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Blast-induced temporal alterations in blood–brain barrier properties in a rodent model
The consequences of blast-induced traumatic brain injury (bTBI) on the blood–brain barrier (BBB) and components of the neurovascular unit are an area of active research. In this study we assessed the time course of BBB integrity in anesthetized rats exposed to a single blast overpressure of 130 kPa...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971015/ https://www.ncbi.nlm.nih.gov/pubmed/33723300 http://dx.doi.org/10.1038/s41598-021-84730-8 |
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author | Kawoos, Usmah Abutarboush, Rania Gu, Ming Chen, Ye Statz, Jonathan K. Goodrich, Samantha Y. Ahlers, Stephen T. |
author_facet | Kawoos, Usmah Abutarboush, Rania Gu, Ming Chen, Ye Statz, Jonathan K. Goodrich, Samantha Y. Ahlers, Stephen T. |
author_sort | Kawoos, Usmah |
collection | PubMed |
description | The consequences of blast-induced traumatic brain injury (bTBI) on the blood–brain barrier (BBB) and components of the neurovascular unit are an area of active research. In this study we assessed the time course of BBB integrity in anesthetized rats exposed to a single blast overpressure of 130 kPa (18.9 PSI). BBB permeability was measured in vivo via intravital microscopy by imaging extravasation of fluorescently labeled tracers (40 kDa and 70 kDa molecular weight) through the pial microvasculature into brain parenchyma at 2–3 h, 1, 3, 14, or 28 days after the blast exposure. BBB structural changes were assessed by immunostaining and molecular assays. At 2–3 h and 1 day after blast exposure, significant increases in the extravasation of the 40 kDa but not the 70 kDa tracers were observed, along with differential reductions in the expression of tight junction proteins (occludin, claudin-5, zona occluden-1) and increase in the levels of the astrocytic water channel protein, AQP-4, and matrix metalloprotease, MMP-9. Nearly all of these measures were normalized by day 3 and maintained up to 28 days post exposure. These data demonstrate that blast-induced changes in BBB permeability are closely coupled to structural and functional components of the BBB. |
format | Online Article Text |
id | pubmed-7971015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79710152021-03-19 Blast-induced temporal alterations in blood–brain barrier properties in a rodent model Kawoos, Usmah Abutarboush, Rania Gu, Ming Chen, Ye Statz, Jonathan K. Goodrich, Samantha Y. Ahlers, Stephen T. Sci Rep Article The consequences of blast-induced traumatic brain injury (bTBI) on the blood–brain barrier (BBB) and components of the neurovascular unit are an area of active research. In this study we assessed the time course of BBB integrity in anesthetized rats exposed to a single blast overpressure of 130 kPa (18.9 PSI). BBB permeability was measured in vivo via intravital microscopy by imaging extravasation of fluorescently labeled tracers (40 kDa and 70 kDa molecular weight) through the pial microvasculature into brain parenchyma at 2–3 h, 1, 3, 14, or 28 days after the blast exposure. BBB structural changes were assessed by immunostaining and molecular assays. At 2–3 h and 1 day after blast exposure, significant increases in the extravasation of the 40 kDa but not the 70 kDa tracers were observed, along with differential reductions in the expression of tight junction proteins (occludin, claudin-5, zona occluden-1) and increase in the levels of the astrocytic water channel protein, AQP-4, and matrix metalloprotease, MMP-9. Nearly all of these measures were normalized by day 3 and maintained up to 28 days post exposure. These data demonstrate that blast-induced changes in BBB permeability are closely coupled to structural and functional components of the BBB. Nature Publishing Group UK 2021-03-15 /pmc/articles/PMC7971015/ /pubmed/33723300 http://dx.doi.org/10.1038/s41598-021-84730-8 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kawoos, Usmah Abutarboush, Rania Gu, Ming Chen, Ye Statz, Jonathan K. Goodrich, Samantha Y. Ahlers, Stephen T. Blast-induced temporal alterations in blood–brain barrier properties in a rodent model |
title | Blast-induced temporal alterations in blood–brain barrier properties in a rodent model |
title_full | Blast-induced temporal alterations in blood–brain barrier properties in a rodent model |
title_fullStr | Blast-induced temporal alterations in blood–brain barrier properties in a rodent model |
title_full_unstemmed | Blast-induced temporal alterations in blood–brain barrier properties in a rodent model |
title_short | Blast-induced temporal alterations in blood–brain barrier properties in a rodent model |
title_sort | blast-induced temporal alterations in blood–brain barrier properties in a rodent model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971015/ https://www.ncbi.nlm.nih.gov/pubmed/33723300 http://dx.doi.org/10.1038/s41598-021-84730-8 |
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