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Electrical spinal cord stimulation must preserve proprioception to enable locomotion in humans with spinal cord injury
Epidural electrical stimulation (EES) of the spinal cord restores locomotion in animal models of spinal cord injury (SCI) but is less effective in humans. Here, we hypothesized that this inter-species discrepancy is due to interference between EES and proprioceptive information in humans. Computatio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268129/ https://www.ncbi.nlm.nih.gov/pubmed/30382196 http://dx.doi.org/10.1038/s41593-018-0262-6 |
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author | Formento, E. Minassian, K. Wagner, F. Mignardot, JB. Le Goff, C. G. Rowald, A. Bloch, J. Micera, S. Capogrosso, M. Courtine, G. |
author_facet | Formento, E. Minassian, K. Wagner, F. Mignardot, JB. Le Goff, C. G. Rowald, A. Bloch, J. Micera, S. Capogrosso, M. Courtine, G. |
author_sort | Formento, E. |
collection | PubMed |
description | Epidural electrical stimulation (EES) of the spinal cord restores locomotion in animal models of spinal cord injury (SCI) but is less effective in humans. Here, we hypothesized that this inter-species discrepancy is due to interference between EES and proprioceptive information in humans. Computational simulations, preclinical and clinical experiments reveal that EES blocks a significant amount of proprioceptive input in humans, but not in rats. This transient deafferentation prevents the modulation of reciprocal inhibitory networks involved in locomotion and reduces or abolishes the conscious perception of leg position. Consequently, continuous EES can only facilitate locomotion within a narrow range of stimulation parameters and is unable to provide meaningful locomotor improvements in humans without rehabilitation. Simulations showed that burst stimulation and spatiotemporal stimulation profiles mitigate the cancellation of proprioceptive information, enabling robust control over motoneuron activity. This demonstrates the importance of stimulation protocols that preserve proprioceptive information to facilitate walking with EES. |
format | Online Article Text |
id | pubmed-6268129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-62681292019-04-30 Electrical spinal cord stimulation must preserve proprioception to enable locomotion in humans with spinal cord injury Formento, E. Minassian, K. Wagner, F. Mignardot, JB. Le Goff, C. G. Rowald, A. Bloch, J. Micera, S. Capogrosso, M. Courtine, G. Nat Neurosci Article Epidural electrical stimulation (EES) of the spinal cord restores locomotion in animal models of spinal cord injury (SCI) but is less effective in humans. Here, we hypothesized that this inter-species discrepancy is due to interference between EES and proprioceptive information in humans. Computational simulations, preclinical and clinical experiments reveal that EES blocks a significant amount of proprioceptive input in humans, but not in rats. This transient deafferentation prevents the modulation of reciprocal inhibitory networks involved in locomotion and reduces or abolishes the conscious perception of leg position. Consequently, continuous EES can only facilitate locomotion within a narrow range of stimulation parameters and is unable to provide meaningful locomotor improvements in humans without rehabilitation. Simulations showed that burst stimulation and spatiotemporal stimulation profiles mitigate the cancellation of proprioceptive information, enabling robust control over motoneuron activity. This demonstrates the importance of stimulation protocols that preserve proprioceptive information to facilitate walking with EES. 2018-10-31 2018-12 /pmc/articles/PMC6268129/ /pubmed/30382196 http://dx.doi.org/10.1038/s41593-018-0262-6 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Formento, E. Minassian, K. Wagner, F. Mignardot, JB. Le Goff, C. G. Rowald, A. Bloch, J. Micera, S. Capogrosso, M. Courtine, G. Electrical spinal cord stimulation must preserve proprioception to enable locomotion in humans with spinal cord injury |
title | Electrical spinal cord stimulation must preserve proprioception to
enable locomotion in humans with spinal cord injury |
title_full | Electrical spinal cord stimulation must preserve proprioception to
enable locomotion in humans with spinal cord injury |
title_fullStr | Electrical spinal cord stimulation must preserve proprioception to
enable locomotion in humans with spinal cord injury |
title_full_unstemmed | Electrical spinal cord stimulation must preserve proprioception to
enable locomotion in humans with spinal cord injury |
title_short | Electrical spinal cord stimulation must preserve proprioception to
enable locomotion in humans with spinal cord injury |
title_sort | electrical spinal cord stimulation must preserve proprioception to
enable locomotion in humans with spinal cord injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268129/ https://www.ncbi.nlm.nih.gov/pubmed/30382196 http://dx.doi.org/10.1038/s41593-018-0262-6 |
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