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Time course of blast-induced injury in the rat auditory cortex
Blast exposure is an increasingly significant health hazard and can have a range of debilitating effects, including auditory dysfunction and traumatic brain injury. To assist in the development of effective treatments, a greater understanding of the mechanisms of blast-induced auditory damage and dy...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831391/ https://www.ncbi.nlm.nih.gov/pubmed/29489862 http://dx.doi.org/10.1371/journal.pone.0193389 |
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author | Kallakuri, Srinivasu Pace, Edward Lu, Huichao Luo, Hao Cavanaugh, John Zhang, Jinsheng |
author_facet | Kallakuri, Srinivasu Pace, Edward Lu, Huichao Luo, Hao Cavanaugh, John Zhang, Jinsheng |
author_sort | Kallakuri, Srinivasu |
collection | PubMed |
description | Blast exposure is an increasingly significant health hazard and can have a range of debilitating effects, including auditory dysfunction and traumatic brain injury. To assist in the development of effective treatments, a greater understanding of the mechanisms of blast-induced auditory damage and dysfunction, especially in the central nervous system, is critical. To elucidate this area, we subjected rats to a unilateral blast exposure at 22 psi, measured their auditory brainstem responses (ABRs), and histologically processed their brains at 1 day, 1 month, and 3-month survival time points. The left and right auditory cortices was assessed for astrocytic reactivity and axonal degenerative changes using glial fibrillary acidic protein immunoreactivity and a silver impregnation technique, respectively. Although only unilateral hearing loss was induced, astrocytosis was bilaterally elevated at 1 month post-blast exposure compared to shams, and showed a positive trend of elevation at 3 months post-blast. Axonal degeneration, on the other hand, appeared to be more robust at 1 day and 3 months post-blast. Interestingly, while ABR threshold shifts recovered by the 1 and 3-month time-points, a positive correlation was observed between rats’ astrocyte counts at 1 month post-blast and their threshold shifts at 1 day post-blast. Taken together, our findings suggest that central auditory damage may have occurred due to biomechanical forces from the blast shockwave, and that different indicators/types of damage may manifest over different timelines. |
format | Online Article Text |
id | pubmed-5831391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58313912018-03-19 Time course of blast-induced injury in the rat auditory cortex Kallakuri, Srinivasu Pace, Edward Lu, Huichao Luo, Hao Cavanaugh, John Zhang, Jinsheng PLoS One Research Article Blast exposure is an increasingly significant health hazard and can have a range of debilitating effects, including auditory dysfunction and traumatic brain injury. To assist in the development of effective treatments, a greater understanding of the mechanisms of blast-induced auditory damage and dysfunction, especially in the central nervous system, is critical. To elucidate this area, we subjected rats to a unilateral blast exposure at 22 psi, measured their auditory brainstem responses (ABRs), and histologically processed their brains at 1 day, 1 month, and 3-month survival time points. The left and right auditory cortices was assessed for astrocytic reactivity and axonal degenerative changes using glial fibrillary acidic protein immunoreactivity and a silver impregnation technique, respectively. Although only unilateral hearing loss was induced, astrocytosis was bilaterally elevated at 1 month post-blast exposure compared to shams, and showed a positive trend of elevation at 3 months post-blast. Axonal degeneration, on the other hand, appeared to be more robust at 1 day and 3 months post-blast. Interestingly, while ABR threshold shifts recovered by the 1 and 3-month time-points, a positive correlation was observed between rats’ astrocyte counts at 1 month post-blast and their threshold shifts at 1 day post-blast. Taken together, our findings suggest that central auditory damage may have occurred due to biomechanical forces from the blast shockwave, and that different indicators/types of damage may manifest over different timelines. Public Library of Science 2018-02-28 /pmc/articles/PMC5831391/ /pubmed/29489862 http://dx.doi.org/10.1371/journal.pone.0193389 Text en © 2018 Kallakuri et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kallakuri, Srinivasu Pace, Edward Lu, Huichao Luo, Hao Cavanaugh, John Zhang, Jinsheng Time course of blast-induced injury in the rat auditory cortex |
title | Time course of blast-induced injury in the rat auditory cortex |
title_full | Time course of blast-induced injury in the rat auditory cortex |
title_fullStr | Time course of blast-induced injury in the rat auditory cortex |
title_full_unstemmed | Time course of blast-induced injury in the rat auditory cortex |
title_short | Time course of blast-induced injury in the rat auditory cortex |
title_sort | time course of blast-induced injury in the rat auditory cortex |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831391/ https://www.ncbi.nlm.nih.gov/pubmed/29489862 http://dx.doi.org/10.1371/journal.pone.0193389 |
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