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Laterality and region-specific tau phosphorylation correlate with PTSD-related behavioral traits in rats exposed to repetitive low-level blast
Military veterans who experience blast-related traumatic brain injuries often suffer from chronic cognitive and neurobehavioral syndromes. Reports of abnormal tau processing following blast injury have raised concerns that some cases may have a neurodegenerative basis. Rats exposed to repetitive low...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923605/ https://www.ncbi.nlm.nih.gov/pubmed/33648608 http://dx.doi.org/10.1186/s40478-021-01128-3 |
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author | Perez Garcia, Georgina De Gasperi, Rita Gama Sosa, Miguel A. Perez, Gissel M. Otero-Pagan, Alena Pryor, Dylan Abutarboush, Rania Kawoos, Usmah Hof, Patrick R. Dickstein, Dara L. Cook, David G. Gandy, Sam Ahlers, Stephen T. Elder, Gregory A. |
author_facet | Perez Garcia, Georgina De Gasperi, Rita Gama Sosa, Miguel A. Perez, Gissel M. Otero-Pagan, Alena Pryor, Dylan Abutarboush, Rania Kawoos, Usmah Hof, Patrick R. Dickstein, Dara L. Cook, David G. Gandy, Sam Ahlers, Stephen T. Elder, Gregory A. |
author_sort | Perez Garcia, Georgina |
collection | PubMed |
description | Military veterans who experience blast-related traumatic brain injuries often suffer from chronic cognitive and neurobehavioral syndromes. Reports of abnormal tau processing following blast injury have raised concerns that some cases may have a neurodegenerative basis. Rats exposed to repetitive low-level blast exhibit chronic neurobehavioral traits and accumulate tau phosphorylated at threonine 181 (Thr181). Using data previously reported in separate studies we tested the hypothesis that region-specific patterns of Thr181 phosphorylation correlate with behavioral measures also previously determined and reported in the same animals. Elevated p-tau Thr181 in anterior neocortical regions and right hippocampus correlated with anxiety as well as fear learning and novel object localization. There were no correlations with levels in amygdala or posterior neocortical regions. Particularly striking were asymmetrical effects on the right and left hippocampus. No systematic variation in head orientation toward the blast wave seems to explain the laterality. Levels did not correlate with behavioral measures of hyperarousal. Results were specific to Thr181 in that no correlations were observed for three other phospho-acceptor sites (threonine 231, serine 396, and serine 404). No consistent correlations were linked with total tau. These correlations are significant in suggesting that p-tau accumulation in anterior neocortical regions and the hippocampus may lead to disinhibited amygdala function without p-tau elevation in the amygdala itself. They also suggest an association linking blast injury with tauopathy, which has implications for understanding the relationship of chronic blast-related neurobehavioral syndromes in humans to neurodegenerative diseases. |
format | Online Article Text |
id | pubmed-7923605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79236052021-03-02 Laterality and region-specific tau phosphorylation correlate with PTSD-related behavioral traits in rats exposed to repetitive low-level blast Perez Garcia, Georgina De Gasperi, Rita Gama Sosa, Miguel A. Perez, Gissel M. Otero-Pagan, Alena Pryor, Dylan Abutarboush, Rania Kawoos, Usmah Hof, Patrick R. Dickstein, Dara L. Cook, David G. Gandy, Sam Ahlers, Stephen T. Elder, Gregory A. Acta Neuropathol Commun Research Military veterans who experience blast-related traumatic brain injuries often suffer from chronic cognitive and neurobehavioral syndromes. Reports of abnormal tau processing following blast injury have raised concerns that some cases may have a neurodegenerative basis. Rats exposed to repetitive low-level blast exhibit chronic neurobehavioral traits and accumulate tau phosphorylated at threonine 181 (Thr181). Using data previously reported in separate studies we tested the hypothesis that region-specific patterns of Thr181 phosphorylation correlate with behavioral measures also previously determined and reported in the same animals. Elevated p-tau Thr181 in anterior neocortical regions and right hippocampus correlated with anxiety as well as fear learning and novel object localization. There were no correlations with levels in amygdala or posterior neocortical regions. Particularly striking were asymmetrical effects on the right and left hippocampus. No systematic variation in head orientation toward the blast wave seems to explain the laterality. Levels did not correlate with behavioral measures of hyperarousal. Results were specific to Thr181 in that no correlations were observed for three other phospho-acceptor sites (threonine 231, serine 396, and serine 404). No consistent correlations were linked with total tau. These correlations are significant in suggesting that p-tau accumulation in anterior neocortical regions and the hippocampus may lead to disinhibited amygdala function without p-tau elevation in the amygdala itself. They also suggest an association linking blast injury with tauopathy, which has implications for understanding the relationship of chronic blast-related neurobehavioral syndromes in humans to neurodegenerative diseases. BioMed Central 2021-03-01 /pmc/articles/PMC7923605/ /pubmed/33648608 http://dx.doi.org/10.1186/s40478-021-01128-3 Text en © The Author(s) 2021 Open AccessThis 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/. 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 in a credit line to the data. |
spellingShingle | Research Perez Garcia, Georgina De Gasperi, Rita Gama Sosa, Miguel A. Perez, Gissel M. Otero-Pagan, Alena Pryor, Dylan Abutarboush, Rania Kawoos, Usmah Hof, Patrick R. Dickstein, Dara L. Cook, David G. Gandy, Sam Ahlers, Stephen T. Elder, Gregory A. Laterality and region-specific tau phosphorylation correlate with PTSD-related behavioral traits in rats exposed to repetitive low-level blast |
title | Laterality and region-specific tau phosphorylation correlate with PTSD-related behavioral traits in rats exposed to repetitive low-level blast |
title_full | Laterality and region-specific tau phosphorylation correlate with PTSD-related behavioral traits in rats exposed to repetitive low-level blast |
title_fullStr | Laterality and region-specific tau phosphorylation correlate with PTSD-related behavioral traits in rats exposed to repetitive low-level blast |
title_full_unstemmed | Laterality and region-specific tau phosphorylation correlate with PTSD-related behavioral traits in rats exposed to repetitive low-level blast |
title_short | Laterality and region-specific tau phosphorylation correlate with PTSD-related behavioral traits in rats exposed to repetitive low-level blast |
title_sort | laterality and region-specific tau phosphorylation correlate with ptsd-related behavioral traits in rats exposed to repetitive low-level blast |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923605/ https://www.ncbi.nlm.nih.gov/pubmed/33648608 http://dx.doi.org/10.1186/s40478-021-01128-3 |
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