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A novel simple traumatic brain injury mouse model
BACKGROUND: Traumatic brain injury, one of the leading causes of death in adults under 40 years of age in the world, is frequently caused by mechanical shock, resulting in diffuse neuronal damage and long-term cognitive dysfunction. Many existing TBI animal models revival with expensive equipment or...
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/PMC8974042/ https://www.ncbi.nlm.nih.gov/pubmed/35361274 http://dx.doi.org/10.1186/s41016-022-00273-5 |
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author | Chen, Chen Hou, Jiawei Lu, Junfeng Zhu, Zeyu Yang, Yang Peng, Weijia Pi, Rongbiao |
author_facet | Chen, Chen Hou, Jiawei Lu, Junfeng Zhu, Zeyu Yang, Yang Peng, Weijia Pi, Rongbiao |
author_sort | Chen, Chen |
collection | PubMed |
description | BACKGROUND: Traumatic brain injury, one of the leading causes of death in adults under 40 years of age in the world, is frequently caused by mechanical shock, resulting in diffuse neuronal damage and long-term cognitive dysfunction. Many existing TBI animal models revival with expensive equipment or special room are needed or the processes of operations are complex and not easy to be widely used. Therefore, a simpler TBI model needs to be designed. METHODS: Our TBI model is an innovation of the modeling method through air guns shutting rubber bullets. A core facet is the application of our designed rubber bullet impact device. It could focus the hitting power to the fixed site of the brain, thus triggering a mild closed head injury. Moreover, the degree of damage can be adjusted by the times of shots. RESULTS: Our model induced blood-brain barrier leakage and diffused neuronal damage. Besides, it led to an increased level of Tau phosphorylation and resulted in cognitive dysfunction within several weeks post-injury. CONCLUSION: Our TBI model is not only simple and time-saving but also can simulate mild brain injuries in clinical. It is suitable for exploring pathobiological mechanisms as well as a screening of potential therapies for TBI. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41016-022-00273-5. |
format | Online Article Text |
id | pubmed-8974042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89740422022-04-02 A novel simple traumatic brain injury mouse model Chen, Chen Hou, Jiawei Lu, Junfeng Zhu, Zeyu Yang, Yang Peng, Weijia Pi, Rongbiao Chin Neurosurg J Research BACKGROUND: Traumatic brain injury, one of the leading causes of death in adults under 40 years of age in the world, is frequently caused by mechanical shock, resulting in diffuse neuronal damage and long-term cognitive dysfunction. Many existing TBI animal models revival with expensive equipment or special room are needed or the processes of operations are complex and not easy to be widely used. Therefore, a simpler TBI model needs to be designed. METHODS: Our TBI model is an innovation of the modeling method through air guns shutting rubber bullets. A core facet is the application of our designed rubber bullet impact device. It could focus the hitting power to the fixed site of the brain, thus triggering a mild closed head injury. Moreover, the degree of damage can be adjusted by the times of shots. RESULTS: Our model induced blood-brain barrier leakage and diffused neuronal damage. Besides, it led to an increased level of Tau phosphorylation and resulted in cognitive dysfunction within several weeks post-injury. CONCLUSION: Our TBI model is not only simple and time-saving but also can simulate mild brain injuries in clinical. It is suitable for exploring pathobiological mechanisms as well as a screening of potential therapies for TBI. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41016-022-00273-5. BioMed Central 2022-04-01 /pmc/articles/PMC8974042/ /pubmed/35361274 http://dx.doi.org/10.1186/s41016-022-00273-5 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 Chen, Chen Hou, Jiawei Lu, Junfeng Zhu, Zeyu Yang, Yang Peng, Weijia Pi, Rongbiao A novel simple traumatic brain injury mouse model |
title | A novel simple traumatic brain injury mouse model |
title_full | A novel simple traumatic brain injury mouse model |
title_fullStr | A novel simple traumatic brain injury mouse model |
title_full_unstemmed | A novel simple traumatic brain injury mouse model |
title_short | A novel simple traumatic brain injury mouse model |
title_sort | novel simple traumatic brain injury mouse model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974042/ https://www.ncbi.nlm.nih.gov/pubmed/35361274 http://dx.doi.org/10.1186/s41016-022-00273-5 |
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