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Osmolality Selectively Offsets the Impact of Hyperthermia on Mouse Skeletal Muscle in vitro
Hyperthermia and dehydration can occur during exercise in hot environments. Nevertheless, whether elevations in extracellular osmolality contributes to the increased skeletal muscle tension, sarcolemmal injury, and oxidative stress reported in warm climates remains unknown. We simulated osmotic and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220237/ https://www.ncbi.nlm.nih.gov/pubmed/30429796 http://dx.doi.org/10.3389/fphys.2018.01496 |
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author | Laitano, Orlando Sheikh, Laila H. Mattingly, Alex J. Murray, Kevin O. Ferreira, Leonardo F. Clanton, Thomas L. |
author_facet | Laitano, Orlando Sheikh, Laila H. Mattingly, Alex J. Murray, Kevin O. Ferreira, Leonardo F. Clanton, Thomas L. |
author_sort | Laitano, Orlando |
collection | PubMed |
description | Hyperthermia and dehydration can occur during exercise in hot environments. Nevertheless, whether elevations in extracellular osmolality contributes to the increased skeletal muscle tension, sarcolemmal injury, and oxidative stress reported in warm climates remains unknown. We simulated osmotic and heat stress, in vitro, in mouse limb muscles with different fiber compositions. Extensor digitorum longus (EDL) and soleus (SOL) were dissected from 36 male C57BL6J and mounted at optimal length in tissue baths containing oxygenated buffer. Muscles were stimulated with non-fatiguing twitches for 30 min. Four experimental conditions were tested: isotonic-normothermia (285 mOsm•kg(-1) and 35°C), hypertonic-normothermia (300 mOsm•kg(-1) and 35°C), isotonic-hyperthermia (285 mOsm•kg(-1) and 41°C), and hypertonic-hyperthermia (300 mOsm•kg(-1) and 41°C). Passive tension was recorded continuously. The integrity of the sarcolemma was determined using a cell-impermeable fluorescent dye and immunoblots were used for detection of protein carbonyls. In EDL muscles, isotonic and hypertonic-hyperthermia increased resting tension (P < 0.001). Whereas isotonic-hyperthermia increased sarcolemmal injury in EDL (P < 0.001), this effect was absent in hypertonic-hyperthermia. Similarly, isotonic-hyperthermia elevated protein carbonyls (P = 0.018), a response not observed with hypertonic-hyperthermia. In SOL muscles, isotonic-hyperthermia also increases resting tension (P < 0.001); however, these effects were eliminated in hypertonic-hyperthermia. Unlike EDL, there were no effects of hyperthermia and/or hyperosmolality on sarcolemmal injury or protein carbonyls. Osmolality selectively modifies skeletal muscle response to hyperthermia in this model. Fast-glycolytic muscle appears particularly vulnerable to isotonic-hyperthermia, resulting in elevated muscle tension, sarcolemmal injury and protein oxidation; whereas slow-oxidative muscle exhibits increased tension but no injury or protein oxidation under the conditions and duration tested. |
format | Online Article Text |
id | pubmed-6220237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62202372018-11-14 Osmolality Selectively Offsets the Impact of Hyperthermia on Mouse Skeletal Muscle in vitro Laitano, Orlando Sheikh, Laila H. Mattingly, Alex J. Murray, Kevin O. Ferreira, Leonardo F. Clanton, Thomas L. Front Physiol Physiology Hyperthermia and dehydration can occur during exercise in hot environments. Nevertheless, whether elevations in extracellular osmolality contributes to the increased skeletal muscle tension, sarcolemmal injury, and oxidative stress reported in warm climates remains unknown. We simulated osmotic and heat stress, in vitro, in mouse limb muscles with different fiber compositions. Extensor digitorum longus (EDL) and soleus (SOL) were dissected from 36 male C57BL6J and mounted at optimal length in tissue baths containing oxygenated buffer. Muscles were stimulated with non-fatiguing twitches for 30 min. Four experimental conditions were tested: isotonic-normothermia (285 mOsm•kg(-1) and 35°C), hypertonic-normothermia (300 mOsm•kg(-1) and 35°C), isotonic-hyperthermia (285 mOsm•kg(-1) and 41°C), and hypertonic-hyperthermia (300 mOsm•kg(-1) and 41°C). Passive tension was recorded continuously. The integrity of the sarcolemma was determined using a cell-impermeable fluorescent dye and immunoblots were used for detection of protein carbonyls. In EDL muscles, isotonic and hypertonic-hyperthermia increased resting tension (P < 0.001). Whereas isotonic-hyperthermia increased sarcolemmal injury in EDL (P < 0.001), this effect was absent in hypertonic-hyperthermia. Similarly, isotonic-hyperthermia elevated protein carbonyls (P = 0.018), a response not observed with hypertonic-hyperthermia. In SOL muscles, isotonic-hyperthermia also increases resting tension (P < 0.001); however, these effects were eliminated in hypertonic-hyperthermia. Unlike EDL, there were no effects of hyperthermia and/or hyperosmolality on sarcolemmal injury or protein carbonyls. Osmolality selectively modifies skeletal muscle response to hyperthermia in this model. Fast-glycolytic muscle appears particularly vulnerable to isotonic-hyperthermia, resulting in elevated muscle tension, sarcolemmal injury and protein oxidation; whereas slow-oxidative muscle exhibits increased tension but no injury or protein oxidation under the conditions and duration tested. Frontiers Media S.A. 2018-10-31 /pmc/articles/PMC6220237/ /pubmed/30429796 http://dx.doi.org/10.3389/fphys.2018.01496 Text en Copyright © 2018 Laitano, Sheikh, Mattingly, Murray, Ferreira and Clanton. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Laitano, Orlando Sheikh, Laila H. Mattingly, Alex J. Murray, Kevin O. Ferreira, Leonardo F. Clanton, Thomas L. Osmolality Selectively Offsets the Impact of Hyperthermia on Mouse Skeletal Muscle in vitro |
title | Osmolality Selectively Offsets the Impact of Hyperthermia on Mouse Skeletal Muscle in vitro |
title_full | Osmolality Selectively Offsets the Impact of Hyperthermia on Mouse Skeletal Muscle in vitro |
title_fullStr | Osmolality Selectively Offsets the Impact of Hyperthermia on Mouse Skeletal Muscle in vitro |
title_full_unstemmed | Osmolality Selectively Offsets the Impact of Hyperthermia on Mouse Skeletal Muscle in vitro |
title_short | Osmolality Selectively Offsets the Impact of Hyperthermia on Mouse Skeletal Muscle in vitro |
title_sort | osmolality selectively offsets the impact of hyperthermia on mouse skeletal muscle in vitro |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220237/ https://www.ncbi.nlm.nih.gov/pubmed/30429796 http://dx.doi.org/10.3389/fphys.2018.01496 |
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