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DHA Attenuates Cerebral Edema Following Traumatic Brain Injury via the Reduction in Blood–Brain Barrier Permeability

Traumatic brain injury (TBI) could result in edema and cause an increase in intracranial pressure of the brain resulting in mortality and morbidity. Although there is hyperosmolarity therapy available for this pathophysiological event, it remains controversial. Recently, several groups have shown do...

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Autores principales: Liu, Zhuo-Hao, Chen, Nan-Yu, Tu, Po-hsun, Wu, Chen-Te, Chiu, Shao-Chieh, Huang, Ying-Cheng, Lim, Siew-Na, Yip, Ping K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503959/
https://www.ncbi.nlm.nih.gov/pubmed/32878052
http://dx.doi.org/10.3390/ijms21176291
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author Liu, Zhuo-Hao
Chen, Nan-Yu
Tu, Po-hsun
Wu, Chen-Te
Chiu, Shao-Chieh
Huang, Ying-Cheng
Lim, Siew-Na
Yip, Ping K.
author_facet Liu, Zhuo-Hao
Chen, Nan-Yu
Tu, Po-hsun
Wu, Chen-Te
Chiu, Shao-Chieh
Huang, Ying-Cheng
Lim, Siew-Na
Yip, Ping K.
author_sort Liu, Zhuo-Hao
collection PubMed
description Traumatic brain injury (TBI) could result in edema and cause an increase in intracranial pressure of the brain resulting in mortality and morbidity. Although there is hyperosmolarity therapy available for this pathophysiological event, it remains controversial. Recently, several groups have shown docosahexaenoic acid (DHA) to improve functional and histological outcomes following brain injury based on reduction of neuroinflammation and apoptosis. However, the effect of DHA on blood–brain barrier (BBB) dysfunction after brain injury has not been fully studied. Here, a controlled cortical impact rat model was used to test the effect of a single dose of DHA administered 30 min post injury. Modified neurological severity score (mNSS) and forelimb asymmetry were used to determine the functional outcomes. Neuroimaging and histology were used to characterize the edema and BBB dysfunction. The study showed that DHA-treated TBI rats had better mNSS and forelimb asymmetry score than vehicle-treated TBI rats. Temporal analysis of edema using MRI revealed a significant reduction in edema level with DHA treatment compared to vehicle in TBI rats. Histological analysis using immunoglobulin G (IgG) extravasation showed that there was less extravasation, which corresponded with a reduction in aquaporin 4 and astrocytic metalloprotease 9 expression, and greater endothelial occludin expression in the peri-contusional site of the TBI rat brain treated with DHA in comparison to vehicle treatment. In conclusion, the study shows that DHA can exert its functional improvement by prevention of the edema formation via prevention of BBB dysfunction after TBI.
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spelling pubmed-75039592020-09-27 DHA Attenuates Cerebral Edema Following Traumatic Brain Injury via the Reduction in Blood–Brain Barrier Permeability Liu, Zhuo-Hao Chen, Nan-Yu Tu, Po-hsun Wu, Chen-Te Chiu, Shao-Chieh Huang, Ying-Cheng Lim, Siew-Na Yip, Ping K. Int J Mol Sci Article Traumatic brain injury (TBI) could result in edema and cause an increase in intracranial pressure of the brain resulting in mortality and morbidity. Although there is hyperosmolarity therapy available for this pathophysiological event, it remains controversial. Recently, several groups have shown docosahexaenoic acid (DHA) to improve functional and histological outcomes following brain injury based on reduction of neuroinflammation and apoptosis. However, the effect of DHA on blood–brain barrier (BBB) dysfunction after brain injury has not been fully studied. Here, a controlled cortical impact rat model was used to test the effect of a single dose of DHA administered 30 min post injury. Modified neurological severity score (mNSS) and forelimb asymmetry were used to determine the functional outcomes. Neuroimaging and histology were used to characterize the edema and BBB dysfunction. The study showed that DHA-treated TBI rats had better mNSS and forelimb asymmetry score than vehicle-treated TBI rats. Temporal analysis of edema using MRI revealed a significant reduction in edema level with DHA treatment compared to vehicle in TBI rats. Histological analysis using immunoglobulin G (IgG) extravasation showed that there was less extravasation, which corresponded with a reduction in aquaporin 4 and astrocytic metalloprotease 9 expression, and greater endothelial occludin expression in the peri-contusional site of the TBI rat brain treated with DHA in comparison to vehicle treatment. In conclusion, the study shows that DHA can exert its functional improvement by prevention of the edema formation via prevention of BBB dysfunction after TBI. MDPI 2020-08-31 /pmc/articles/PMC7503959/ /pubmed/32878052 http://dx.doi.org/10.3390/ijms21176291 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Zhuo-Hao
Chen, Nan-Yu
Tu, Po-hsun
Wu, Chen-Te
Chiu, Shao-Chieh
Huang, Ying-Cheng
Lim, Siew-Na
Yip, Ping K.
DHA Attenuates Cerebral Edema Following Traumatic Brain Injury via the Reduction in Blood–Brain Barrier Permeability
title DHA Attenuates Cerebral Edema Following Traumatic Brain Injury via the Reduction in Blood–Brain Barrier Permeability
title_full DHA Attenuates Cerebral Edema Following Traumatic Brain Injury via the Reduction in Blood–Brain Barrier Permeability
title_fullStr DHA Attenuates Cerebral Edema Following Traumatic Brain Injury via the Reduction in Blood–Brain Barrier Permeability
title_full_unstemmed DHA Attenuates Cerebral Edema Following Traumatic Brain Injury via the Reduction in Blood–Brain Barrier Permeability
title_short DHA Attenuates Cerebral Edema Following Traumatic Brain Injury via the Reduction in Blood–Brain Barrier Permeability
title_sort dha attenuates cerebral edema following traumatic brain injury via the reduction in blood–brain barrier permeability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503959/
https://www.ncbi.nlm.nih.gov/pubmed/32878052
http://dx.doi.org/10.3390/ijms21176291
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