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Exercise rapidly alters proteomes in mice following spinal cord demyelination
Exercise affords broad benefits for people with multiple sclerosis (PwMS) including less fatigue, depression, and improved cognition. In animal models of multiple sclerosis (MS), exercise has been shown to improve remyelination, decrease blood–brain barrier permeability and reduce leukocyte infiltra...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012633/ https://www.ncbi.nlm.nih.gov/pubmed/33790323 http://dx.doi.org/10.1038/s41598-021-86593-5 |
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author | Lozinski, Brian Mark de Almeida, Luiz Gustavo Nogueira Silva, Claudia Dong, Yifei Brown, Dennis Chopra, Sameeksha Yong, V. Wee Dufour, Antoine |
author_facet | Lozinski, Brian Mark de Almeida, Luiz Gustavo Nogueira Silva, Claudia Dong, Yifei Brown, Dennis Chopra, Sameeksha Yong, V. Wee Dufour, Antoine |
author_sort | Lozinski, Brian Mark |
collection | PubMed |
description | Exercise affords broad benefits for people with multiple sclerosis (PwMS) including less fatigue, depression, and improved cognition. In animal models of multiple sclerosis (MS), exercise has been shown to improve remyelination, decrease blood–brain barrier permeability and reduce leukocyte infiltration. Despite these benefits many PwMS refrain from engaging in physical activity. This barrier to participation in exercise may be overcome by uncovering and describing the mechanisms by which exercise promotes beneficial changes in the central nervous system (CNS). Here, we show that acute bouts of exercise in mice profoundly alters the proteome in demyelinating lesions. Following lysolecithin induced demyelination of the ventral spinal cord, mice were given immediate access to a running wheel for 4 days. Lesioned spinal cords and peripheral blood serum were then subjected to tandem mass tag labeling shotgun proteomics workflow to identify alteration in protein levels. We identified 86 significantly upregulated and 85 downregulated proteins in the lesioned spinal cord as well as 14 significantly upregulated and 11 downregulated proteins in the serum following acute exercise. Altered pathways following exercise in demyelinated mice include oxidative stress response, metabolism and transmission across chemical synapses. Similar acute bout of exercise in naïve mice also changed several proteins in the serum and spinal cord, including those for metabolism and anti-oxidant responses. Improving our understanding of the mechanisms and duration of activity required to influence the injured CNS should motivate PwMS and other conditions to embrace exercise as part of their therapy to manage CNS disability. |
format | Online Article Text |
id | pubmed-8012633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80126332021-04-05 Exercise rapidly alters proteomes in mice following spinal cord demyelination Lozinski, Brian Mark de Almeida, Luiz Gustavo Nogueira Silva, Claudia Dong, Yifei Brown, Dennis Chopra, Sameeksha Yong, V. Wee Dufour, Antoine Sci Rep Article Exercise affords broad benefits for people with multiple sclerosis (PwMS) including less fatigue, depression, and improved cognition. In animal models of multiple sclerosis (MS), exercise has been shown to improve remyelination, decrease blood–brain barrier permeability and reduce leukocyte infiltration. Despite these benefits many PwMS refrain from engaging in physical activity. This barrier to participation in exercise may be overcome by uncovering and describing the mechanisms by which exercise promotes beneficial changes in the central nervous system (CNS). Here, we show that acute bouts of exercise in mice profoundly alters the proteome in demyelinating lesions. Following lysolecithin induced demyelination of the ventral spinal cord, mice were given immediate access to a running wheel for 4 days. Lesioned spinal cords and peripheral blood serum were then subjected to tandem mass tag labeling shotgun proteomics workflow to identify alteration in protein levels. We identified 86 significantly upregulated and 85 downregulated proteins in the lesioned spinal cord as well as 14 significantly upregulated and 11 downregulated proteins in the serum following acute exercise. Altered pathways following exercise in demyelinated mice include oxidative stress response, metabolism and transmission across chemical synapses. Similar acute bout of exercise in naïve mice also changed several proteins in the serum and spinal cord, including those for metabolism and anti-oxidant responses. Improving our understanding of the mechanisms and duration of activity required to influence the injured CNS should motivate PwMS and other conditions to embrace exercise as part of their therapy to manage CNS disability. Nature Publishing Group UK 2021-03-31 /pmc/articles/PMC8012633/ /pubmed/33790323 http://dx.doi.org/10.1038/s41598-021-86593-5 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lozinski, Brian Mark de Almeida, Luiz Gustavo Nogueira Silva, Claudia Dong, Yifei Brown, Dennis Chopra, Sameeksha Yong, V. Wee Dufour, Antoine Exercise rapidly alters proteomes in mice following spinal cord demyelination |
title | Exercise rapidly alters proteomes in mice following spinal cord demyelination |
title_full | Exercise rapidly alters proteomes in mice following spinal cord demyelination |
title_fullStr | Exercise rapidly alters proteomes in mice following spinal cord demyelination |
title_full_unstemmed | Exercise rapidly alters proteomes in mice following spinal cord demyelination |
title_short | Exercise rapidly alters proteomes in mice following spinal cord demyelination |
title_sort | exercise rapidly alters proteomes in mice following spinal cord demyelination |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012633/ https://www.ncbi.nlm.nih.gov/pubmed/33790323 http://dx.doi.org/10.1038/s41598-021-86593-5 |
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