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Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1(G93A) Rat Model1,2,3
Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease in which upper and lower motor neurons degenerate, leading to muscle atrophy, paralysis, and death within 3 to 5 years of onset. While a small percentage of ALS cases are genetically linked, the majority are sporadic with unknown or...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Society for Neuroscience
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586929/ https://www.ncbi.nlm.nih.gov/pubmed/26464984 http://dx.doi.org/10.1523/ENEURO.0059-14.2015 |
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author | Thomsen, Gretchen M. Vit, Jean-Philippe Lamb, Alexander Gowing, Genevieve Shelest, Oksana Alkaslasi, Mor Ley, Eric J. Svendsen, Clive N. |
author_facet | Thomsen, Gretchen M. Vit, Jean-Philippe Lamb, Alexander Gowing, Genevieve Shelest, Oksana Alkaslasi, Mor Ley, Eric J. Svendsen, Clive N. |
author_sort | Thomsen, Gretchen M. |
collection | PubMed |
description | Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease in which upper and lower motor neurons degenerate, leading to muscle atrophy, paralysis, and death within 3 to 5 years of onset. While a small percentage of ALS cases are genetically linked, the majority are sporadic with unknown origin. Currently, etiological links are associated with disease onset without mechanistic understanding. Of all the putative risk factors, however, head trauma has emerged as a consistent candidate for initiating the molecular cascades of ALS. Here, we test the hypothesis that traumatic brain injury (TBI) in the SOD1 (G93A) transgenic rat model of ALS leads to early disease onset and shortened lifespan. We demonstrate, however, that a one-time acute focal injury caused by controlled cortical impact does not affect disease onset or survival. Establishing the negligible involvement of a single acute focal brain injury in an ALS rat model increases the current understanding of the disease. Critically, untangling a single focal TBI from multiple mild injuries provides a rationale for scientists and physicians to increase focus on repeat injuries to hopefully pinpoint a contributing cause of ALS. |
format | Online Article Text |
id | pubmed-4586929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-45869292015-10-13 Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1(G93A) Rat Model1,2,3 Thomsen, Gretchen M. Vit, Jean-Philippe Lamb, Alexander Gowing, Genevieve Shelest, Oksana Alkaslasi, Mor Ley, Eric J. Svendsen, Clive N. eNeuro New Research Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease in which upper and lower motor neurons degenerate, leading to muscle atrophy, paralysis, and death within 3 to 5 years of onset. While a small percentage of ALS cases are genetically linked, the majority are sporadic with unknown origin. Currently, etiological links are associated with disease onset without mechanistic understanding. Of all the putative risk factors, however, head trauma has emerged as a consistent candidate for initiating the molecular cascades of ALS. Here, we test the hypothesis that traumatic brain injury (TBI) in the SOD1 (G93A) transgenic rat model of ALS leads to early disease onset and shortened lifespan. We demonstrate, however, that a one-time acute focal injury caused by controlled cortical impact does not affect disease onset or survival. Establishing the negligible involvement of a single acute focal brain injury in an ALS rat model increases the current understanding of the disease. Critically, untangling a single focal TBI from multiple mild injuries provides a rationale for scientists and physicians to increase focus on repeat injuries to hopefully pinpoint a contributing cause of ALS. Society for Neuroscience 2015-07-03 /pmc/articles/PMC4586929/ /pubmed/26464984 http://dx.doi.org/10.1523/ENEURO.0059-14.2015 Text en Copyright © 2015 Thomsen et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | New Research Thomsen, Gretchen M. Vit, Jean-Philippe Lamb, Alexander Gowing, Genevieve Shelest, Oksana Alkaslasi, Mor Ley, Eric J. Svendsen, Clive N. Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1(G93A) Rat Model1,2,3 |
title | Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1(G93A) Rat Model1,2,3 |
title_full | Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1(G93A) Rat Model1,2,3 |
title_fullStr | Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1(G93A) Rat Model1,2,3 |
title_full_unstemmed | Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1(G93A) Rat Model1,2,3 |
title_short | Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1(G93A) Rat Model1,2,3 |
title_sort | acute traumatic brain injury does not exacerbate amyotrophic lateral sclerosis in the sod1(g93a) rat model1,2,3 |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586929/ https://www.ncbi.nlm.nih.gov/pubmed/26464984 http://dx.doi.org/10.1523/ENEURO.0059-14.2015 |
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