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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
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.
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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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