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Multiple sclerosis disease progression: Contributions from a hypoxia–inflammation cycle
Hypoxia has been associated with multiple sclerosis (MS) and is an important area of research. Hypoxia can exacerbate inflammation via the prolylhydroxylase pathway. Inflammation can also trigger hypoxia by damaging mitochondria and endothelial cells to impair blood flow regulation. We hypothesize t...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826859/ https://www.ncbi.nlm.nih.gov/pubmed/30052113 http://dx.doi.org/10.1177/1352458518791683 |
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author | Yang, Runze Dunn, Jeff F |
author_facet | Yang, Runze Dunn, Jeff F |
author_sort | Yang, Runze |
collection | PubMed |
description | Hypoxia has been associated with multiple sclerosis (MS) and is an important area of research. Hypoxia can exacerbate inflammation via the prolylhydroxylase pathway. Inflammation can also trigger hypoxia by damaging mitochondria and endothelial cells to impair blood flow regulation. We hypothesize that there is a “hypoxia–inflammation cycle” in MS which plays an important role in MS disease progression. Therapies that break this cycle may be an interesting area of exploration for treatment of MS. |
format | Online Article Text |
id | pubmed-6826859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-68268592019-12-04 Multiple sclerosis disease progression: Contributions from a hypoxia–inflammation cycle Yang, Runze Dunn, Jeff F Mult Scler Personal Viewpoint Hypoxia has been associated with multiple sclerosis (MS) and is an important area of research. Hypoxia can exacerbate inflammation via the prolylhydroxylase pathway. Inflammation can also trigger hypoxia by damaging mitochondria and endothelial cells to impair blood flow regulation. We hypothesize that there is a “hypoxia–inflammation cycle” in MS which plays an important role in MS disease progression. Therapies that break this cycle may be an interesting area of exploration for treatment of MS. SAGE Publications 2018-07-27 2019-11 /pmc/articles/PMC6826859/ /pubmed/30052113 http://dx.doi.org/10.1177/1352458518791683 Text en © The Author(s), 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Personal Viewpoint Yang, Runze Dunn, Jeff F Multiple sclerosis disease progression: Contributions from a hypoxia–inflammation cycle |
title | Multiple sclerosis disease progression: Contributions from a hypoxia–inflammation cycle |
title_full | Multiple sclerosis disease progression: Contributions from a hypoxia–inflammation cycle |
title_fullStr | Multiple sclerosis disease progression: Contributions from a hypoxia–inflammation cycle |
title_full_unstemmed | Multiple sclerosis disease progression: Contributions from a hypoxia–inflammation cycle |
title_short | Multiple sclerosis disease progression: Contributions from a hypoxia–inflammation cycle |
title_sort | multiple sclerosis disease progression: contributions from a hypoxia–inflammation cycle |
topic | Personal Viewpoint |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826859/ https://www.ncbi.nlm.nih.gov/pubmed/30052113 http://dx.doi.org/10.1177/1352458518791683 |
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