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The Involvement of Secondary Neuronal Damage in the Development of Neuropsychiatric Disorders Following Brain Insults
Neuropsychiatric disorders are one of the leading causes of disability worldwide and affect the health of billions of people. Previous publications have demonstrated that neuropsychiatric disorders can cause histomorphological damage in particular regions of the brain. By using a clinical symptom-co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949352/ https://www.ncbi.nlm.nih.gov/pubmed/24653712 http://dx.doi.org/10.3389/fneur.2014.00022 |
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author | Chen, Yun Garcia, Gregory E. Huang, Wei Constantini, Shlomi |
author_facet | Chen, Yun Garcia, Gregory E. Huang, Wei Constantini, Shlomi |
author_sort | Chen, Yun |
collection | PubMed |
description | Neuropsychiatric disorders are one of the leading causes of disability worldwide and affect the health of billions of people. Previous publications have demonstrated that neuropsychiatric disorders can cause histomorphological damage in particular regions of the brain. By using a clinical symptom-comparing approach, 55 neuropsychiatric signs or symptoms related usually to 14 types of acute and chronic brain insults were identified and categorized in the present study. Forty percent of the 55 neuropsychiatric signs and symptoms have been found to be commonly shared by the 14 brain insults. A meta-analysis supports existence of the same neuropsychiatric signs or symptoms in all brain insults. The results suggest that neuronal damage might be occurring in the same or similar regions or structures of the brain. Neuronal cell death, neural loss, and axonal degeneration in some parts of the brain (the limbic system, basal ganglia system, brainstem, cerebellum, and cerebral cortex) might be the histomorphological basis that is responsible for the neuropsychiatric symptom clusters. These morphological alterations may be the result of secondary neuronal damage (a cascade of progressive neural injury and neuronal cell death that is triggered by the initial insult). Secondary neuronal damage causes neuronal cell death and neural injury in not only the initial injured site but also remote brain regions. It may be a major contributor to subsequent neuropsychiatric disorders following brain insults. |
format | Online Article Text |
id | pubmed-3949352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39493522014-03-20 The Involvement of Secondary Neuronal Damage in the Development of Neuropsychiatric Disorders Following Brain Insults Chen, Yun Garcia, Gregory E. Huang, Wei Constantini, Shlomi Front Neurol Neuroscience Neuropsychiatric disorders are one of the leading causes of disability worldwide and affect the health of billions of people. Previous publications have demonstrated that neuropsychiatric disorders can cause histomorphological damage in particular regions of the brain. By using a clinical symptom-comparing approach, 55 neuropsychiatric signs or symptoms related usually to 14 types of acute and chronic brain insults were identified and categorized in the present study. Forty percent of the 55 neuropsychiatric signs and symptoms have been found to be commonly shared by the 14 brain insults. A meta-analysis supports existence of the same neuropsychiatric signs or symptoms in all brain insults. The results suggest that neuronal damage might be occurring in the same or similar regions or structures of the brain. Neuronal cell death, neural loss, and axonal degeneration in some parts of the brain (the limbic system, basal ganglia system, brainstem, cerebellum, and cerebral cortex) might be the histomorphological basis that is responsible for the neuropsychiatric symptom clusters. These morphological alterations may be the result of secondary neuronal damage (a cascade of progressive neural injury and neuronal cell death that is triggered by the initial insult). Secondary neuronal damage causes neuronal cell death and neural injury in not only the initial injured site but also remote brain regions. It may be a major contributor to subsequent neuropsychiatric disorders following brain insults. Frontiers Media S.A. 2014-03-11 /pmc/articles/PMC3949352/ /pubmed/24653712 http://dx.doi.org/10.3389/fneur.2014.00022 Text en Copyright © 2014 Chen, Garcia, Huang and Constantini. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Chen, Yun Garcia, Gregory E. Huang, Wei Constantini, Shlomi The Involvement of Secondary Neuronal Damage in the Development of Neuropsychiatric Disorders Following Brain Insults |
title | The Involvement of Secondary Neuronal Damage in the Development of Neuropsychiatric Disorders Following Brain Insults |
title_full | The Involvement of Secondary Neuronal Damage in the Development of Neuropsychiatric Disorders Following Brain Insults |
title_fullStr | The Involvement of Secondary Neuronal Damage in the Development of Neuropsychiatric Disorders Following Brain Insults |
title_full_unstemmed | The Involvement of Secondary Neuronal Damage in the Development of Neuropsychiatric Disorders Following Brain Insults |
title_short | The Involvement of Secondary Neuronal Damage in the Development of Neuropsychiatric Disorders Following Brain Insults |
title_sort | involvement of secondary neuronal damage in the development of neuropsychiatric disorders following brain insults |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949352/ https://www.ncbi.nlm.nih.gov/pubmed/24653712 http://dx.doi.org/10.3389/fneur.2014.00022 |
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