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The pathways by which mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury

Several studies have demonstrated that mild hypothermia exhibits a neuroprotective role and it can inhibit endothelial cell apoptosis following ischemia/reperfusion injury by decreasing caspase-3 expression. It is hypothesized that mild hypothermia exhibits neuroprotective effects on neurons exposed...

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Autores principales: Luo, Chun, Pan, Su-yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357100/
https://www.ncbi.nlm.nih.gov/pubmed/25788937
http://dx.doi.org/10.4103/1673-5374.150725
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author Luo, Chun
Pan, Su-yue
author_facet Luo, Chun
Pan, Su-yue
author_sort Luo, Chun
collection PubMed
description Several studies have demonstrated that mild hypothermia exhibits a neuroprotective role and it can inhibit endothelial cell apoptosis following ischemia/reperfusion injury by decreasing caspase-3 expression. It is hypothesized that mild hypothermia exhibits neuroprotective effects on neurons exposed to ischemia/reperfusion condition produced by oxygen-glucose deprivation. Mild hypothermia significantly reduced the number of apoptotic neurons, decreased the expression of pro-apoptotic protein Bax and increased mitochondrial membrane potential, with the peak of anti-apoptotic effect appearing between 6 and 12 hours after the injury. These findings indicate that mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury by protecting the mitochondria and that the effective time window is 6–12 hours after ischemia/reperfusion injury.
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spelling pubmed-43571002015-03-18 The pathways by which mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury Luo, Chun Pan, Su-yue Neural Regen Res Research Article Several studies have demonstrated that mild hypothermia exhibits a neuroprotective role and it can inhibit endothelial cell apoptosis following ischemia/reperfusion injury by decreasing caspase-3 expression. It is hypothesized that mild hypothermia exhibits neuroprotective effects on neurons exposed to ischemia/reperfusion condition produced by oxygen-glucose deprivation. Mild hypothermia significantly reduced the number of apoptotic neurons, decreased the expression of pro-apoptotic protein Bax and increased mitochondrial membrane potential, with the peak of anti-apoptotic effect appearing between 6 and 12 hours after the injury. These findings indicate that mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury by protecting the mitochondria and that the effective time window is 6–12 hours after ischemia/reperfusion injury. Medknow Publications & Media Pvt Ltd 2015-01 /pmc/articles/PMC4357100/ /pubmed/25788937 http://dx.doi.org/10.4103/1673-5374.150725 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Luo, Chun
Pan, Su-yue
The pathways by which mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury
title The pathways by which mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury
title_full The pathways by which mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury
title_fullStr The pathways by which mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury
title_full_unstemmed The pathways by which mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury
title_short The pathways by which mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury
title_sort pathways by which mild hypothermia inhibits neuronal apoptosis following ischemia/reperfusion injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357100/
https://www.ncbi.nlm.nih.gov/pubmed/25788937
http://dx.doi.org/10.4103/1673-5374.150725
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