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Pathological Changes in the White Matter after Spinal Contusion Injury in the Rat
It has been shown previously that after spinal cord injury, the loss of grey matter is relatively faster than loss of white matter suggesting interventions to save white matter tracts offer better therapeutic possibilities. Loss of white matter in and around the injury site is believed to be the mai...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430695/ https://www.ncbi.nlm.nih.gov/pubmed/22952690 http://dx.doi.org/10.1371/journal.pone.0043484 |
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author | Ek, C. Joakim Habgood, Mark D. Dennis, Ross Dziegielewska, Katarzyna M. Mallard, Carina Wheaton, Benjamin Saunders, Norman R. |
author_facet | Ek, C. Joakim Habgood, Mark D. Dennis, Ross Dziegielewska, Katarzyna M. Mallard, Carina Wheaton, Benjamin Saunders, Norman R. |
author_sort | Ek, C. Joakim |
collection | PubMed |
description | It has been shown previously that after spinal cord injury, the loss of grey matter is relatively faster than loss of white matter suggesting interventions to save white matter tracts offer better therapeutic possibilities. Loss of white matter in and around the injury site is believed to be the main underlying cause for the subsequent loss of neurological functions. In this study we used a series of techniques, including estimations of the number of axons with pathology, immunohistochemistry and mapping of distribution of pathological axons, to better understand the temporal and spatial pathological events in white matter following contusion injury to the rat spinal cord. There was an initial rapid loss of axons with no detectable further loss beyond 1 week after injury. Immunoreactivity for CNPase indicated that changes to oligodendrocytes are rapid, extending to several millimetres away from injury site and preceding much of the axonal loss, giving early prediction of the final volume of white matter that survived. It seems that in juvenile rats the myelination of axons in white matter tracts continues for some time, which has an important bearing on interpretation of our, and previous, studies. The amount of myelin debris and axon pathology progressively decreased with time but could still be observed at 10 weeks after injury, especially at more distant rostral and caudal levels from the injury site. This study provides new methods to assess injuries to spinal cord and indicates that early interventions are needed for the successful sparing of white matter tracts following injury. |
format | Online Article Text |
id | pubmed-3430695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34306952012-09-05 Pathological Changes in the White Matter after Spinal Contusion Injury in the Rat Ek, C. Joakim Habgood, Mark D. Dennis, Ross Dziegielewska, Katarzyna M. Mallard, Carina Wheaton, Benjamin Saunders, Norman R. PLoS One Research Article It has been shown previously that after spinal cord injury, the loss of grey matter is relatively faster than loss of white matter suggesting interventions to save white matter tracts offer better therapeutic possibilities. Loss of white matter in and around the injury site is believed to be the main underlying cause for the subsequent loss of neurological functions. In this study we used a series of techniques, including estimations of the number of axons with pathology, immunohistochemistry and mapping of distribution of pathological axons, to better understand the temporal and spatial pathological events in white matter following contusion injury to the rat spinal cord. There was an initial rapid loss of axons with no detectable further loss beyond 1 week after injury. Immunoreactivity for CNPase indicated that changes to oligodendrocytes are rapid, extending to several millimetres away from injury site and preceding much of the axonal loss, giving early prediction of the final volume of white matter that survived. It seems that in juvenile rats the myelination of axons in white matter tracts continues for some time, which has an important bearing on interpretation of our, and previous, studies. The amount of myelin debris and axon pathology progressively decreased with time but could still be observed at 10 weeks after injury, especially at more distant rostral and caudal levels from the injury site. This study provides new methods to assess injuries to spinal cord and indicates that early interventions are needed for the successful sparing of white matter tracts following injury. Public Library of Science 2012-08-29 /pmc/articles/PMC3430695/ /pubmed/22952690 http://dx.doi.org/10.1371/journal.pone.0043484 Text en © 2012 Ek et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ek, C. Joakim Habgood, Mark D. Dennis, Ross Dziegielewska, Katarzyna M. Mallard, Carina Wheaton, Benjamin Saunders, Norman R. Pathological Changes in the White Matter after Spinal Contusion Injury in the Rat |
title | Pathological Changes in the White Matter after Spinal Contusion Injury in the Rat |
title_full | Pathological Changes in the White Matter after Spinal Contusion Injury in the Rat |
title_fullStr | Pathological Changes in the White Matter after Spinal Contusion Injury in the Rat |
title_full_unstemmed | Pathological Changes in the White Matter after Spinal Contusion Injury in the Rat |
title_short | Pathological Changes in the White Matter after Spinal Contusion Injury in the Rat |
title_sort | pathological changes in the white matter after spinal contusion injury in the rat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430695/ https://www.ncbi.nlm.nih.gov/pubmed/22952690 http://dx.doi.org/10.1371/journal.pone.0043484 |
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