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Muscle protein synthesis in response to nutrition and exercise

期刊

JOURNAL OF PHYSIOLOGY-LONDON
卷 590, 期 5, 页码 1049-1057

出版社

WILEY
DOI: 10.1113/jphysiol.2011.225003

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资金

  1. Medical Research Council [MR/K00414X/1] Funding Source: Medline
  2. Medical Research Council [MR/K00414X/1] Funding Source: researchfish
  3. MRC [MR/K00414X/1] Funding Source: UKRI

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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 x 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 2040% but maximal at 7090% of one-repetition maximum when workload is matched (according to load x 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 mechanosensingsignalling to MPS.

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