Journal article
Long-Term Calorie Restriction Enhances Cellular Quality-Control Processes in Human Skeletal Muscle
Cell reports (Cambridge), Vol.14(3), pp.422-428
01/26/2016
DOI: 10.1016/j.celrep.2015.12.042
PMID: 26774472
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.
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•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.
Details
- Title: Subtitle
- Long-Term Calorie Restriction Enhances Cellular Quality-Control Processes in Human Skeletal Muscle
- Creators
- Ling Yang - Department of Genetics and Complex Diseases and Sabri Ülker Center, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USADanilo Licastro - CBM Scrl—Genomics, Area Science Park, Basovizza, 34149 Trieste, ItalyEdda Cava - Division of Geriatrics and Nutritional Sciences and Center for Human Nutrition, Washington University School of Medicine, St. Louis, MO 63110, USANicola Veronese - Division of Geriatrics and Nutritional Sciences and Center for Human Nutrition, Washington University School of Medicine, St. Louis, MO 63110, USAFrancesco Spelta - Division of Geriatrics and Nutritional Sciences and Center for Human Nutrition, Washington University School of Medicine, St. Louis, MO 63110, USAWanda Rizza - Division of Geriatrics and Nutritional Sciences and Center for Human Nutrition, Washington University School of Medicine, St. Louis, MO 63110, USABeatrice Bertozzi - Division of Geriatrics and Nutritional Sciences and Center for Human Nutrition, Washington University School of Medicine, St. Louis, MO 63110, USADennis T Villareal - Division of Geriatrics and Nutritional Sciences and Center for Human Nutrition, Washington University School of Medicine, St. Louis, MO 63110, USAGökhan S Hotamisligil - Department of Genetics and Complex Diseases and Sabri Ülker Center, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USAJohn O Holloszy - Division of Geriatrics and Nutritional Sciences and Center for Human Nutrition, Washington University School of Medicine, St. Louis, MO 63110, USALuigi Fontana - Division of Geriatrics and Nutritional Sciences and Center for Human Nutrition, Washington University School of Medicine, St. Louis, MO 63110, USA
- Resource Type
- Journal article
- Publication Details
- Cell reports (Cambridge), Vol.14(3), pp.422-428
- DOI
- 10.1016/j.celrep.2015.12.042
- PMID
- 26774472
- NLM abbreviation
- Cell Rep
- ISSN
- 2211-1247
- eISSN
- 2211-1247
- Publisher
- Elsevier Inc
- Language
- English
- Date published
- 01/26/2016
- Academic Unit
- Molecular Physiology and Biophysics; Anatomy and Cell Biology
- Record Identifier
- 9984025476302771
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