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Persistent white matter vulnerability in a mouse model of mild traumatic brain injury
BACKGROUND: Following one mild traumatic brain injury (mTBI), there is a window of vulnerability during which subsequent mTBIs can cause substantially exacerbated impairments. Currently, there are no known methods to monitor, shorten or mitigate this window. METHODS: To characterize a preclinical mo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290236/ https://www.ncbi.nlm.nih.gov/pubmed/35850624 http://dx.doi.org/10.1186/s12868-022-00730-y |
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author | Velayudhan, Prashanth S. Mak, Jordan J. Gazdzinski, Lisa M. Wheeler, Anne L. |
author_facet | Velayudhan, Prashanth S. Mak, Jordan J. Gazdzinski, Lisa M. Wheeler, Anne L. |
author_sort | Velayudhan, Prashanth S. |
collection | PubMed |
description | BACKGROUND: Following one mild traumatic brain injury (mTBI), there is a window of vulnerability during which subsequent mTBIs can cause substantially exacerbated impairments. Currently, there are no known methods to monitor, shorten or mitigate this window. METHODS: To characterize a preclinical model of this window of vulnerability, we first gave male and female mice one or two high-depth or low-depth mTBIs separated by 1, 7, or 14 days. We assessed brain white matter integrity using silver staining within the corpus callosum and optic tracts, as well as behavioural performance on the Y-maze test and visual cliff test. RESULTS: The injuries resulted in windows of white matter vulnerability longer than 2 weeks but produced no behavioural impairments. Notably, this window duration is substantially longer than those reported in any previous preclinical vulnerability study, despite our injury model likely being milder than the ones used in those studies. We also found that sex and impact depth differentially influenced white matter integrity in different white matter regions. CONCLUSIONS: These results suggest that the experimental window of vulnerability following mTBI may be longer than previously reported. Additionally, this work highlights the value of including white matter damage, sex, and replicable injury models for the study of post-mTBI vulnerability and establishes important groundwork for the investigation of potential vulnerability mechanisms, biomarkers, and therapies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12868-022-00730-y. |
format | Online Article Text |
id | pubmed-9290236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92902362022-07-19 Persistent white matter vulnerability in a mouse model of mild traumatic brain injury Velayudhan, Prashanth S. Mak, Jordan J. Gazdzinski, Lisa M. Wheeler, Anne L. BMC Neurosci Research Article BACKGROUND: Following one mild traumatic brain injury (mTBI), there is a window of vulnerability during which subsequent mTBIs can cause substantially exacerbated impairments. Currently, there are no known methods to monitor, shorten or mitigate this window. METHODS: To characterize a preclinical model of this window of vulnerability, we first gave male and female mice one or two high-depth or low-depth mTBIs separated by 1, 7, or 14 days. We assessed brain white matter integrity using silver staining within the corpus callosum and optic tracts, as well as behavioural performance on the Y-maze test and visual cliff test. RESULTS: The injuries resulted in windows of white matter vulnerability longer than 2 weeks but produced no behavioural impairments. Notably, this window duration is substantially longer than those reported in any previous preclinical vulnerability study, despite our injury model likely being milder than the ones used in those studies. We also found that sex and impact depth differentially influenced white matter integrity in different white matter regions. CONCLUSIONS: These results suggest that the experimental window of vulnerability following mTBI may be longer than previously reported. Additionally, this work highlights the value of including white matter damage, sex, and replicable injury models for the study of post-mTBI vulnerability and establishes important groundwork for the investigation of potential vulnerability mechanisms, biomarkers, and therapies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12868-022-00730-y. BioMed Central 2022-07-18 /pmc/articles/PMC9290236/ /pubmed/35850624 http://dx.doi.org/10.1186/s12868-022-00730-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Article Velayudhan, Prashanth S. Mak, Jordan J. Gazdzinski, Lisa M. Wheeler, Anne L. Persistent white matter vulnerability in a mouse model of mild traumatic brain injury |
title | Persistent white matter vulnerability in a mouse model of mild traumatic brain injury |
title_full | Persistent white matter vulnerability in a mouse model of mild traumatic brain injury |
title_fullStr | Persistent white matter vulnerability in a mouse model of mild traumatic brain injury |
title_full_unstemmed | Persistent white matter vulnerability in a mouse model of mild traumatic brain injury |
title_short | Persistent white matter vulnerability in a mouse model of mild traumatic brain injury |
title_sort | persistent white matter vulnerability in a mouse model of mild traumatic brain injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290236/ https://www.ncbi.nlm.nih.gov/pubmed/35850624 http://dx.doi.org/10.1186/s12868-022-00730-y |
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