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Neuronal and glial changes in the brain resulting from explosive blast in an experimental model

Mild traumatic brain injury (mTBI) is the signature injury in warfighters exposed to explosive blasts. The pathology underlying mTBI is poorly understood, as this condition is rarely fatal and thus postmortem brains are difficult to obtain for neuropathological studies. Here we report on studies of...

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Autores principales: Goodrich, James A., Kim, Jung H., Situ, Robert, Taylor, Wesley, Westmoreland, Ted, Du, Fu, Parks, Steven, Ling, Geoffrey, Hwang, Jung Y., Rapuano, Amedeo, Bandak, Faris A., de Lanerolle, Nihal C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123270/
https://www.ncbi.nlm.nih.gov/pubmed/27884214
http://dx.doi.org/10.1186/s40478-016-0395-3
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author Goodrich, James A.
Kim, Jung H.
Situ, Robert
Taylor, Wesley
Westmoreland, Ted
Du, Fu
Parks, Steven
Ling, Geoffrey
Hwang, Jung Y.
Rapuano, Amedeo
Bandak, Faris A.
de Lanerolle, Nihal C.
author_facet Goodrich, James A.
Kim, Jung H.
Situ, Robert
Taylor, Wesley
Westmoreland, Ted
Du, Fu
Parks, Steven
Ling, Geoffrey
Hwang, Jung Y.
Rapuano, Amedeo
Bandak, Faris A.
de Lanerolle, Nihal C.
author_sort Goodrich, James A.
collection PubMed
description Mild traumatic brain injury (mTBI) is the signature injury in warfighters exposed to explosive blasts. The pathology underlying mTBI is poorly understood, as this condition is rarely fatal and thus postmortem brains are difficult to obtain for neuropathological studies. Here we report on studies of an experimental model with a gyrencephalic brain that is exposed to single and multiple explosive blast pressure waves. To determine injuries to the brain resulting from the primary blast, experimental conditions were controlled to eliminate any secondary or tertiary injury from blasts. We found small but significant levels of neuronal loss in the hippocampus, a brain area that is important for cognitive functions. Furthermore, neuronal loss increased with multiple blasts and the degree of neuronal injury worsened with time post-blast. This is consistent with our findings in the blast-exposed human brain based on magnetic resonance spectroscopic imaging. The studies on this experimental model thus confirm what has been presumed to be the case with the warfighter, namely that exposure to multiple blasts causes increased brain injury. Additionally, as in other studies of both explosive blast as well as closed head mTBI, we found astrocyte activation. Activated microglia were also prominent in white matter tracts, particularly in animals exposed to multiple blasts and at long post-blast intervals, even though injured axons (i.e. β-APP positive) were not found in these areas. Microglial activation appears to be a delayed response, though whether they may contribute to inflammation related injury mechanism at even longer post-blast times than we tested here, remains to be explored. Petechial hemorrhages or other gross signs of vascular injury were not observed in our study. These findings confirm the development of neuropathological changes due to blast exposure. The activation of astrocytes and microglia, cell types potentially involved in inflammatory processes, suggest an important area for future study.
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spelling pubmed-51232702016-12-06 Neuronal and glial changes in the brain resulting from explosive blast in an experimental model Goodrich, James A. Kim, Jung H. Situ, Robert Taylor, Wesley Westmoreland, Ted Du, Fu Parks, Steven Ling, Geoffrey Hwang, Jung Y. Rapuano, Amedeo Bandak, Faris A. de Lanerolle, Nihal C. Acta Neuropathol Commun Research Mild traumatic brain injury (mTBI) is the signature injury in warfighters exposed to explosive blasts. The pathology underlying mTBI is poorly understood, as this condition is rarely fatal and thus postmortem brains are difficult to obtain for neuropathological studies. Here we report on studies of an experimental model with a gyrencephalic brain that is exposed to single and multiple explosive blast pressure waves. To determine injuries to the brain resulting from the primary blast, experimental conditions were controlled to eliminate any secondary or tertiary injury from blasts. We found small but significant levels of neuronal loss in the hippocampus, a brain area that is important for cognitive functions. Furthermore, neuronal loss increased with multiple blasts and the degree of neuronal injury worsened with time post-blast. This is consistent with our findings in the blast-exposed human brain based on magnetic resonance spectroscopic imaging. The studies on this experimental model thus confirm what has been presumed to be the case with the warfighter, namely that exposure to multiple blasts causes increased brain injury. Additionally, as in other studies of both explosive blast as well as closed head mTBI, we found astrocyte activation. Activated microglia were also prominent in white matter tracts, particularly in animals exposed to multiple blasts and at long post-blast intervals, even though injured axons (i.e. β-APP positive) were not found in these areas. Microglial activation appears to be a delayed response, though whether they may contribute to inflammation related injury mechanism at even longer post-blast times than we tested here, remains to be explored. Petechial hemorrhages or other gross signs of vascular injury were not observed in our study. These findings confirm the development of neuropathological changes due to blast exposure. The activation of astrocytes and microglia, cell types potentially involved in inflammatory processes, suggest an important area for future study. BioMed Central 2016-11-24 /pmc/articles/PMC5123270/ /pubmed/27884214 http://dx.doi.org/10.1186/s40478-016-0395-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Goodrich, James A.
Kim, Jung H.
Situ, Robert
Taylor, Wesley
Westmoreland, Ted
Du, Fu
Parks, Steven
Ling, Geoffrey
Hwang, Jung Y.
Rapuano, Amedeo
Bandak, Faris A.
de Lanerolle, Nihal C.
Neuronal and glial changes in the brain resulting from explosive blast in an experimental model
title Neuronal and glial changes in the brain resulting from explosive blast in an experimental model
title_full Neuronal and glial changes in the brain resulting from explosive blast in an experimental model
title_fullStr Neuronal and glial changes in the brain resulting from explosive blast in an experimental model
title_full_unstemmed Neuronal and glial changes in the brain resulting from explosive blast in an experimental model
title_short Neuronal and glial changes in the brain resulting from explosive blast in an experimental model
title_sort neuronal and glial changes in the brain resulting from explosive blast in an experimental model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123270/
https://www.ncbi.nlm.nih.gov/pubmed/27884214
http://dx.doi.org/10.1186/s40478-016-0395-3
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