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Skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal
OBJECTIVE: We tested the hypothesis that skeletal muscle of endurance-trained male runners would exhibit elevated autophagy and mitophagy markers, which would be associated with greater metabolic flexibility following a high-fat meal (HFM). METHODS: Muscle biopsies were collected to determine differ...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5699914/ https://www.ncbi.nlm.nih.gov/pubmed/29097020 http://dx.doi.org/10.1016/j.molmet.2017.10.006 |
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author | Tarpey, Michael D. Davy, Kevin P. McMillan, Ryan P. Bowser, Suzanne M. Halliday, Tanya M. Boutagy, Nabil E. Davy, Brenda M. Frisard, Madlyn I. Hulver, Matthew W. |
author_facet | Tarpey, Michael D. Davy, Kevin P. McMillan, Ryan P. Bowser, Suzanne M. Halliday, Tanya M. Boutagy, Nabil E. Davy, Brenda M. Frisard, Madlyn I. Hulver, Matthew W. |
author_sort | Tarpey, Michael D. |
collection | PubMed |
description | OBJECTIVE: We tested the hypothesis that skeletal muscle of endurance-trained male runners would exhibit elevated autophagy and mitophagy markers, which would be associated with greater metabolic flexibility following a high-fat meal (HFM). METHODS: Muscle biopsies were collected to determine differences in autophagy and mitophagy protein markers and metabolic flexibility under fasting conditions and 4 h following a HFM between endurance-trained male runners (n = 10) and sedentary, non-obese controls (n = 9). RESULTS: Maximal oxygen consumption (ml·kg·min(−1)) was approximately 50% higher (p < 0.05) in endurance-trained runners compared with sedentary controls (65.8 ± 2.3 and 43.1 ± 3.4, respectively). Autophagy markers were similar between groups. Mitophagy and mitochondrial dynamics protein markers were significantly higher in skeletal muscle of endurance-trained runners compared with sedentary controls in the fasted state, although unaffected by the HFM. Skeletal muscle metabolic flexibility was similar between groups when fasted (p > 0.05), but increased in response to the HFM in endurance-trained athletes only (p < 0.005). Key mitophagy markers, phospho-Pink1(Thr257) and phospho-Parkin(S65) (r = 0.64, p < 0.005), and phospo-Parkin(Ser65) and phospho-Drp1(Ser616) (r = 0.70, p < 0.05) were correlated only within the endurance-trained group. Autophagy and mitophagy markers were not correlated with metabolic flexibility. CONCLUSION: In summary, mitophagy may be enhanced in endurance-trained runners based on elevated markers of mitophagy and mitochondrial dynamics. The HFM did not alter autophagy or mitophagy in either group. The absence of a relationship between mitophagy markers and metabolic flexibility suggests that mitophagy is not a key determinant of metabolic flexibility in a healthy population, but further investigation is warranted. |
format | Online Article Text |
id | pubmed-5699914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56999142017-12-01 Skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal Tarpey, Michael D. Davy, Kevin P. McMillan, Ryan P. Bowser, Suzanne M. Halliday, Tanya M. Boutagy, Nabil E. Davy, Brenda M. Frisard, Madlyn I. Hulver, Matthew W. Mol Metab Original Article OBJECTIVE: We tested the hypothesis that skeletal muscle of endurance-trained male runners would exhibit elevated autophagy and mitophagy markers, which would be associated with greater metabolic flexibility following a high-fat meal (HFM). METHODS: Muscle biopsies were collected to determine differences in autophagy and mitophagy protein markers and metabolic flexibility under fasting conditions and 4 h following a HFM between endurance-trained male runners (n = 10) and sedentary, non-obese controls (n = 9). RESULTS: Maximal oxygen consumption (ml·kg·min(−1)) was approximately 50% higher (p < 0.05) in endurance-trained runners compared with sedentary controls (65.8 ± 2.3 and 43.1 ± 3.4, respectively). Autophagy markers were similar between groups. Mitophagy and mitochondrial dynamics protein markers were significantly higher in skeletal muscle of endurance-trained runners compared with sedentary controls in the fasted state, although unaffected by the HFM. Skeletal muscle metabolic flexibility was similar between groups when fasted (p > 0.05), but increased in response to the HFM in endurance-trained athletes only (p < 0.005). Key mitophagy markers, phospho-Pink1(Thr257) and phospho-Parkin(S65) (r = 0.64, p < 0.005), and phospo-Parkin(Ser65) and phospho-Drp1(Ser616) (r = 0.70, p < 0.05) were correlated only within the endurance-trained group. Autophagy and mitophagy markers were not correlated with metabolic flexibility. CONCLUSION: In summary, mitophagy may be enhanced in endurance-trained runners based on elevated markers of mitophagy and mitochondrial dynamics. The HFM did not alter autophagy or mitophagy in either group. The absence of a relationship between mitophagy markers and metabolic flexibility suggests that mitophagy is not a key determinant of metabolic flexibility in a healthy population, but further investigation is warranted. Elsevier 2017-10-21 /pmc/articles/PMC5699914/ /pubmed/29097020 http://dx.doi.org/10.1016/j.molmet.2017.10.006 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Article Tarpey, Michael D. Davy, Kevin P. McMillan, Ryan P. Bowser, Suzanne M. Halliday, Tanya M. Boutagy, Nabil E. Davy, Brenda M. Frisard, Madlyn I. Hulver, Matthew W. Skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal |
title | Skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal |
title_full | Skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal |
title_fullStr | Skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal |
title_full_unstemmed | Skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal |
title_short | Skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal |
title_sort | skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5699914/ https://www.ncbi.nlm.nih.gov/pubmed/29097020 http://dx.doi.org/10.1016/j.molmet.2017.10.006 |
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