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Potentially Common Therapeutic Targets for Multiple Sclerosis and Ischemic Stroke

Ischemic stroke (IS) and multiple sclerosis (MS) are two pathologies of the central nervous system (CNS). At the first look, this appears to be the only similarity between the two diseases, as they seem quite different. Indeed IS has an acute onset compared to MS which develops chronically; IS is co...

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Autores principales: Paternò, Roberto, Chillon, Jean-Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053536/
https://www.ncbi.nlm.nih.gov/pubmed/30057552
http://dx.doi.org/10.3389/fphys.2018.00855
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author Paternò, Roberto
Chillon, Jean-Marc
author_facet Paternò, Roberto
Chillon, Jean-Marc
author_sort Paternò, Roberto
collection PubMed
description Ischemic stroke (IS) and multiple sclerosis (MS) are two pathologies of the central nervous system (CNS). At the first look, this appears to be the only similarity between the two diseases, as they seem quite different. Indeed IS has an acute onset compared to MS which develops chronically; IS is consecutive to blood clot migrating to cerebral blood vessels or decrease in cerebral blood flow following atherosclerosis or decreases in cardiac output, whereas MS is an immune disease associated with neurodegeneration. However, both pathologies share similar pathologic pathways and treatments used in MS have been the object of studies in IS. In this mini-review we will discuss similarities between IS and MS on astrocytes and neuroinflammation hallmarks emphasizing the potential for treatments.
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spelling pubmed-60535362018-07-27 Potentially Common Therapeutic Targets for Multiple Sclerosis and Ischemic Stroke Paternò, Roberto Chillon, Jean-Marc Front Physiol Physiology Ischemic stroke (IS) and multiple sclerosis (MS) are two pathologies of the central nervous system (CNS). At the first look, this appears to be the only similarity between the two diseases, as they seem quite different. Indeed IS has an acute onset compared to MS which develops chronically; IS is consecutive to blood clot migrating to cerebral blood vessels or decrease in cerebral blood flow following atherosclerosis or decreases in cardiac output, whereas MS is an immune disease associated with neurodegeneration. However, both pathologies share similar pathologic pathways and treatments used in MS have been the object of studies in IS. In this mini-review we will discuss similarities between IS and MS on astrocytes and neuroinflammation hallmarks emphasizing the potential for treatments. Frontiers Media S.A. 2018-07-13 /pmc/articles/PMC6053536/ /pubmed/30057552 http://dx.doi.org/10.3389/fphys.2018.00855 Text en Copyright © 2018 Paternò and Chillon. 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
Paternò, Roberto
Chillon, Jean-Marc
Potentially Common Therapeutic Targets for Multiple Sclerosis and Ischemic Stroke
title Potentially Common Therapeutic Targets for Multiple Sclerosis and Ischemic Stroke
title_full Potentially Common Therapeutic Targets for Multiple Sclerosis and Ischemic Stroke
title_fullStr Potentially Common Therapeutic Targets for Multiple Sclerosis and Ischemic Stroke
title_full_unstemmed Potentially Common Therapeutic Targets for Multiple Sclerosis and Ischemic Stroke
title_short Potentially Common Therapeutic Targets for Multiple Sclerosis and Ischemic Stroke
title_sort potentially common therapeutic targets for multiple sclerosis and ischemic stroke
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053536/
https://www.ncbi.nlm.nih.gov/pubmed/30057552
http://dx.doi.org/10.3389/fphys.2018.00855
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