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Neuroprotective Effects of Lipoxin A4 in Central Nervous System Pathologies

Many diseases of the central nervous system are characterized and sometimes worsened by an intense inflammatory response in the affected tissue. It is now accepted that resolution of inflammation is an active process mediated by a group of mediators that can act in synchrony to switch the phenotype...

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Autores principales: Martini, Alessandra Cadete, Forner, Stefânia, Bento, Allisson Freire, Rae, Giles Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174961/
https://www.ncbi.nlm.nih.gov/pubmed/25276776
http://dx.doi.org/10.1155/2014/316204
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author Martini, Alessandra Cadete
Forner, Stefânia
Bento, Allisson Freire
Rae, Giles Alexander
author_facet Martini, Alessandra Cadete
Forner, Stefânia
Bento, Allisson Freire
Rae, Giles Alexander
author_sort Martini, Alessandra Cadete
collection PubMed
description Many diseases of the central nervous system are characterized and sometimes worsened by an intense inflammatory response in the affected tissue. It is now accepted that resolution of inflammation is an active process mediated by a group of mediators that can act in synchrony to switch the phenotype of cells, from a proinflammatory one to another that favors the return to homeostasis. This new genus of proresolving mediators includes resolvins, protectins, maresins, and lipoxins, the first to be discovered. In this short review we provide an overview of current knowledge into the cellular and molecular interactions of lipoxins in diseases of the central nervous system in which they appear to facilitate the resolution of inflammation, thus exerting a neuroprotective action.
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spelling pubmed-41749612014-09-30 Neuroprotective Effects of Lipoxin A4 in Central Nervous System Pathologies Martini, Alessandra Cadete Forner, Stefânia Bento, Allisson Freire Rae, Giles Alexander Biomed Res Int Review Article Many diseases of the central nervous system are characterized and sometimes worsened by an intense inflammatory response in the affected tissue. It is now accepted that resolution of inflammation is an active process mediated by a group of mediators that can act in synchrony to switch the phenotype of cells, from a proinflammatory one to another that favors the return to homeostasis. This new genus of proresolving mediators includes resolvins, protectins, maresins, and lipoxins, the first to be discovered. In this short review we provide an overview of current knowledge into the cellular and molecular interactions of lipoxins in diseases of the central nervous system in which they appear to facilitate the resolution of inflammation, thus exerting a neuroprotective action. Hindawi Publishing Corporation 2014 2014-09-09 /pmc/articles/PMC4174961/ /pubmed/25276776 http://dx.doi.org/10.1155/2014/316204 Text en Copyright © 2014 Alessandra Cadete Martini et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Martini, Alessandra Cadete
Forner, Stefânia
Bento, Allisson Freire
Rae, Giles Alexander
Neuroprotective Effects of Lipoxin A4 in Central Nervous System Pathologies
title Neuroprotective Effects of Lipoxin A4 in Central Nervous System Pathologies
title_full Neuroprotective Effects of Lipoxin A4 in Central Nervous System Pathologies
title_fullStr Neuroprotective Effects of Lipoxin A4 in Central Nervous System Pathologies
title_full_unstemmed Neuroprotective Effects of Lipoxin A4 in Central Nervous System Pathologies
title_short Neuroprotective Effects of Lipoxin A4 in Central Nervous System Pathologies
title_sort neuroprotective effects of lipoxin a4 in central nervous system pathologies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174961/
https://www.ncbi.nlm.nih.gov/pubmed/25276776
http://dx.doi.org/10.1155/2014/316204
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