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Lifelong exercise, but not short‐term high‐intensity interval training, increases GDF11, a marker of successful aging: a preliminary investigation
Lifelong exercise is associated with regulation of skeletal mass and function, reductions in frailty, and successful aging. Yet, the influence of exercise on myostatin and myostatin‐interacting factors is relatively under examined in older males. Therefore, we investigated whether serum total myosta...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5506528/ https://www.ncbi.nlm.nih.gov/pubmed/28701523 http://dx.doi.org/10.14814/phy2.13343 |
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author | Elliott, Bradley T. Herbert, Peter Sculthorpe, Nicholas Grace, Fergal M. Stratton, Daniel Hayes, Lawrence D. |
author_facet | Elliott, Bradley T. Herbert, Peter Sculthorpe, Nicholas Grace, Fergal M. Stratton, Daniel Hayes, Lawrence D. |
author_sort | Elliott, Bradley T. |
collection | PubMed |
description | Lifelong exercise is associated with regulation of skeletal mass and function, reductions in frailty, and successful aging. Yet, the influence of exercise on myostatin and myostatin‐interacting factors is relatively under examined in older males. Therefore, we investigated whether serum total myostatin, free myostatin, follistatin, and growth and differentiation factor 11 (GDF11) were altered following high‐intensity interval training (HIIT) in a group of 13 lifelong sedentary (SED; 64 [6] years) and 11 lifelong exercising (LEX; 62 [6] years) older males. SED follistatin was moderately greater than LEX pre‐HIIT (Cohen's d = 0.66), and was largely greater post‐HIIT (Cohen's d = 1.22). The HIIT‐induced increase in follistatin was large in SED (Cohen's d = 0.82) and absent in LEX (Cohen's d = 0.03). GDF11 was higher in LEX pre‐HIIT (Cohen's d = 0.49) and post‐HIIT (Cohen's d = 0.63) compared to SED. HIIT resulted in no change to GDF11 in LEX or SED (Cohen's d = 0.00–0.03). Peak power output and GDF11 were correlated (r = 0.603), independent of grouping. Differences in GDF11 with lifelong exercise training, paired with the correlation between GDF11 and peak power output, suggested that GDF11 may be a relevant myostatin‐interacting peptide to successful aging in humans, and strategies to maintain this need to be further explored. |
format | Online Article Text |
id | pubmed-5506528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55065282017-07-13 Lifelong exercise, but not short‐term high‐intensity interval training, increases GDF11, a marker of successful aging: a preliminary investigation Elliott, Bradley T. Herbert, Peter Sculthorpe, Nicholas Grace, Fergal M. Stratton, Daniel Hayes, Lawrence D. Physiol Rep Original Research Lifelong exercise is associated with regulation of skeletal mass and function, reductions in frailty, and successful aging. Yet, the influence of exercise on myostatin and myostatin‐interacting factors is relatively under examined in older males. Therefore, we investigated whether serum total myostatin, free myostatin, follistatin, and growth and differentiation factor 11 (GDF11) were altered following high‐intensity interval training (HIIT) in a group of 13 lifelong sedentary (SED; 64 [6] years) and 11 lifelong exercising (LEX; 62 [6] years) older males. SED follistatin was moderately greater than LEX pre‐HIIT (Cohen's d = 0.66), and was largely greater post‐HIIT (Cohen's d = 1.22). The HIIT‐induced increase in follistatin was large in SED (Cohen's d = 0.82) and absent in LEX (Cohen's d = 0.03). GDF11 was higher in LEX pre‐HIIT (Cohen's d = 0.49) and post‐HIIT (Cohen's d = 0.63) compared to SED. HIIT resulted in no change to GDF11 in LEX or SED (Cohen's d = 0.00–0.03). Peak power output and GDF11 were correlated (r = 0.603), independent of grouping. Differences in GDF11 with lifelong exercise training, paired with the correlation between GDF11 and peak power output, suggested that GDF11 may be a relevant myostatin‐interacting peptide to successful aging in humans, and strategies to maintain this need to be further explored. John Wiley and Sons Inc. 2017-07-12 /pmc/articles/PMC5506528/ /pubmed/28701523 http://dx.doi.org/10.14814/phy2.13343 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Elliott, Bradley T. Herbert, Peter Sculthorpe, Nicholas Grace, Fergal M. Stratton, Daniel Hayes, Lawrence D. Lifelong exercise, but not short‐term high‐intensity interval training, increases GDF11, a marker of successful aging: a preliminary investigation |
title | Lifelong exercise, but not short‐term high‐intensity interval training, increases GDF11, a marker of successful aging: a preliminary investigation |
title_full | Lifelong exercise, but not short‐term high‐intensity interval training, increases GDF11, a marker of successful aging: a preliminary investigation |
title_fullStr | Lifelong exercise, but not short‐term high‐intensity interval training, increases GDF11, a marker of successful aging: a preliminary investigation |
title_full_unstemmed | Lifelong exercise, but not short‐term high‐intensity interval training, increases GDF11, a marker of successful aging: a preliminary investigation |
title_short | Lifelong exercise, but not short‐term high‐intensity interval training, increases GDF11, a marker of successful aging: a preliminary investigation |
title_sort | lifelong exercise, but not short‐term high‐intensity interval training, increases gdf11, a marker of successful aging: a preliminary investigation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5506528/ https://www.ncbi.nlm.nih.gov/pubmed/28701523 http://dx.doi.org/10.14814/phy2.13343 |
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