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Research ArticleNew Research, Disorders of the Nervous System

Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1G93A Rat Model

Gretchen M. Thomsen, Jean-Philippe Vit, Alexander Lamb, Genevieve Gowing, Oksana Shelest, Mor Alkaslasi, Eric J. Ley and Clive N. Svendsen
eNeuro 22 June 2015, 2 (3) ENEURO.0059-14.2015; https://doi.org/10.1523/ENEURO.0059-14.2015
Gretchen M. Thomsen
1 Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048
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Jean-Philippe Vit
2Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048
3 Biobehavioral Research Core, Cedars-Sinai Medical Center, Los Angeles, CA 90048
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Alexander Lamb
4Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA 90048
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Genevieve Gowing
1 Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048
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Oksana Shelest
1 Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048
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Mor Alkaslasi
1 Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048
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Eric J. Ley
4Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA 90048
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Clive N. Svendsen
1 Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048
2Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048
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Abstract

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.

  • ALS
  • amyotrophic lateral sclerosis
  • neurodegeneration
  • SOD1
  • TBI
  • traumatic brain injury

Footnotes

  • ↵1 The authors declare no competing financial interests.

  • ↵3 This work was supported by the Board of Governors Regenerative Medicine Institute and the ALS Association.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

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eneuro: 2 (3)
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May/June 2015
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Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1G93A Rat Model
Gretchen M. Thomsen, Jean-Philippe Vit, Alexander Lamb, Genevieve Gowing, Oksana Shelest, Mor Alkaslasi, Eric J. Ley, Clive N. Svendsen
eNeuro 22 June 2015, 2 (3) ENEURO.0059-14.2015; DOI: 10.1523/ENEURO.0059-14.2015

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Acute Traumatic Brain Injury Does Not Exacerbate Amyotrophic Lateral Sclerosis in the SOD1G93A Rat Model
Gretchen M. Thomsen, Jean-Philippe Vit, Alexander Lamb, Genevieve Gowing, Oksana Shelest, Mor Alkaslasi, Eric J. Ley, Clive N. Svendsen
eNeuro 22 June 2015, 2 (3) ENEURO.0059-14.2015; DOI: 10.1523/ENEURO.0059-14.2015
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Keywords

  • ALS
  • amyotrophic lateral sclerosis
  • neurodegeneration
  • SOD1
  • TBI
  • traumatic brain injury

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