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Local cryotherapy minimally impacts the metabolome and transcriptome of human skeletal muscle

Cryotherapy is commonly used in the treatment of skeletal muscle injuries. However, the data to support the use of cryotherapy is inconclusive, and the biochemical etiology of cryotherapy in human skeletal muscle remains largely unknown. We therefore sought to determine how a clinically-relevant dos...

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Autores principales: Sarver, Dylan C., Sugg, Kristoffer B., Disser, Nathaniel P., Enselman, Elizabeth R. Sibilsky, Awan, Tariq M., Mendias, Christopher L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445066/
https://www.ncbi.nlm.nih.gov/pubmed/28546635
http://dx.doi.org/10.1038/s41598-017-02754-5
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author Sarver, Dylan C.
Sugg, Kristoffer B.
Disser, Nathaniel P.
Enselman, Elizabeth R. Sibilsky
Awan, Tariq M.
Mendias, Christopher L.
author_facet Sarver, Dylan C.
Sugg, Kristoffer B.
Disser, Nathaniel P.
Enselman, Elizabeth R. Sibilsky
Awan, Tariq M.
Mendias, Christopher L.
author_sort Sarver, Dylan C.
collection PubMed
description Cryotherapy is commonly used in the treatment of skeletal muscle injuries. However, the data to support the use of cryotherapy is inconclusive, and the biochemical etiology of cryotherapy in human skeletal muscle remains largely unknown. We therefore sought to determine how a clinically-relevant dose of cryotherapy would impact the transcriptome and metabolome of skeletal muscle. Eight healthy male subjects (age 24.7 ± 4.5 years, BMI 22.2 ± 1.6) received a 15 minute bout of local cryotherapy, delivered via ice cup massage over the anterolateral thigh. This resulted in an 85% decrease in skin temperature and a predicted 27% reduction in intramuscular temperature. The contralateral side served as a non-treated control. Two hours after cryotherapy, muscle biopsies were obtained to analyze changes in the transcriptome, metabolome, and activation of p38 MAPK, ERK1/2, Akt, and p70S6K proteins. No changes were detected in the transcriptome between control and cooled muscles. Cryotherapy reduced levels of hexose sugars and hypoxanthine by 1.3%, but no statistically different changes were observed in 60 additional metabolites. Overall, no differences in phosphorylated p38 MAPK, ERK1/2, Akt, and p70S6K were observed. A clinically relevant dose of cryotherapy produced negligible acute biochemical and molecular changes in the skeletal muscle of human subjects.
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spelling pubmed-54450662017-05-26 Local cryotherapy minimally impacts the metabolome and transcriptome of human skeletal muscle Sarver, Dylan C. Sugg, Kristoffer B. Disser, Nathaniel P. Enselman, Elizabeth R. Sibilsky Awan, Tariq M. Mendias, Christopher L. Sci Rep Article Cryotherapy is commonly used in the treatment of skeletal muscle injuries. However, the data to support the use of cryotherapy is inconclusive, and the biochemical etiology of cryotherapy in human skeletal muscle remains largely unknown. We therefore sought to determine how a clinically-relevant dose of cryotherapy would impact the transcriptome and metabolome of skeletal muscle. Eight healthy male subjects (age 24.7 ± 4.5 years, BMI 22.2 ± 1.6) received a 15 minute bout of local cryotherapy, delivered via ice cup massage over the anterolateral thigh. This resulted in an 85% decrease in skin temperature and a predicted 27% reduction in intramuscular temperature. The contralateral side served as a non-treated control. Two hours after cryotherapy, muscle biopsies were obtained to analyze changes in the transcriptome, metabolome, and activation of p38 MAPK, ERK1/2, Akt, and p70S6K proteins. No changes were detected in the transcriptome between control and cooled muscles. Cryotherapy reduced levels of hexose sugars and hypoxanthine by 1.3%, but no statistically different changes were observed in 60 additional metabolites. Overall, no differences in phosphorylated p38 MAPK, ERK1/2, Akt, and p70S6K were observed. A clinically relevant dose of cryotherapy produced negligible acute biochemical and molecular changes in the skeletal muscle of human subjects. Nature Publishing Group UK 2017-05-25 /pmc/articles/PMC5445066/ /pubmed/28546635 http://dx.doi.org/10.1038/s41598-017-02754-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sarver, Dylan C.
Sugg, Kristoffer B.
Disser, Nathaniel P.
Enselman, Elizabeth R. Sibilsky
Awan, Tariq M.
Mendias, Christopher L.
Local cryotherapy minimally impacts the metabolome and transcriptome of human skeletal muscle
title Local cryotherapy minimally impacts the metabolome and transcriptome of human skeletal muscle
title_full Local cryotherapy minimally impacts the metabolome and transcriptome of human skeletal muscle
title_fullStr Local cryotherapy minimally impacts the metabolome and transcriptome of human skeletal muscle
title_full_unstemmed Local cryotherapy minimally impacts the metabolome and transcriptome of human skeletal muscle
title_short Local cryotherapy minimally impacts the metabolome and transcriptome of human skeletal muscle
title_sort local cryotherapy minimally impacts the metabolome and transcriptome of human skeletal muscle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445066/
https://www.ncbi.nlm.nih.gov/pubmed/28546635
http://dx.doi.org/10.1038/s41598-017-02754-5
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