4.7 Article

Myofibrillar muscle protein synthesis rates subsequent to a meal in response to increasing doses of whey protein at rest and after resistance exercise

期刊

AMERICAN JOURNAL OF CLINICAL NUTRITION
卷 99, 期 1, 页码 86-95

出版社

OXFORD UNIV PRESS
DOI: 10.3945/ajcn.112.055517

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资金

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

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Background: The intake of whey, compared with casein and soy protein intakes, stimulates a greater acute response of muscle protein synthesis (MPS) to protein ingestion in rested and exercised muscle. Objective: We characterized the dose-response relation of postabsorptive rates of myofibrillar MPS to increasing amounts of whey protein at rest and after exercise in resistance-trained, young men. Design: Volunteers (n = 48) consumed a standardized, high-protein (0.54 g/kg body mass) breakfast. Three hours later, a bout of unilateral exercise (8 X 10 leg presses and leg extensions; 80% one-repetition maximum) was performed. Volunteers ingested 0, 10, 20, or 40 g whey protein isolate immediately (similar to 10 min) after exercise. Postabsorptive rates of myofibrillar MPS and whole-body rates of phenylalanine oxidation and urea production were measured over a 4-h postdrink period by continuous tracer infusion of labeled [C-13(6)] phenylalanine and [N-15(2)] urea. Results: Myofibrillar MPS (mean +/- SD) increased (P < 0.05) above 0 g whey protein (0.041 +/- 0.015%/h) by 49% and 56% with the ingestion of 20 and 40 g whey protein, respectively, whereas no additional stimulation was observed with 10 g whey protein (P > 0.05). Rates of phenylalanine oxidation and urea production increased with the ingestion of 40 g whey protein. Conclusions: A 20-g dose of whey protein is sufficient for the maximal stimulation of postabsorptive rates of myofibrillar MPS in rested and exercised muscle of similar to 80-kg resistance-trained, young men. A dose of whey protein >20 g stimulates amino acid oxidation and ureagenesis.

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