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Impaired microcirculation after subarachnoid hemorrhage in an in vivo animal model
The influence of aneurysmal subarachnoid hemorrhage (SAH) on brain microcirculation has not yet been systematically investigated. We established an animal model to examine (1) the brain surface microcirculation (2) the influences of cerebrospinal fluid (CSF) from aneurysmal SAH on the brain surface...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127197/ https://www.ncbi.nlm.nih.gov/pubmed/30190518 http://dx.doi.org/10.1038/s41598-018-31709-7 |
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author | Wang, Kuo-Chuan Tang, Sung-Chun Lee, Jing-Er Tsai, Jui-Chang Lai, Dar-Ming Lin, Wei-Chou Lin, Chih-Peng Tu, Yong-Kwang Hsieh, Sung-Tsang |
author_facet | Wang, Kuo-Chuan Tang, Sung-Chun Lee, Jing-Er Tsai, Jui-Chang Lai, Dar-Ming Lin, Wei-Chou Lin, Chih-Peng Tu, Yong-Kwang Hsieh, Sung-Tsang |
author_sort | Wang, Kuo-Chuan |
collection | PubMed |
description | The influence of aneurysmal subarachnoid hemorrhage (SAH) on brain microcirculation has not yet been systematically investigated. We established an animal model to examine (1) the brain surface microcirculation (2) the influences of cerebrospinal fluid (CSF) from aneurysmal SAH on the brain surface microcirculation. A rat SAH model was induced by injection of autologous arterial blood into the cisterna magnum, and the brain surface microcirculation was evaluated by a capillary videoscope with craniotomy at the fronto-parietal region. CSF from SAH rats and SAH patients was applied on the brain surface of naïve rats to assess the resulting microcirculatory changes. In the SAH rats, diffuse constriction of cortical arterioles within 24 hours of SAH was observed. Similar patterns of microcirculation impairment were induced on normal rat brain surfaces via application of CSF from SAH rats and SAH patients. Furthermore, the proportion of subjects with arteriolar vasoconstriction was significantly higher in the group of SAH patients with delayed ischemic neurological deficits (DIND) than in those without DIND (p < 0.001). This study demonstrated impaired microcirculation on brain surface arterioles in a rat model of SAH. CSF from SAH rats and patients was responsible for impairment of brain surface microcirculation. |
format | Online Article Text |
id | pubmed-6127197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61271972018-09-10 Impaired microcirculation after subarachnoid hemorrhage in an in vivo animal model Wang, Kuo-Chuan Tang, Sung-Chun Lee, Jing-Er Tsai, Jui-Chang Lai, Dar-Ming Lin, Wei-Chou Lin, Chih-Peng Tu, Yong-Kwang Hsieh, Sung-Tsang Sci Rep Article The influence of aneurysmal subarachnoid hemorrhage (SAH) on brain microcirculation has not yet been systematically investigated. We established an animal model to examine (1) the brain surface microcirculation (2) the influences of cerebrospinal fluid (CSF) from aneurysmal SAH on the brain surface microcirculation. A rat SAH model was induced by injection of autologous arterial blood into the cisterna magnum, and the brain surface microcirculation was evaluated by a capillary videoscope with craniotomy at the fronto-parietal region. CSF from SAH rats and SAH patients was applied on the brain surface of naïve rats to assess the resulting microcirculatory changes. In the SAH rats, diffuse constriction of cortical arterioles within 24 hours of SAH was observed. Similar patterns of microcirculation impairment were induced on normal rat brain surfaces via application of CSF from SAH rats and SAH patients. Furthermore, the proportion of subjects with arteriolar vasoconstriction was significantly higher in the group of SAH patients with delayed ischemic neurological deficits (DIND) than in those without DIND (p < 0.001). This study demonstrated impaired microcirculation on brain surface arterioles in a rat model of SAH. CSF from SAH rats and patients was responsible for impairment of brain surface microcirculation. Nature Publishing Group UK 2018-09-06 /pmc/articles/PMC6127197/ /pubmed/30190518 http://dx.doi.org/10.1038/s41598-018-31709-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Kuo-Chuan Tang, Sung-Chun Lee, Jing-Er Tsai, Jui-Chang Lai, Dar-Ming Lin, Wei-Chou Lin, Chih-Peng Tu, Yong-Kwang Hsieh, Sung-Tsang Impaired microcirculation after subarachnoid hemorrhage in an in vivo animal model |
title | Impaired microcirculation after subarachnoid hemorrhage in an in vivo animal model |
title_full | Impaired microcirculation after subarachnoid hemorrhage in an in vivo animal model |
title_fullStr | Impaired microcirculation after subarachnoid hemorrhage in an in vivo animal model |
title_full_unstemmed | Impaired microcirculation after subarachnoid hemorrhage in an in vivo animal model |
title_short | Impaired microcirculation after subarachnoid hemorrhage in an in vivo animal model |
title_sort | impaired microcirculation after subarachnoid hemorrhage in an in vivo animal model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127197/ https://www.ncbi.nlm.nih.gov/pubmed/30190518 http://dx.doi.org/10.1038/s41598-018-31709-7 |
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