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Interleukin-1 Receptor Blockade in Perinatal Brain Injury
Interleukin-1 (IL-1) is a potent inflammatory cytokine that can be produced by a variety of cell types throughout the body. While IL-1 is a central mediator of inflammation and response to infection, the role of IL-1 signaling in adult and pediatric brain injury is becoming increasingly clear. Altho...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4187538/ https://www.ncbi.nlm.nih.gov/pubmed/25340046 http://dx.doi.org/10.3389/fped.2014.00108 |
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author | Rosenzweig, Jason M. Lei, Jun Burd, Irina |
author_facet | Rosenzweig, Jason M. Lei, Jun Burd, Irina |
author_sort | Rosenzweig, Jason M. |
collection | PubMed |
description | Interleukin-1 (IL-1) is a potent inflammatory cytokine that can be produced by a variety of cell types throughout the body. While IL-1 is a central mediator of inflammation and response to infection, the role of IL-1 signaling in adult and pediatric brain injury is becoming increasingly clear. Although the mechanisms of IL-1 expression are largely understood, the downstream effects and contributions to excitotoxicity and oxidative stress are poorly defined. Here, we present a review of mechanisms of IL-1 signaling with a focus on the role of IL-1 in perinatal brain injury. We highlight research models of perinatal brain injury and the use of interleukin-1 receptor antagonist (IL-1RA) as an agent of therapeutic potential in preventing perinatal brain injury due to exposure to inflammation. |
format | Online Article Text |
id | pubmed-4187538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41875382014-10-22 Interleukin-1 Receptor Blockade in Perinatal Brain Injury Rosenzweig, Jason M. Lei, Jun Burd, Irina Front Pediatr Pediatrics Interleukin-1 (IL-1) is a potent inflammatory cytokine that can be produced by a variety of cell types throughout the body. While IL-1 is a central mediator of inflammation and response to infection, the role of IL-1 signaling in adult and pediatric brain injury is becoming increasingly clear. Although the mechanisms of IL-1 expression are largely understood, the downstream effects and contributions to excitotoxicity and oxidative stress are poorly defined. Here, we present a review of mechanisms of IL-1 signaling with a focus on the role of IL-1 in perinatal brain injury. We highlight research models of perinatal brain injury and the use of interleukin-1 receptor antagonist (IL-1RA) as an agent of therapeutic potential in preventing perinatal brain injury due to exposure to inflammation. Frontiers Media S.A. 2014-10-07 /pmc/articles/PMC4187538/ /pubmed/25340046 http://dx.doi.org/10.3389/fped.2014.00108 Text en Copyright © 2014 Rosenzweig, Lei and Burd. 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) or licensor 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 | Pediatrics Rosenzweig, Jason M. Lei, Jun Burd, Irina Interleukin-1 Receptor Blockade in Perinatal Brain Injury |
title | Interleukin-1 Receptor Blockade in Perinatal Brain Injury |
title_full | Interleukin-1 Receptor Blockade in Perinatal Brain Injury |
title_fullStr | Interleukin-1 Receptor Blockade in Perinatal Brain Injury |
title_full_unstemmed | Interleukin-1 Receptor Blockade in Perinatal Brain Injury |
title_short | Interleukin-1 Receptor Blockade in Perinatal Brain Injury |
title_sort | interleukin-1 receptor blockade in perinatal brain injury |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4187538/ https://www.ncbi.nlm.nih.gov/pubmed/25340046 http://dx.doi.org/10.3389/fped.2014.00108 |
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