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Lifelong endurance training attenuates age-related genotoxic stress in human skeletal muscle

BACKGROUND: The aim of the present study was to determine the influence of age and habitual activity level, at rest and following a single bout of high-intensity exercise, on the levels of three proteins poly(ADP-ribose) polymerase-1 (PARP-1), cleaved-PARP-1 and poly(ADP-ribose) glycohydrolase (PARG...

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Autores principales: Cobley, James N, Sakellariou, George K, Murray, Scott, Waldron, Sarah, Gregson, Warren, Burniston, Jatin G, Morton, James P, Iwanejko, Lesley A, Close, Graeme L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922955/
https://www.ncbi.nlm.nih.gov/pubmed/24472304
http://dx.doi.org/10.1186/2046-2395-2-11
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author Cobley, James N
Sakellariou, George K
Murray, Scott
Waldron, Sarah
Gregson, Warren
Burniston, Jatin G
Morton, James P
Iwanejko, Lesley A
Close, Graeme L
author_facet Cobley, James N
Sakellariou, George K
Murray, Scott
Waldron, Sarah
Gregson, Warren
Burniston, Jatin G
Morton, James P
Iwanejko, Lesley A
Close, Graeme L
author_sort Cobley, James N
collection PubMed
description BACKGROUND: The aim of the present study was to determine the influence of age and habitual activity level, at rest and following a single bout of high-intensity exercise, on the levels of three proteins poly(ADP-ribose) polymerase-1 (PARP-1), cleaved-PARP-1 and poly(ADP-ribose) glycohydrolase (PARG), involved in the DNA repair and cell death responses to stress and genotoxic insults. Muscle biopsies were obtained from the vastus lateralis of young trained (22 ± 3 years, n = 6), young untrained (24 ± 4 years, n = 6), old trained (64 ± 3 years, n = 6) and old untrained (65 ± 6 years, n = 6) healthy males before, immediately after and three days following a high-intensity interval exercise bout. RESULTS: PARP-1, which catalyzes poly(ADP-ribosyl)ation of proteins and DNA in response to a range of intrinsic and extrinsic stresses, was increased at baseline in old trained and old untrained compared with young trained and young untrained participants (P ≤ 0.05). Following exercise, PARP-1 levels remained unchanged in young trained participants, in contrast to old trained and old untrained where levels decreased and young untrained where levels increased (P ≤ 0.05). Interestingly, baseline levels of the cleaved PARP-1, a marker of apoptosis, and PARG, responsible for polymer degradation, were both significantly elevated in old untrained compared with old trained, young trained and young untrained (P ≤ 0.05). Despite this baseline difference in PARG, there was no change in any group following exercise. There was a non-significant statistical trend (P = 0.072) towards increased cleaved-PARP-1 expression post-exercise in younger but not old persons, regardless of training status. CONCLUSIONS: Collectively, these results show that exercise slows the progression towards a chronically stressed state but has no impact on the age-related attenuated response to acute exercise. Our findings provide valuable insight into how habitual exercise training could protect skeletal muscle from chronic damage to macromolecules and may reduce sarcopenia in older people.
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spelling pubmed-39229552014-02-14 Lifelong endurance training attenuates age-related genotoxic stress in human skeletal muscle Cobley, James N Sakellariou, George K Murray, Scott Waldron, Sarah Gregson, Warren Burniston, Jatin G Morton, James P Iwanejko, Lesley A Close, Graeme L Longev Healthspan Research BACKGROUND: The aim of the present study was to determine the influence of age and habitual activity level, at rest and following a single bout of high-intensity exercise, on the levels of three proteins poly(ADP-ribose) polymerase-1 (PARP-1), cleaved-PARP-1 and poly(ADP-ribose) glycohydrolase (PARG), involved in the DNA repair and cell death responses to stress and genotoxic insults. Muscle biopsies were obtained from the vastus lateralis of young trained (22 ± 3 years, n = 6), young untrained (24 ± 4 years, n = 6), old trained (64 ± 3 years, n = 6) and old untrained (65 ± 6 years, n = 6) healthy males before, immediately after and three days following a high-intensity interval exercise bout. RESULTS: PARP-1, which catalyzes poly(ADP-ribosyl)ation of proteins and DNA in response to a range of intrinsic and extrinsic stresses, was increased at baseline in old trained and old untrained compared with young trained and young untrained participants (P ≤ 0.05). Following exercise, PARP-1 levels remained unchanged in young trained participants, in contrast to old trained and old untrained where levels decreased and young untrained where levels increased (P ≤ 0.05). Interestingly, baseline levels of the cleaved PARP-1, a marker of apoptosis, and PARG, responsible for polymer degradation, were both significantly elevated in old untrained compared with old trained, young trained and young untrained (P ≤ 0.05). Despite this baseline difference in PARG, there was no change in any group following exercise. There was a non-significant statistical trend (P = 0.072) towards increased cleaved-PARP-1 expression post-exercise in younger but not old persons, regardless of training status. CONCLUSIONS: Collectively, these results show that exercise slows the progression towards a chronically stressed state but has no impact on the age-related attenuated response to acute exercise. Our findings provide valuable insight into how habitual exercise training could protect skeletal muscle from chronic damage to macromolecules and may reduce sarcopenia in older people. BioMed Central 2013-07-12 /pmc/articles/PMC3922955/ /pubmed/24472304 http://dx.doi.org/10.1186/2046-2395-2-11 Text en Copyright © 2013 Cobley et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Cobley, James N
Sakellariou, George K
Murray, Scott
Waldron, Sarah
Gregson, Warren
Burniston, Jatin G
Morton, James P
Iwanejko, Lesley A
Close, Graeme L
Lifelong endurance training attenuates age-related genotoxic stress in human skeletal muscle
title Lifelong endurance training attenuates age-related genotoxic stress in human skeletal muscle
title_full Lifelong endurance training attenuates age-related genotoxic stress in human skeletal muscle
title_fullStr Lifelong endurance training attenuates age-related genotoxic stress in human skeletal muscle
title_full_unstemmed Lifelong endurance training attenuates age-related genotoxic stress in human skeletal muscle
title_short Lifelong endurance training attenuates age-related genotoxic stress in human skeletal muscle
title_sort lifelong endurance training attenuates age-related genotoxic stress in human skeletal muscle
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922955/
https://www.ncbi.nlm.nih.gov/pubmed/24472304
http://dx.doi.org/10.1186/2046-2395-2-11
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