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Nanometer ultrastructural brain damage following low intensity primary blast wave exposure
Blast-induced mild traumatic brain injury (mTBI) is of particular concern among military personnel due to exposure to blast energy during military training and combat. The impact of primary low-intensity blast mediated pathophysiology upon later neurobehavioral disorders has been controversial. Deve...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126131/ https://www.ncbi.nlm.nih.gov/pubmed/30127104 http://dx.doi.org/10.4103/1673-5374.237110 |
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author | Song, Hailong Konan, Landry M. Cui, Jiankun Johnson, Catherine E. Hubler, Graham K. DePalma, Ralph G. Gu, Zezong |
author_facet | Song, Hailong Konan, Landry M. Cui, Jiankun Johnson, Catherine E. Hubler, Graham K. DePalma, Ralph G. Gu, Zezong |
author_sort | Song, Hailong |
collection | PubMed |
description | Blast-induced mild traumatic brain injury (mTBI) is of particular concern among military personnel due to exposure to blast energy during military training and combat. The impact of primary low-intensity blast mediated pathophysiology upon later neurobehavioral disorders has been controversial. Developing a military preclinical blast model to simulate the pathophysiology of human blast injury is an important first step. This article provides an overview of primary blast effects and perspectives of our recent studies demonstrating ultrastructural changes in the brain and behavioral disorders resulting from open-field blast exposures up to 46.6 kPa using a murine model. The model is scalable and permits exposure to varying magnitudes of primary blast injuries by placing animals at different distances from the blast center or by changing the amount of C4 charge. We here review the implications and future applications and directions of using this animal model to uncover the underlying mechanisms related to primary blast injury. Overall, these studies offer the prospect of enhanced understanding of the pathogenesis of primary low-intensity blast-induced TBI and insights for prevention, diagnosis and treatment of blast induced TBI, particularly mTBI/concussion related to current combat exposures. |
format | Online Article Text |
id | pubmed-6126131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61261312018-09-12 Nanometer ultrastructural brain damage following low intensity primary blast wave exposure Song, Hailong Konan, Landry M. Cui, Jiankun Johnson, Catherine E. Hubler, Graham K. DePalma, Ralph G. Gu, Zezong Neural Regen Res Review Blast-induced mild traumatic brain injury (mTBI) is of particular concern among military personnel due to exposure to blast energy during military training and combat. The impact of primary low-intensity blast mediated pathophysiology upon later neurobehavioral disorders has been controversial. Developing a military preclinical blast model to simulate the pathophysiology of human blast injury is an important first step. This article provides an overview of primary blast effects and perspectives of our recent studies demonstrating ultrastructural changes in the brain and behavioral disorders resulting from open-field blast exposures up to 46.6 kPa using a murine model. The model is scalable and permits exposure to varying magnitudes of primary blast injuries by placing animals at different distances from the blast center or by changing the amount of C4 charge. We here review the implications and future applications and directions of using this animal model to uncover the underlying mechanisms related to primary blast injury. Overall, these studies offer the prospect of enhanced understanding of the pathogenesis of primary low-intensity blast-induced TBI and insights for prevention, diagnosis and treatment of blast induced TBI, particularly mTBI/concussion related to current combat exposures. Medknow Publications & Media Pvt Ltd 2018-09 /pmc/articles/PMC6126131/ /pubmed/30127104 http://dx.doi.org/10.4103/1673-5374.237110 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Review Song, Hailong Konan, Landry M. Cui, Jiankun Johnson, Catherine E. Hubler, Graham K. DePalma, Ralph G. Gu, Zezong Nanometer ultrastructural brain damage following low intensity primary blast wave exposure |
title | Nanometer ultrastructural brain damage following low intensity primary blast wave exposure |
title_full | Nanometer ultrastructural brain damage following low intensity primary blast wave exposure |
title_fullStr | Nanometer ultrastructural brain damage following low intensity primary blast wave exposure |
title_full_unstemmed | Nanometer ultrastructural brain damage following low intensity primary blast wave exposure |
title_short | Nanometer ultrastructural brain damage following low intensity primary blast wave exposure |
title_sort | nanometer ultrastructural brain damage following low intensity primary blast wave exposure |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126131/ https://www.ncbi.nlm.nih.gov/pubmed/30127104 http://dx.doi.org/10.4103/1673-5374.237110 |
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