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PPAR Regulation of Inflammatory Signaling in CNS Diseases

Central nervous system (CNS) is an immune privileged site, nevertheless inflammation associates with many CNS diseases. Peroxisome proliferator-activated receptors (PPARs) are a family of nuclear hormone receptors that regulate immune and inflammatory responses. Specific ligands for PPARα, γ, and δ...

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Detalles Bibliográficos
Autores principales: Bright, John J., Kanakasabai, Saravanan, Chearwae, Wanida, Chakraborty, Sharmistha
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2490815/
https://www.ncbi.nlm.nih.gov/pubmed/18670616
http://dx.doi.org/10.1155/2008/658520
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author Bright, John J.
Kanakasabai, Saravanan
Chearwae, Wanida
Chakraborty, Sharmistha
author_facet Bright, John J.
Kanakasabai, Saravanan
Chearwae, Wanida
Chakraborty, Sharmistha
author_sort Bright, John J.
collection PubMed
description Central nervous system (CNS) is an immune privileged site, nevertheless inflammation associates with many CNS diseases. Peroxisome proliferator-activated receptors (PPARs) are a family of nuclear hormone receptors that regulate immune and inflammatory responses. Specific ligands for PPARα, γ, and δ isoforms have proven effective in the animal models of multiple sclerosis (MS), Alzheimer's disease, Parkinson's disease, and trauma/stroke, suggesting their use in the treatment of neuroinflammatory diseases. The activation of NF-κB and Jak-Stat signaling pathways and secretion of inflammatory cytokines are critical in the pathogenesis of CNS diseases. Interestingly, PPAR agonists mitigate CNS disease by modulating inflammatory signaling network in immune cells. In this manuscript, we review the current knowledge on how PPARs regulate neuroinflammatory signaling networks in CNS diseases.
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spelling pubmed-24908152008-07-31 PPAR Regulation of Inflammatory Signaling in CNS Diseases Bright, John J. Kanakasabai, Saravanan Chearwae, Wanida Chakraborty, Sharmistha PPAR Res Review Article Central nervous system (CNS) is an immune privileged site, nevertheless inflammation associates with many CNS diseases. Peroxisome proliferator-activated receptors (PPARs) are a family of nuclear hormone receptors that regulate immune and inflammatory responses. Specific ligands for PPARα, γ, and δ isoforms have proven effective in the animal models of multiple sclerosis (MS), Alzheimer's disease, Parkinson's disease, and trauma/stroke, suggesting their use in the treatment of neuroinflammatory diseases. The activation of NF-κB and Jak-Stat signaling pathways and secretion of inflammatory cytokines are critical in the pathogenesis of CNS diseases. Interestingly, PPAR agonists mitigate CNS disease by modulating inflammatory signaling network in immune cells. In this manuscript, we review the current knowledge on how PPARs regulate neuroinflammatory signaling networks in CNS diseases. Hindawi Publishing Corporation 2008 2008-07-28 /pmc/articles/PMC2490815/ /pubmed/18670616 http://dx.doi.org/10.1155/2008/658520 Text en Copyright © 2008 John J. Bright 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
Bright, John J.
Kanakasabai, Saravanan
Chearwae, Wanida
Chakraborty, Sharmistha
PPAR Regulation of Inflammatory Signaling in CNS Diseases
title PPAR Regulation of Inflammatory Signaling in CNS Diseases
title_full PPAR Regulation of Inflammatory Signaling in CNS Diseases
title_fullStr PPAR Regulation of Inflammatory Signaling in CNS Diseases
title_full_unstemmed PPAR Regulation of Inflammatory Signaling in CNS Diseases
title_short PPAR Regulation of Inflammatory Signaling in CNS Diseases
title_sort ppar regulation of inflammatory signaling in cns diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2490815/
https://www.ncbi.nlm.nih.gov/pubmed/18670616
http://dx.doi.org/10.1155/2008/658520
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