Aging Is Accompanied by a Blunted Muscle Protein Synthetic Response to Protein Ingestion

Progressive loss of skeletal muscle mass with aging (sarcopenia) forms a global health concern. It has been suggested that an impaired capacity to increase muscle protein synthesis rates in response to protein intake is a key contributor to sarcopenia. We assessed whether differences in post-absorpt...

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Published inPloS one Vol. 10; no. 11; p. e0140903
Main Authors Wall, Benjamin Toby, Gorissen, Stefan H., Pennings, Bart, Koopman, René, Groen, Bart B. L., Verdijk, Lex B., van Loon, Luc J. C.
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 04.11.2015
Public Library of Science (PLoS)
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Summary:Progressive loss of skeletal muscle mass with aging (sarcopenia) forms a global health concern. It has been suggested that an impaired capacity to increase muscle protein synthesis rates in response to protein intake is a key contributor to sarcopenia. We assessed whether differences in post-absorptive and/or post-prandial muscle protein synthesis rates exist between large cohorts of healthy young and older men. We performed a cross-sectional, retrospective study comparing in vivo post-absorptive muscle protein synthesis rates determined with stable isotope methodologies between 34 healthy young (22±1 y) and 72 older (75±1 y) men, and post-prandial muscle protein synthesis rates between 35 healthy young (22±1 y) and 40 older (74±1 y) men. Post-absorptive muscle protein synthesis rates did not differ significantly between the young and older group. Post-prandial muscle protein synthesis rates were 16% lower in the older subjects when compared with the young. Muscle protein synthesis rates were >3 fold more responsive to dietary protein ingestion in the young. Irrespective of age, there was a strong negative correlation between post-absorptive muscle protein synthesis rates and the increase in muscle protein synthesis rate following protein ingestion. Aging is associated with the development of muscle anabolic inflexibility which represents a key physiological mechanism underpinning sarcopenia.
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Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: BTW SHG BP RK BBLG LBV LJCvL. Performed the experiments: BTW SHG BP RK BBLG LBV LJCvL. Analyzed the data: BTW SHG LJCvL. Contributed reagents/materials/analysis tools: BTW SHG BP RK LJCvL. Wrote the paper: BTW SHG BP RK BBLG LBV LJCvL.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0140903