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The recovery of standing and locomotion after spinal cord injury does not require task-specific training
After complete spinal cord injury, mammals, including mice, rats and cats, recover hindlimb locomotion with treadmill training. The premise is that sensory cues consistent with locomotion reorganize spinal sensorimotor circuits. Here, we show that hindlimb standing and locomotion recover after spina...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924957/ https://www.ncbi.nlm.nih.gov/pubmed/31825306 http://dx.doi.org/10.7554/eLife.50134 |
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author | Harnie, Jonathan Doelman, Adam de Vette, Emmanuelle Audet, Johannie Desrochers, Etienne Gaudreault, Nathaly Frigon, Alain |
author_facet | Harnie, Jonathan Doelman, Adam de Vette, Emmanuelle Audet, Johannie Desrochers, Etienne Gaudreault, Nathaly Frigon, Alain |
author_sort | Harnie, Jonathan |
collection | PubMed |
description | After complete spinal cord injury, mammals, including mice, rats and cats, recover hindlimb locomotion with treadmill training. The premise is that sensory cues consistent with locomotion reorganize spinal sensorimotor circuits. Here, we show that hindlimb standing and locomotion recover after spinal transection in cats without task-specific training. Spinal-transected cats recovered full weight bearing standing and locomotion after five weeks of rhythmic manual stimulation of triceps surae muscles (non-specific training) and without any intervention. Moreover, cats modulated locomotor speed and performed split-belt locomotion six weeks after spinal transection, functions that were not trained or tested in the weeks prior. This indicates that spinal networks controlling standing and locomotion and their interactions with sensory feedback from the limbs remain largely intact after complete spinal cord injury. We conclude that standing and locomotor recovery is due to the return of neuronal excitability within spinal sensorimotor circuits that do not require task-specific activity-dependent plasticity. |
format | Online Article Text |
id | pubmed-6924957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69249572019-12-23 The recovery of standing and locomotion after spinal cord injury does not require task-specific training Harnie, Jonathan Doelman, Adam de Vette, Emmanuelle Audet, Johannie Desrochers, Etienne Gaudreault, Nathaly Frigon, Alain eLife Neuroscience After complete spinal cord injury, mammals, including mice, rats and cats, recover hindlimb locomotion with treadmill training. The premise is that sensory cues consistent with locomotion reorganize spinal sensorimotor circuits. Here, we show that hindlimb standing and locomotion recover after spinal transection in cats without task-specific training. Spinal-transected cats recovered full weight bearing standing and locomotion after five weeks of rhythmic manual stimulation of triceps surae muscles (non-specific training) and without any intervention. Moreover, cats modulated locomotor speed and performed split-belt locomotion six weeks after spinal transection, functions that were not trained or tested in the weeks prior. This indicates that spinal networks controlling standing and locomotion and their interactions with sensory feedback from the limbs remain largely intact after complete spinal cord injury. We conclude that standing and locomotor recovery is due to the return of neuronal excitability within spinal sensorimotor circuits that do not require task-specific activity-dependent plasticity. eLife Sciences Publications, Ltd 2019-12-11 /pmc/articles/PMC6924957/ /pubmed/31825306 http://dx.doi.org/10.7554/eLife.50134 Text en © 2019, Harnie et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Harnie, Jonathan Doelman, Adam de Vette, Emmanuelle Audet, Johannie Desrochers, Etienne Gaudreault, Nathaly Frigon, Alain The recovery of standing and locomotion after spinal cord injury does not require task-specific training |
title | The recovery of standing and locomotion after spinal cord injury does not require task-specific training |
title_full | The recovery of standing and locomotion after spinal cord injury does not require task-specific training |
title_fullStr | The recovery of standing and locomotion after spinal cord injury does not require task-specific training |
title_full_unstemmed | The recovery of standing and locomotion after spinal cord injury does not require task-specific training |
title_short | The recovery of standing and locomotion after spinal cord injury does not require task-specific training |
title_sort | recovery of standing and locomotion after spinal cord injury does not require task-specific training |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924957/ https://www.ncbi.nlm.nih.gov/pubmed/31825306 http://dx.doi.org/10.7554/eLife.50134 |
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