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Transient filament occlusion of the middle cerebral artery in rats: does the reperfusion method matter 24 hours after perfusion?
BACKGROUND: There are two widely used transient middle cerebral artery occlusion (MCAO) methods, which differ in the use of unilateral or bilateral carotid artery reperfusion (UNICAR and BICAR). Of the two methods, UNICAR is easier to perform. This study was designed to comprehensively compare the t...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546945/ https://www.ncbi.nlm.nih.gov/pubmed/23272656 http://dx.doi.org/10.1186/1471-2202-13-154 |
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author | Liu, Jian-Ren Jensen-Kondering, Ulf R Zhou, Jia-Jun Sun, Fen Feng, Xiao-Yan Shen, Xiao-Lei Deuschl, Günther Jansen, Olav Herdegen, Thomas Meyne, Johannes Zhao, Yi Eschenfelder, Christoph |
author_facet | Liu, Jian-Ren Jensen-Kondering, Ulf R Zhou, Jia-Jun Sun, Fen Feng, Xiao-Yan Shen, Xiao-Lei Deuschl, Günther Jansen, Olav Herdegen, Thomas Meyne, Johannes Zhao, Yi Eschenfelder, Christoph |
author_sort | Liu, Jian-Ren |
collection | PubMed |
description | BACKGROUND: There are two widely used transient middle cerebral artery occlusion (MCAO) methods, which differ in the use of unilateral or bilateral carotid artery reperfusion (UNICAR and BICAR). Of the two methods, UNICAR is easier to perform. This study was designed to comprehensively compare the two reperfusion methods to determine if there are any differences in outcomes. RESULTS: The UNICAR and BICAR groups each included 9 rats. At baseline, the average pO(2) was 20.54 ± 9.35 and 26.43 ± 7.39, for the UNICAR and BICAR groups, respectively (P = 0.519). Changes in pO(2), as well as other physiological parameters measured within the ischemic lesion, were similar between the UNICAR and BICAR groups during 90 min of MCAO and the first 30 min of reperfusion (all P > 0.05). Furthermore, both the Bederson score and Garcia score, which are used for neurological assessment, were also similar (both P > 0.05). There were also no significant differences in T2WI lesion volume, DWI lesion volume, PWI lesion volume, or TTC staining infarct volume between the two groups (all P > 0.05). CONCLUSION: UNICAR and BICAR have similar capability for inducing acute brain ischemic injury and can be considered interchangeable up to 24 hours after reperfusion. |
format | Online Article Text |
id | pubmed-3546945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35469452013-01-17 Transient filament occlusion of the middle cerebral artery in rats: does the reperfusion method matter 24 hours after perfusion? Liu, Jian-Ren Jensen-Kondering, Ulf R Zhou, Jia-Jun Sun, Fen Feng, Xiao-Yan Shen, Xiao-Lei Deuschl, Günther Jansen, Olav Herdegen, Thomas Meyne, Johannes Zhao, Yi Eschenfelder, Christoph BMC Neurosci Research Article BACKGROUND: There are two widely used transient middle cerebral artery occlusion (MCAO) methods, which differ in the use of unilateral or bilateral carotid artery reperfusion (UNICAR and BICAR). Of the two methods, UNICAR is easier to perform. This study was designed to comprehensively compare the two reperfusion methods to determine if there are any differences in outcomes. RESULTS: The UNICAR and BICAR groups each included 9 rats. At baseline, the average pO(2) was 20.54 ± 9.35 and 26.43 ± 7.39, for the UNICAR and BICAR groups, respectively (P = 0.519). Changes in pO(2), as well as other physiological parameters measured within the ischemic lesion, were similar between the UNICAR and BICAR groups during 90 min of MCAO and the first 30 min of reperfusion (all P > 0.05). Furthermore, both the Bederson score and Garcia score, which are used for neurological assessment, were also similar (both P > 0.05). There were also no significant differences in T2WI lesion volume, DWI lesion volume, PWI lesion volume, or TTC staining infarct volume between the two groups (all P > 0.05). CONCLUSION: UNICAR and BICAR have similar capability for inducing acute brain ischemic injury and can be considered interchangeable up to 24 hours after reperfusion. BioMed Central 2012-12-29 /pmc/articles/PMC3546945/ /pubmed/23272656 http://dx.doi.org/10.1186/1471-2202-13-154 Text en Copyright ©2012 Liu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Liu, Jian-Ren Jensen-Kondering, Ulf R Zhou, Jia-Jun Sun, Fen Feng, Xiao-Yan Shen, Xiao-Lei Deuschl, Günther Jansen, Olav Herdegen, Thomas Meyne, Johannes Zhao, Yi Eschenfelder, Christoph Transient filament occlusion of the middle cerebral artery in rats: does the reperfusion method matter 24 hours after perfusion? |
title | Transient filament occlusion of the middle cerebral artery in rats: does the reperfusion method matter 24 hours after perfusion? |
title_full | Transient filament occlusion of the middle cerebral artery in rats: does the reperfusion method matter 24 hours after perfusion? |
title_fullStr | Transient filament occlusion of the middle cerebral artery in rats: does the reperfusion method matter 24 hours after perfusion? |
title_full_unstemmed | Transient filament occlusion of the middle cerebral artery in rats: does the reperfusion method matter 24 hours after perfusion? |
title_short | Transient filament occlusion of the middle cerebral artery in rats: does the reperfusion method matter 24 hours after perfusion? |
title_sort | transient filament occlusion of the middle cerebral artery in rats: does the reperfusion method matter 24 hours after perfusion? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546945/ https://www.ncbi.nlm.nih.gov/pubmed/23272656 http://dx.doi.org/10.1186/1471-2202-13-154 |
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