骨骼肌中的调节。
Int J Biochem Cell Biol. 2011 Sep;43(9):1267-76. doi: 10.1016/j.biocel.2011.05.007. Epub 2011 May 19.
7
Long-term synthesis rates of skeletal muscle DNA and protein are higher during aerobic training in older humans than in sedentary young subjects but are not altered by protein supplementation.在老年人进行有氧运动训练时,骨骼肌 DNA 和蛋白质的长期合成率高于久坐的年轻受试者,但蛋白质补充不会改变这一结果。
FASEB J. 2011 Sep;25(9):3240-9. doi: 10.1096/fj.11-186437. Epub 2011 May 25.
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Mammalian target of rapamycin complex 1 activation is required for the stimulation of human skeletal muscle protein synthesis by essential amino acids.哺乳动物雷帕霉素靶蛋白复合物 1 的激活对于必需氨基酸刺激人体骨骼肌蛋白质合成是必需的。
J Nutr. 2011 May;141(5):856-62. doi: 10.3945/jn.111.139485. Epub 2011 Mar 23.
9
mTOR Signalling in Health and Disease.mTOR 信号通路在健康与疾病中的作用
Biochem Soc Trans. 2011 Apr;39(2):431-6. doi: 10.1042/BST0390431.
10
Enhanced amino acid sensitivity of myofibrillar protein synthesis persists for up to 24 h after resistance exercise in young men.在年轻男性进行抗阻运动后,肌原纤维蛋白合成的氨基酸敏感性增强可持续长达 24 小时。
J Nutr. 2011 Apr 1;141(4):568-73. doi: 10.3945/jn.110.135038. Epub 2011 Feb 2.

营养与运动对肌肉蛋白质合成的影响。

Muscle protein synthesis in response to nutrition and exercise.

机构信息

School of Graduate Entry Medicine and Health, Division of Metabolic Physiology, University of Nottingham, Derby Royal Hospital, Uttoxeter Road, Derby DE22 3DT, UK.

出版信息

J Physiol. 2012 Mar 1;590(5):1049-57. doi: 10.1113/jphysiol.2011.225003. Epub 2012 Jan 30.

DOI:10.1113/jphysiol.2011.225003
PMID:22289911
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3381813/
Abstract

Muscle protein synthesis (MPS) is the driving force behind adaptive responses to exercise and represents a widely adopted proxy for gauging chronic efficacy of acute interventions, (i.e. exercise/nutrition). Recent findings in this arena have been progressive. Nutrient-driven increases in MPS are of finite duration (∼1.5 h), switching off thereafter despite sustained amino acid availability and intramuscular anabolic signalling. Intriguingly, this 'muscle-full set-point' is delayed by resistance exercise (RE) (i.e. the feeding × exercise combination is 'more anabolic' than nutrition alone) even 24 h beyond a single exercise bout, casting doubt on the importance of nutrient timing vs. sufficiency per se. Studies manipulating exercise intensity/workload have shown that increases in MPS are negligible with RE at 20-40% but maximal at 70-90% of one-repetition maximum when workload is matched (according to load × repetition number). However, low-intensity exercise performed to failure equalises this response. Analysing distinct subcellular fractions (e.g. myofibrillar, sarcoplasmic, mitochondrial) may provide a readout of chronic exercise efficacy in addition to effect size in MPS per se, i.e. while 'mixed' MPS increases similarly with endurance and RE, increases in myofibrillar MPS are specific to RE, prophetic of adaptation (i.e. hypertrophy). Finally, the molecular regulation of MPS by exercise and its regulation via 'anabolic' hormones (e.g. IGF-1) has been questioned, leading to discovery of alternative mechanosensing-signalling to MPS.

摘要

肌肉蛋白质合成(MPS)是运动适应反应的驱动力,也是衡量急性干预慢性效果的广泛采用的指标(例如运动/营养)。该领域的最新发现进展迅速。尽管氨基酸供应和肌肉内合成代谢信号持续存在,但营养驱动的 MPS 增加持续时间有限(约 1.5 小时),此后就会关闭。有趣的是,抵抗运动(RE)会延迟这种“肌肉完全设定点”(即,进食与运动的组合比单独营养更具合成代谢作用),即使在单次运动后 24 小时也会延迟,这使得营养时机与本身的充足性的重要性受到质疑。研究表明,通过调整运动强度/工作量,当 RE 强度为 20-40%时,MPS 的增加可以忽略不计,但当工作量相匹配(根据负荷×重复次数)时,RE 强度达到 70-90%时 MPS 会最大程度增加。然而,当低强度运动达到疲劳时,这种反应会趋于平衡。分析不同的亚细胞成分(例如肌原纤维、肌浆和线粒体)除了本身的 MPS 效应大小外,还可以提供慢性运动效果的指标,即虽然“混合”MPS 会随着耐力和 RE 而相似增加,但肌原纤维 MPS 的增加是 RE 特有的,预示着适应(即肥大)。最后,运动对 MPS 的分子调节及其通过“合成代谢”激素(例如 IGF-1)的调节受到质疑,导致了对 MPS 的替代机械传感信号的发现。