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Aberrant Crossed Corticospinal Facilitation in Muscles Distant from a Spinal Cord Injury
Crossed facilitatory interactions in the corticospinal pathway are impaired in humans with chronic incomplete spinal cord injury (SCI). The extent to which crossed facilitation is affected in muscles above and below the injury remains unknown. To address this question we tested 51 patients with neur...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798423/ https://www.ncbi.nlm.nih.gov/pubmed/24146921 http://dx.doi.org/10.1371/journal.pone.0076747 |
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author | Bunday, Karen L. Oudega, Martin Perez, Monica A. |
author_facet | Bunday, Karen L. Oudega, Martin Perez, Monica A. |
author_sort | Bunday, Karen L. |
collection | PubMed |
description | Crossed facilitatory interactions in the corticospinal pathway are impaired in humans with chronic incomplete spinal cord injury (SCI). The extent to which crossed facilitation is affected in muscles above and below the injury remains unknown. To address this question we tested 51 patients with neurological injuries between C2-T12 and 17 age-matched healthy controls. Using transcranial magnetic stimulation we elicited motor evoked potentials (MEPs) in the resting first dorsal interosseous, biceps brachii, and tibialis anterior muscles when the contralateral side remained at rest or performed 70% of maximal voluntary contraction (MVC) into index finger abduction, elbow flexion, and ankle dorsiflexion, respectively. By testing MEPs in muscles with motoneurons located at different spinal cord segments we were able to relate the neurological level of injury to be above, at, or below the location of the motoneurons of the muscle tested. We demonstrate that in patients the size of MEPs was increased to a similar extent as in controls in muscles above the injury during 70% of MVC compared to rest. MEPs remained unchanged in muscles at and within 5 segments below the injury during 70% of MVC compared to rest. However, in muscles beyond 5 segments below the injury the size of MEPs increased similar to controls and was aberrantly high, 2-fold above controls, in muscles distant (>15 segments) from the injury. These aberrantly large MEPs were accompanied by larger F-wave amplitudes compared to controls. Thus, our findings support the view that corticospinal degeneration does not spread rostral to the lesion, and highlights the potential of caudal regions distant from an injury to facilitate residual corticospinal output after SCI. |
format | Online Article Text |
id | pubmed-3798423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37984232013-10-21 Aberrant Crossed Corticospinal Facilitation in Muscles Distant from a Spinal Cord Injury Bunday, Karen L. Oudega, Martin Perez, Monica A. PLoS One Research Article Crossed facilitatory interactions in the corticospinal pathway are impaired in humans with chronic incomplete spinal cord injury (SCI). The extent to which crossed facilitation is affected in muscles above and below the injury remains unknown. To address this question we tested 51 patients with neurological injuries between C2-T12 and 17 age-matched healthy controls. Using transcranial magnetic stimulation we elicited motor evoked potentials (MEPs) in the resting first dorsal interosseous, biceps brachii, and tibialis anterior muscles when the contralateral side remained at rest or performed 70% of maximal voluntary contraction (MVC) into index finger abduction, elbow flexion, and ankle dorsiflexion, respectively. By testing MEPs in muscles with motoneurons located at different spinal cord segments we were able to relate the neurological level of injury to be above, at, or below the location of the motoneurons of the muscle tested. We demonstrate that in patients the size of MEPs was increased to a similar extent as in controls in muscles above the injury during 70% of MVC compared to rest. MEPs remained unchanged in muscles at and within 5 segments below the injury during 70% of MVC compared to rest. However, in muscles beyond 5 segments below the injury the size of MEPs increased similar to controls and was aberrantly high, 2-fold above controls, in muscles distant (>15 segments) from the injury. These aberrantly large MEPs were accompanied by larger F-wave amplitudes compared to controls. Thus, our findings support the view that corticospinal degeneration does not spread rostral to the lesion, and highlights the potential of caudal regions distant from an injury to facilitate residual corticospinal output after SCI. Public Library of Science 2013-10-17 /pmc/articles/PMC3798423/ /pubmed/24146921 http://dx.doi.org/10.1371/journal.pone.0076747 Text en © 2013 Bunday 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 Bunday, Karen L. Oudega, Martin Perez, Monica A. Aberrant Crossed Corticospinal Facilitation in Muscles Distant from a Spinal Cord Injury |
title | Aberrant Crossed Corticospinal Facilitation in Muscles Distant from a Spinal Cord Injury |
title_full | Aberrant Crossed Corticospinal Facilitation in Muscles Distant from a Spinal Cord Injury |
title_fullStr | Aberrant Crossed Corticospinal Facilitation in Muscles Distant from a Spinal Cord Injury |
title_full_unstemmed | Aberrant Crossed Corticospinal Facilitation in Muscles Distant from a Spinal Cord Injury |
title_short | Aberrant Crossed Corticospinal Facilitation in Muscles Distant from a Spinal Cord Injury |
title_sort | aberrant crossed corticospinal facilitation in muscles distant from a spinal cord injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798423/ https://www.ncbi.nlm.nih.gov/pubmed/24146921 http://dx.doi.org/10.1371/journal.pone.0076747 |
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