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Selective brain hypothermia attenuates focal cerebral ischemic injury and improves long‐term neurological outcome in aged female mice

AIMS: This study aimed to investigate the effects of mild selective brain hypothermia on aged female ischemic mice. METHODS: A distal middle cerebral artery occlusion (dMCAO) model was established in aged female mice, who were then subjected to mild selective brain hypothermia immediately after the...

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Autores principales: Liu, Liqiang, Liu, Jia, Li, Ming, Lyu, Junxuan, Su, Wei, Feng, Shejun, Ji, Xunming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804044/
https://www.ncbi.nlm.nih.gov/pubmed/36341958
http://dx.doi.org/10.1111/cns.14017
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author Liu, Liqiang
Liu, Jia
Li, Ming
Lyu, Junxuan
Su, Wei
Feng, Shejun
Ji, Xunming
author_facet Liu, Liqiang
Liu, Jia
Li, Ming
Lyu, Junxuan
Su, Wei
Feng, Shejun
Ji, Xunming
author_sort Liu, Liqiang
collection PubMed
description AIMS: This study aimed to investigate the effects of mild selective brain hypothermia on aged female ischemic mice. METHODS: A distal middle cerebral artery occlusion (dMCAO) model was established in aged female mice, who were then subjected to mild selective brain hypothermia immediately after the dMCAO procedure. Neurological behavioral examinations were conducted prior to and up to 35 days post‐ischemia. Infarct volume, brain atrophy, pro‐inflammation, and anti‐inflammation microglia/macrophages phenotype and white matter injury were evaluated by immunofluorescence staining. Correlations between neurological behaviors and histological parameters were evaluated by Pearson product linear regression analysis. RESULTS: Sensorimotor and cognitive function tests confirmed the protective effect of mild selective brain hypothermia in elderly female ischemic mice. In addition, hypothermia decreased the infarct volume and brain atrophy induced by focal cerebral ischemia. Furthermore, hypothermia alleviated ischemia‐induced short‐term and long‐term white matter injury, which was correlated with behavioral deficits. Finally, hypothermia suppressed the harmful immunological response by promoting the transformation of pro‐inflammatory microglia/macrophages to anti‐inflammatory phenotype. This polarization was negatively correlated with neuronal loss and white matter injury. CONCLUSION: Mild selective brain hypothermia promoted long‐term functional recovery by alleviating white matter damage in an aged female mouse model of ischemia.
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spelling pubmed-98040442023-01-04 Selective brain hypothermia attenuates focal cerebral ischemic injury and improves long‐term neurological outcome in aged female mice Liu, Liqiang Liu, Jia Li, Ming Lyu, Junxuan Su, Wei Feng, Shejun Ji, Xunming CNS Neurosci Ther Original Articles AIMS: This study aimed to investigate the effects of mild selective brain hypothermia on aged female ischemic mice. METHODS: A distal middle cerebral artery occlusion (dMCAO) model was established in aged female mice, who were then subjected to mild selective brain hypothermia immediately after the dMCAO procedure. Neurological behavioral examinations were conducted prior to and up to 35 days post‐ischemia. Infarct volume, brain atrophy, pro‐inflammation, and anti‐inflammation microglia/macrophages phenotype and white matter injury were evaluated by immunofluorescence staining. Correlations between neurological behaviors and histological parameters were evaluated by Pearson product linear regression analysis. RESULTS: Sensorimotor and cognitive function tests confirmed the protective effect of mild selective brain hypothermia in elderly female ischemic mice. In addition, hypothermia decreased the infarct volume and brain atrophy induced by focal cerebral ischemia. Furthermore, hypothermia alleviated ischemia‐induced short‐term and long‐term white matter injury, which was correlated with behavioral deficits. Finally, hypothermia suppressed the harmful immunological response by promoting the transformation of pro‐inflammatory microglia/macrophages to anti‐inflammatory phenotype. This polarization was negatively correlated with neuronal loss and white matter injury. CONCLUSION: Mild selective brain hypothermia promoted long‐term functional recovery by alleviating white matter damage in an aged female mouse model of ischemia. John Wiley and Sons Inc. 2022-11-07 /pmc/articles/PMC9804044/ /pubmed/36341958 http://dx.doi.org/10.1111/cns.14017 Text en © 2022 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Liu, Liqiang
Liu, Jia
Li, Ming
Lyu, Junxuan
Su, Wei
Feng, Shejun
Ji, Xunming
Selective brain hypothermia attenuates focal cerebral ischemic injury and improves long‐term neurological outcome in aged female mice
title Selective brain hypothermia attenuates focal cerebral ischemic injury and improves long‐term neurological outcome in aged female mice
title_full Selective brain hypothermia attenuates focal cerebral ischemic injury and improves long‐term neurological outcome in aged female mice
title_fullStr Selective brain hypothermia attenuates focal cerebral ischemic injury and improves long‐term neurological outcome in aged female mice
title_full_unstemmed Selective brain hypothermia attenuates focal cerebral ischemic injury and improves long‐term neurological outcome in aged female mice
title_short Selective brain hypothermia attenuates focal cerebral ischemic injury and improves long‐term neurological outcome in aged female mice
title_sort selective brain hypothermia attenuates focal cerebral ischemic injury and improves long‐term neurological outcome in aged female mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804044/
https://www.ncbi.nlm.nih.gov/pubmed/36341958
http://dx.doi.org/10.1111/cns.14017
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