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Long-Term Calorie Restriction Enhances Cellular Quality-Control Processes in Human Skeletal Muscle
Journal article   Open access   Peer reviewed

Long-Term Calorie Restriction Enhances Cellular Quality-Control Processes in Human Skeletal Muscle

Ling Yang, Danilo Licastro, Edda Cava, Nicola Veronese, Francesco Spelta, Wanda Rizza, Beatrice Bertozzi, Dennis T Villareal, Gökhan S Hotamisligil, John O Holloszy, …
Cell reports (Cambridge), Vol.14(3), pp.422-428
01/26/2016
DOI: 10.1016/j.celrep.2015.12.042
PMID: 26774472
url
https://doi.org/10.1016/j.celrep.2015.12.042View
Published (Version of record) Open Access

Abstract

Calorie restriction (CR) retards aging, acts as a hormetic intervention, and increases serum corticosterone and HSP70 expression in rodents. However, less is known regarding the effects of CR on these factors in humans. Serum cortisol and molecular chaperones and autophagic proteins were measured in the skeletal muscle of subjects on CR diets for 3–15 years and in control volunteers. Serum cortisol was higher in the CR group than in age-matched sedentary and endurance athlete groups (15.6 ± 4.6 ng/dl versus 12.3 ± 3.9 ng/dl and 11.2 ± 2.7 ng/dl, respectively; p ≤ 0.001). HSP70, Grp78, beclin-1, and LC3 mRNA and/or protein levels were higher in the skeletal muscle of the CR group compared to controls. Our data indicate that CR in humans is associated with sustained rises in serum cortisol, reduced inflammation, and increases in key molecular chaperones and autophagic mediators involved in cellular protein quality control and removal of dysfunctional proteins and organelles. [Display omitted] •Calorie restriction increases health-span and lifespan in model organisms•Little is known about the metabolic and molecular effects of CR in humans•CR inhibits inflammation in part by increasing serum cortisol concentration•CR elevates expression of genes and proteins that enhance protein quality control Yang et al. show that calorie restriction without malnutrition in humans inhibits inflammation, at least in part by elevating serum cortisol concentration, and increases chaperone and autophagy genes and proteins involved in protein quality control and organelle homeostasis in the removal of dysfunctional proteins and organelles from cell.
cortisol calorie restriction HSP70 autophagy aldosterone

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