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Aerobic Plus Resistance Exercise in Obese Older Adults Improves Muscle Protein Synthesis and Preserves Myocellular Quality Despite Weight Loss.

Citation
Colleluori, G., et al. “Aerobic Plus Resistance Exercise In Obese Older Adults Improves Muscle Protein Synthesis And Preserves Myocellular Quality Despite Weight Loss.”. Cell Metabolism, pp. 261-273.e6.
Center Washington University in St Louis
Author Georgia Colleluori, Lina Aguirre, Uma Phadnis, Kenneth Fowler, Reina Armamento-Villareal, Zheng Sun, Lorenzo Brunetti, Jun Hyoung Park, Benny Abraham Kaipparettu, Nagireddy Putluri, Vimlin Auetumrongsawat, Kevin Yarasheski, Clifford Qualls, Dennis T Villareal
Keywords aging, calorie restriction, Diet, Exercise, lifestyle intervention, muscle protein synthesis, muscle quality, sarcopenia, weight loss
Abstract

Anabolic resistance and impaired myocellular quality contribute to age-related sarcopenia, which exacerbates with obesity. Diet-induced muscle mass loss is attenuated by resistance or aerobic plus resistance exercise compared to aerobic exercise in obese elderly. We assessed chronic effects of weight loss plus different exercise modalities on muscle protein synthesis response to feeding and myocellular quality. Obese older adults were randomized to a weight-management program plus aerobic, resistance, or combined aerobic and resistance exercise or to control. Participants underwent vastus lateralis biopsies at baseline and 6 months. Muscle protein synthesis rate increased more in resistance and combined than in control. Autophagy mediators' expression decreased more in combined than in aerobic, which experienced a higher increase in inflammation and mitochondrial regulators' expression. In obese elderly, combined aerobic and resistance exercise is superior to either mode independently for improving muscle protein synthesis and myocellular quality, thereby maintaining muscle mass during weight-loss therapy.

Year of Publication
2019
Journal
Cell metabolism
Volume
30
Issue
2
Number of Pages
261-273.e6
Date Published
12/2019
ISSN Number
1932-7420
DOI
10.1016/j.cmet.2019.06.008
Alternate Journal
Cell Metab.
PMID
31279675
PMCID
PMC6685749
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