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      Enhanced Protein Translation Underlies Improved Metabolic and Physical Adaptations to Different Exercise Training Modes in Young and Old Humans

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          Summary

          The molecular transducers of benefits from different exercise modalities remain incompletely defined. Here we report that 12 weeks of high-intensity aerobic interval (HIIT), resistance (RT), and combined exercise training enhanced insulin sensitivity and lean mass, but only HIIT and combined training improved aerobic capacity and skeletal muscle mitochondrial respiration. HIIT revealed a more robust increase in gene transcripts than other exercise modalities, particularly in older adults, although little overlap with corresponding individual protein abundance was noted. HIIT reversed many age-related differences in the proteome, particularly of mitochondrial proteinsin concert with increased mitochondrial protein synthesis. Both RT and HIIT enhanced proteins involved in translational machinery irrespective of age. Only small changes of methylation of DNA promoter regions were observed. We provide evidence for predominant exercise regulation at the translational level, enhancing translational capacity and proteome abundance to explain phenotypic gains in muscle mitochondrial function and hypertrophy in all ages.

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          Author and article information

          Journal
          101233170
          32527
          Cell Metab
          Cell Metab.
          Cell metabolism
          1550-4131
          1932-7420
          29 March 2017
          07 March 2017
          07 March 2018
          : 25
          : 3
          : 581-592
          Affiliations
          [1 ]Division of Endocrinology, Diabetes and Nutrition, Mayo Clinic, Rochester, MN 55905, USA
          [2 ]Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN 55905, USA
          Author notes
          [* ]Correspondence: nair.sree@ 123456mayo.edu
          [3]

          Lead Contact

          Article
          PMC5423095 PMC5423095 5423095 nihpa854685
          10.1016/j.cmet.2017.02.009
          5423095
          28273480
          05d328f2-46b8-4fa3-ac03-72cebd29e843
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