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Altered responses in skeletal muscle protein turnover during aging in anabolic and catabolic periods

Abstract : One of the most important effects of aging is sarcopenia, which is associated with impaired locomotion and general weakness. In addition, there is increased susceptibility to illness in aging, which often results in muscle wasting episodes. In such instances, the mobilization of muscle proteins provides free amino acids that are used for energetic purpose, the synthesis of acute phase proteins, and the immune response. However, since muscle protein mass is already depleted, the ability of the aged organism to recover from stress is impaired. Therefore, elucidating the mechanisms that result in sarcopenia is of obvious importance. Age-related changes in protein synthesise and proteolysis are rather small and our current methodology does not enable one to establish unequivocally whether sarcopenia results from depressed protein synthesis, increased proteolysis or both. By contrast, in anabolic and catabolic periods, a number of dysregulations in muscle protein turnover became clearly apparent. The aim of this review is to provide an overview of such altered responses to nutrients and catabolic treatments, which may ultimately contribute to explain sarcopenia. This includes impaired recovery in catabolic states, impaired anabolic effects of nutrients, in particular leucine, and a lack of regulation of the ubiquitin-proteasome proteolytic system. These alterations are discussed with respect to modifications in the insulin/IGF-1 axis and glucocorticoid related effects.
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https://hal.inrae.fr/hal-02681313
Déposant : Migration Prodinra <>
Soumis le : dimanche 31 mai 2020 - 23:16:33
Dernière modification le : vendredi 5 février 2021 - 03:44:21

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Didier Attaix, Laurent Mosoni, Dominique Dardevet, Lydie Combaret, Philippe Patureau-Mirand, et al.. Altered responses in skeletal muscle protein turnover during aging in anabolic and catabolic periods. International Journal of Biochemistry and Cell Biology, Elsevier, 2005, 37 (10), pp.1962-1973. ⟨10.1016/j.biocel.2005.04.009⟩. ⟨hal-02681313⟩

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