Cargando…

Sex‐specific mitochondrial dynamics and mitophagy response to muscle damage

Muscle damage imposes stress on mitochondria resulting in mitochondrial fusion, fission, and mitophagy. Testosterone is a regulator of these processes. However, no study has examined the effect of sex‐specific resistance exercise (RE)‐induced hormonal response on mitochondrial dynamics and mitophagy...

Descripción completa

Detalles Bibliográficos
Autores principales: Luk, Hui‐Ying, Jiwan, Nigel C., Appell, Casey R., Levitt, Danielle E., Vingren, Jakob L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131605/
https://www.ncbi.nlm.nih.gov/pubmed/35611770
http://dx.doi.org/10.14814/phy2.15230
_version_ 1784713208260460544
author Luk, Hui‐Ying
Jiwan, Nigel C.
Appell, Casey R.
Levitt, Danielle E.
Vingren, Jakob L.
author_facet Luk, Hui‐Ying
Jiwan, Nigel C.
Appell, Casey R.
Levitt, Danielle E.
Vingren, Jakob L.
author_sort Luk, Hui‐Ying
collection PubMed
description Muscle damage imposes stress on mitochondria resulting in mitochondrial fusion, fission, and mitophagy. Testosterone is a regulator of these processes. However, no study has examined the effect of sex‐specific resistance exercise (RE)‐induced hormonal response on mitochondrial dynamics and mitophagy after muscle damage in untrained men and women. Untrained men and women performed two sessions of 80 unilateral maximal eccentric knee extensions (ECC) followed by upper‐body RE (ECC+RE) aimed to induce hormonal changes and maintain a similar lower body demands between conditions or 20 min seated rest (ECC+REST). Vastus lateralis samples were analyzed for gene and protein expression of OPA1, MFN1, DRP1, PINK1, and Parkin at baseline (BL), 12 and 24 h. Testosterone area under the curve was greater for ECC+RE than ECC+REST in men and was greater in men than women for both conditions. A significant time × sex × condition effect was found for Parkin protein expression. At 12 and 24 h, Parkin was lower for ECC + REST than ECC + RE for men; whereas, Parkin was increased at 24 h for women regardless of condition. A significant time effect was found for OPA1 protein expression increasing at 12 and 24 h. A significant time × sex × condition effects were found for MFN1, DRP1, and PINK1 gene expression with increases at 12 h in men for ECC + RE. A significant time × sex effect was found for OPA1 gene expression with a decrease at 12 h in men, and 12 h expression in men was lower than women. RE‐induced hormonal changes promoted expression of fission, fusion, and mitophagy markers in men. With muscle damage, regardless of condition, expression of inner mitochondrial membrane fusion markers are promoted in both sexes; whereas, those for mitophagy were promoted in women but reduced in men.
format Online
Article
Text
id pubmed-9131605
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-91316052022-05-26 Sex‐specific mitochondrial dynamics and mitophagy response to muscle damage Luk, Hui‐Ying Jiwan, Nigel C. Appell, Casey R. Levitt, Danielle E. Vingren, Jakob L. Physiol Rep Original Articles Muscle damage imposes stress on mitochondria resulting in mitochondrial fusion, fission, and mitophagy. Testosterone is a regulator of these processes. However, no study has examined the effect of sex‐specific resistance exercise (RE)‐induced hormonal response on mitochondrial dynamics and mitophagy after muscle damage in untrained men and women. Untrained men and women performed two sessions of 80 unilateral maximal eccentric knee extensions (ECC) followed by upper‐body RE (ECC+RE) aimed to induce hormonal changes and maintain a similar lower body demands between conditions or 20 min seated rest (ECC+REST). Vastus lateralis samples were analyzed for gene and protein expression of OPA1, MFN1, DRP1, PINK1, and Parkin at baseline (BL), 12 and 24 h. Testosterone area under the curve was greater for ECC+RE than ECC+REST in men and was greater in men than women for both conditions. A significant time × sex × condition effect was found for Parkin protein expression. At 12 and 24 h, Parkin was lower for ECC + REST than ECC + RE for men; whereas, Parkin was increased at 24 h for women regardless of condition. A significant time effect was found for OPA1 protein expression increasing at 12 and 24 h. A significant time × sex × condition effects were found for MFN1, DRP1, and PINK1 gene expression with increases at 12 h in men for ECC + RE. A significant time × sex effect was found for OPA1 gene expression with a decrease at 12 h in men, and 12 h expression in men was lower than women. RE‐induced hormonal changes promoted expression of fission, fusion, and mitophagy markers in men. With muscle damage, regardless of condition, expression of inner mitochondrial membrane fusion markers are promoted in both sexes; whereas, those for mitophagy were promoted in women but reduced in men. John Wiley and Sons Inc. 2022-05-25 /pmc/articles/PMC9131605/ /pubmed/35611770 http://dx.doi.org/10.14814/phy2.15230 Text en © 2022 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Articles
Luk, Hui‐Ying
Jiwan, Nigel C.
Appell, Casey R.
Levitt, Danielle E.
Vingren, Jakob L.
Sex‐specific mitochondrial dynamics and mitophagy response to muscle damage
title Sex‐specific mitochondrial dynamics and mitophagy response to muscle damage
title_full Sex‐specific mitochondrial dynamics and mitophagy response to muscle damage
title_fullStr Sex‐specific mitochondrial dynamics and mitophagy response to muscle damage
title_full_unstemmed Sex‐specific mitochondrial dynamics and mitophagy response to muscle damage
title_short Sex‐specific mitochondrial dynamics and mitophagy response to muscle damage
title_sort sex‐specific mitochondrial dynamics and mitophagy response to muscle damage
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131605/
https://www.ncbi.nlm.nih.gov/pubmed/35611770
http://dx.doi.org/10.14814/phy2.15230
work_keys_str_mv AT lukhuiying sexspecificmitochondrialdynamicsandmitophagyresponsetomuscledamage
AT jiwannigelc sexspecificmitochondrialdynamicsandmitophagyresponsetomuscledamage
AT appellcaseyr sexspecificmitochondrialdynamicsandmitophagyresponsetomuscledamage
AT levittdaniellee sexspecificmitochondrialdynamicsandmitophagyresponsetomuscledamage
AT vingrenjakobl sexspecificmitochondrialdynamicsandmitophagyresponsetomuscledamage