Cargando…
Voluntary Modulation of Evoked Responses Generated by Epidural and Transcutaneous Spinal Stimulation in Humans with Spinal Cord Injury
Transcutaneous (TSS) and epidural spinal stimulation (ESS) are electrophysiological techniques that have been used to investigate the interactions between exogenous electrical stimuli and spinal sensorimotor networks that integrate descending motor signals with afferent inputs from the periphery dur...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584516/ https://www.ncbi.nlm.nih.gov/pubmed/34768418 http://dx.doi.org/10.3390/jcm10214898 |
_version_ | 1784597468281831424 |
---|---|
author | Calvert, Jonathan S. Gill, Megan L. Linde, Margaux B. Veith, Daniel D. Thoreson, Andrew R. Lopez, Cesar Lee, Kendall H. Gerasimenko, Yury P. Edgerton, Victor R. Lavrov, Igor A. Zhao, Kristin D. Grahn, Peter J. Sayenko, Dimitry G. |
author_facet | Calvert, Jonathan S. Gill, Megan L. Linde, Margaux B. Veith, Daniel D. Thoreson, Andrew R. Lopez, Cesar Lee, Kendall H. Gerasimenko, Yury P. Edgerton, Victor R. Lavrov, Igor A. Zhao, Kristin D. Grahn, Peter J. Sayenko, Dimitry G. |
author_sort | Calvert, Jonathan S. |
collection | PubMed |
description | Transcutaneous (TSS) and epidural spinal stimulation (ESS) are electrophysiological techniques that have been used to investigate the interactions between exogenous electrical stimuli and spinal sensorimotor networks that integrate descending motor signals with afferent inputs from the periphery during motor tasks such as standing and stepping. Recently, pilot-phase clinical trials using ESS and TSS have demonstrated restoration of motor functions that were previously lost due to spinal cord injury (SCI). However, the spinal network interactions that occur in response to TSS or ESS pulses with spared descending connections across the site of SCI have yet to be characterized. Therefore, we examined the effects of delivering TSS or ESS pulses to the lumbosacral spinal cord in nine individuals with chronic SCI. During low-frequency stimulation, participants were instructed to relax or attempt maximum voluntary contraction to perform full leg flexion while supine. We observed similar lower-extremity neuromusculature activation during TSS and ESS when performed in the same participants while instructed to relax. Interestingly, when participants were instructed to attempt lower-extremity muscle contractions, both TSS- and ESS-evoked motor responses were significantly inhibited across all muscles. Participants with clinically complete SCI tested with ESS and participants with clinically incomplete SCI tested with TSS demonstrated greater ability to modulate evoked responses than participants with motor complete SCI tested with TSS, although this was not statistically significant due to a low number of subjects in each subgroup. These results suggest that descending commands combined with spinal stimulation may increase activity of inhibitory interneuronal circuitry within spinal sensorimotor networks in individuals with SCI, which may be relevant in the context of regaining functional motor outcomes. |
format | Online Article Text |
id | pubmed-8584516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85845162021-11-12 Voluntary Modulation of Evoked Responses Generated by Epidural and Transcutaneous Spinal Stimulation in Humans with Spinal Cord Injury Calvert, Jonathan S. Gill, Megan L. Linde, Margaux B. Veith, Daniel D. Thoreson, Andrew R. Lopez, Cesar Lee, Kendall H. Gerasimenko, Yury P. Edgerton, Victor R. Lavrov, Igor A. Zhao, Kristin D. Grahn, Peter J. Sayenko, Dimitry G. J Clin Med Article Transcutaneous (TSS) and epidural spinal stimulation (ESS) are electrophysiological techniques that have been used to investigate the interactions between exogenous electrical stimuli and spinal sensorimotor networks that integrate descending motor signals with afferent inputs from the periphery during motor tasks such as standing and stepping. Recently, pilot-phase clinical trials using ESS and TSS have demonstrated restoration of motor functions that were previously lost due to spinal cord injury (SCI). However, the spinal network interactions that occur in response to TSS or ESS pulses with spared descending connections across the site of SCI have yet to be characterized. Therefore, we examined the effects of delivering TSS or ESS pulses to the lumbosacral spinal cord in nine individuals with chronic SCI. During low-frequency stimulation, participants were instructed to relax or attempt maximum voluntary contraction to perform full leg flexion while supine. We observed similar lower-extremity neuromusculature activation during TSS and ESS when performed in the same participants while instructed to relax. Interestingly, when participants were instructed to attempt lower-extremity muscle contractions, both TSS- and ESS-evoked motor responses were significantly inhibited across all muscles. Participants with clinically complete SCI tested with ESS and participants with clinically incomplete SCI tested with TSS demonstrated greater ability to modulate evoked responses than participants with motor complete SCI tested with TSS, although this was not statistically significant due to a low number of subjects in each subgroup. These results suggest that descending commands combined with spinal stimulation may increase activity of inhibitory interneuronal circuitry within spinal sensorimotor networks in individuals with SCI, which may be relevant in the context of regaining functional motor outcomes. MDPI 2021-10-24 /pmc/articles/PMC8584516/ /pubmed/34768418 http://dx.doi.org/10.3390/jcm10214898 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Calvert, Jonathan S. Gill, Megan L. Linde, Margaux B. Veith, Daniel D. Thoreson, Andrew R. Lopez, Cesar Lee, Kendall H. Gerasimenko, Yury P. Edgerton, Victor R. Lavrov, Igor A. Zhao, Kristin D. Grahn, Peter J. Sayenko, Dimitry G. Voluntary Modulation of Evoked Responses Generated by Epidural and Transcutaneous Spinal Stimulation in Humans with Spinal Cord Injury |
title | Voluntary Modulation of Evoked Responses Generated by Epidural and Transcutaneous Spinal Stimulation in Humans with Spinal Cord Injury |
title_full | Voluntary Modulation of Evoked Responses Generated by Epidural and Transcutaneous Spinal Stimulation in Humans with Spinal Cord Injury |
title_fullStr | Voluntary Modulation of Evoked Responses Generated by Epidural and Transcutaneous Spinal Stimulation in Humans with Spinal Cord Injury |
title_full_unstemmed | Voluntary Modulation of Evoked Responses Generated by Epidural and Transcutaneous Spinal Stimulation in Humans with Spinal Cord Injury |
title_short | Voluntary Modulation of Evoked Responses Generated by Epidural and Transcutaneous Spinal Stimulation in Humans with Spinal Cord Injury |
title_sort | voluntary modulation of evoked responses generated by epidural and transcutaneous spinal stimulation in humans with spinal cord injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584516/ https://www.ncbi.nlm.nih.gov/pubmed/34768418 http://dx.doi.org/10.3390/jcm10214898 |
work_keys_str_mv | AT calvertjonathans voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT gillmeganl voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT lindemargauxb voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT veithdanield voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT thoresonandrewr voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT lopezcesar voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT leekendallh voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT gerasimenkoyuryp voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT edgertonvictorr voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT lavrovigora voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT zhaokristind voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT grahnpeterj voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury AT sayenkodimitryg voluntarymodulationofevokedresponsesgeneratedbyepiduralandtranscutaneousspinalstimulationinhumanswithspinalcordinjury |