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Electrophysiological Correlates of Blast-Wave Induced Cerebellar Injury
Understanding the mechanisms underlying traumatic neural injury and the sequelae of events in the acute phase is important for deciding on the best window of therapeutic intervention. We hypothesized that evoked potentials (EP) recorded from the cerebellar cortex can detect mild levels of neural tra...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134123/ https://www.ncbi.nlm.nih.gov/pubmed/30206255 http://dx.doi.org/10.1038/s41598-018-31728-4 |
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author | Ordek, Gokhan Asan, Ahmet S. Cetinkaya, Esma Skotak, Maciej Kakulavarapu, Venkata R. Chandra, Namas Sahin, Mesut |
author_facet | Ordek, Gokhan Asan, Ahmet S. Cetinkaya, Esma Skotak, Maciej Kakulavarapu, Venkata R. Chandra, Namas Sahin, Mesut |
author_sort | Ordek, Gokhan |
collection | PubMed |
description | Understanding the mechanisms underlying traumatic neural injury and the sequelae of events in the acute phase is important for deciding on the best window of therapeutic intervention. We hypothesized that evoked potentials (EP) recorded from the cerebellar cortex can detect mild levels of neural trauma and provide a qualitative assessment tool for progression of cerebellar injury in time. The cerebellar local field potentials evoked by a mechanical tap on the hand and collected with chronically implanted micro-ECoG arrays on the rat cerebellar cortex demonstrated substantial changes both in amplitude and timing as a result of blast-wave induced injury. The results revealed that the largest EP changes occurred within the first day of injury, and partial recoveries were observed from day-1 to day-3, followed by a period of gradual improvements (day-7 to day-14). The mossy fiber (MF) and climbing fiber (CF) mediated components of the EPs were affected differentially. The behavioral tests (ladder rung walking) and immunohistological analysis (calbindin and caspase-3) did not reveal any detectable changes at these blast pressures that are typically considered as mild (100–130 kPa). The results demonstrate the sensitivity of the electrophysiological method and its use as a tool to monitor the progression of cerebellar injuries in longitudinal animal studies. |
format | Online Article Text |
id | pubmed-6134123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61341232018-09-15 Electrophysiological Correlates of Blast-Wave Induced Cerebellar Injury Ordek, Gokhan Asan, Ahmet S. Cetinkaya, Esma Skotak, Maciej Kakulavarapu, Venkata R. Chandra, Namas Sahin, Mesut Sci Rep Article Understanding the mechanisms underlying traumatic neural injury and the sequelae of events in the acute phase is important for deciding on the best window of therapeutic intervention. We hypothesized that evoked potentials (EP) recorded from the cerebellar cortex can detect mild levels of neural trauma and provide a qualitative assessment tool for progression of cerebellar injury in time. The cerebellar local field potentials evoked by a mechanical tap on the hand and collected with chronically implanted micro-ECoG arrays on the rat cerebellar cortex demonstrated substantial changes both in amplitude and timing as a result of blast-wave induced injury. The results revealed that the largest EP changes occurred within the first day of injury, and partial recoveries were observed from day-1 to day-3, followed by a period of gradual improvements (day-7 to day-14). The mossy fiber (MF) and climbing fiber (CF) mediated components of the EPs were affected differentially. The behavioral tests (ladder rung walking) and immunohistological analysis (calbindin and caspase-3) did not reveal any detectable changes at these blast pressures that are typically considered as mild (100–130 kPa). The results demonstrate the sensitivity of the electrophysiological method and its use as a tool to monitor the progression of cerebellar injuries in longitudinal animal studies. Nature Publishing Group UK 2018-09-11 /pmc/articles/PMC6134123/ /pubmed/30206255 http://dx.doi.org/10.1038/s41598-018-31728-4 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ordek, Gokhan Asan, Ahmet S. Cetinkaya, Esma Skotak, Maciej Kakulavarapu, Venkata R. Chandra, Namas Sahin, Mesut Electrophysiological Correlates of Blast-Wave Induced Cerebellar Injury |
title | Electrophysiological Correlates of Blast-Wave Induced Cerebellar Injury |
title_full | Electrophysiological Correlates of Blast-Wave Induced Cerebellar Injury |
title_fullStr | Electrophysiological Correlates of Blast-Wave Induced Cerebellar Injury |
title_full_unstemmed | Electrophysiological Correlates of Blast-Wave Induced Cerebellar Injury |
title_short | Electrophysiological Correlates of Blast-Wave Induced Cerebellar Injury |
title_sort | electrophysiological correlates of blast-wave induced cerebellar injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134123/ https://www.ncbi.nlm.nih.gov/pubmed/30206255 http://dx.doi.org/10.1038/s41598-018-31728-4 |
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