Cargando…

Short-Term Plasticity in a Monosynaptic Reflex Pathway to Forearm Muscles after Continuous Robot-Assisted Passive Stepping

Both active and passive rhythmic limb movements reduce the amplitude of spinal cord Hoffmann (H-) reflexes in muscles of moving and distant limbs. This could have clinical utility in remote modulation of the pathologically hyperactive reflexes found in spasticity after stroke or spinal cord injury....

Descripción completa

Detalles Bibliográficos
Autores principales: Nakajima, Tsuyoshi, Kamibayashi, Kiyotaka, Kitamura, Taku, Komiyama, Tomoyoshi, Zehr, E. Paul, Nakazawa, Kimitaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956673/
https://www.ncbi.nlm.nih.gov/pubmed/27499737
http://dx.doi.org/10.3389/fnhum.2016.00368
_version_ 1782444052017315840
author Nakajima, Tsuyoshi
Kamibayashi, Kiyotaka
Kitamura, Taku
Komiyama, Tomoyoshi
Zehr, E. Paul
Nakazawa, Kimitaka
author_facet Nakajima, Tsuyoshi
Kamibayashi, Kiyotaka
Kitamura, Taku
Komiyama, Tomoyoshi
Zehr, E. Paul
Nakazawa, Kimitaka
author_sort Nakajima, Tsuyoshi
collection PubMed
description Both active and passive rhythmic limb movements reduce the amplitude of spinal cord Hoffmann (H-) reflexes in muscles of moving and distant limbs. This could have clinical utility in remote modulation of the pathologically hyperactive reflexes found in spasticity after stroke or spinal cord injury. However, such clinical translation is currently hampered by a lack of critical information regarding the minimum or effective duration of passive movement needed for modulating spinal cord excitability. We therefore investigated the H-reflex modulation in the flexor carpi radialis (FCR) muscle during and after various durations (5, 10, 15, and 30 min) of passive stepping in 11 neurologically normal subjects. Passive stepping was performed by a robotic gait trainer system (Lokomat(®)) while a single pulse of electrical stimulation to the median nerve elicited H-reflexes in the FCR. The amplitude of the FCR H-reflex was significantly suppressed during passive stepping. Although 30 min of passive stepping was sufficient to elicit a persistent H-reflex suppression that lasted up to 15 min, 5 min of passive stepping was not. The duration of H-reflex suppression correlated with that of the stepping. These findings suggest that the accumulation of stepping-related afferent feedback from the leg plays a role in generating short-term interlimb plasticity in the circuitry of the FCR H-reflex.
format Online
Article
Text
id pubmed-4956673
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-49566732016-08-05 Short-Term Plasticity in a Monosynaptic Reflex Pathway to Forearm Muscles after Continuous Robot-Assisted Passive Stepping Nakajima, Tsuyoshi Kamibayashi, Kiyotaka Kitamura, Taku Komiyama, Tomoyoshi Zehr, E. Paul Nakazawa, Kimitaka Front Hum Neurosci Neuroscience Both active and passive rhythmic limb movements reduce the amplitude of spinal cord Hoffmann (H-) reflexes in muscles of moving and distant limbs. This could have clinical utility in remote modulation of the pathologically hyperactive reflexes found in spasticity after stroke or spinal cord injury. However, such clinical translation is currently hampered by a lack of critical information regarding the minimum or effective duration of passive movement needed for modulating spinal cord excitability. We therefore investigated the H-reflex modulation in the flexor carpi radialis (FCR) muscle during and after various durations (5, 10, 15, and 30 min) of passive stepping in 11 neurologically normal subjects. Passive stepping was performed by a robotic gait trainer system (Lokomat(®)) while a single pulse of electrical stimulation to the median nerve elicited H-reflexes in the FCR. The amplitude of the FCR H-reflex was significantly suppressed during passive stepping. Although 30 min of passive stepping was sufficient to elicit a persistent H-reflex suppression that lasted up to 15 min, 5 min of passive stepping was not. The duration of H-reflex suppression correlated with that of the stepping. These findings suggest that the accumulation of stepping-related afferent feedback from the leg plays a role in generating short-term interlimb plasticity in the circuitry of the FCR H-reflex. Frontiers Media S.A. 2016-07-22 /pmc/articles/PMC4956673/ /pubmed/27499737 http://dx.doi.org/10.3389/fnhum.2016.00368 Text en Copyright © 2016 Nakajima, Kamibayashi, Kitamura, Komiyama, Zehr and Nakazawa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Nakajima, Tsuyoshi
Kamibayashi, Kiyotaka
Kitamura, Taku
Komiyama, Tomoyoshi
Zehr, E. Paul
Nakazawa, Kimitaka
Short-Term Plasticity in a Monosynaptic Reflex Pathway to Forearm Muscles after Continuous Robot-Assisted Passive Stepping
title Short-Term Plasticity in a Monosynaptic Reflex Pathway to Forearm Muscles after Continuous Robot-Assisted Passive Stepping
title_full Short-Term Plasticity in a Monosynaptic Reflex Pathway to Forearm Muscles after Continuous Robot-Assisted Passive Stepping
title_fullStr Short-Term Plasticity in a Monosynaptic Reflex Pathway to Forearm Muscles after Continuous Robot-Assisted Passive Stepping
title_full_unstemmed Short-Term Plasticity in a Monosynaptic Reflex Pathway to Forearm Muscles after Continuous Robot-Assisted Passive Stepping
title_short Short-Term Plasticity in a Monosynaptic Reflex Pathway to Forearm Muscles after Continuous Robot-Assisted Passive Stepping
title_sort short-term plasticity in a monosynaptic reflex pathway to forearm muscles after continuous robot-assisted passive stepping
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956673/
https://www.ncbi.nlm.nih.gov/pubmed/27499737
http://dx.doi.org/10.3389/fnhum.2016.00368
work_keys_str_mv AT nakajimatsuyoshi shorttermplasticityinamonosynapticreflexpathwaytoforearmmusclesaftercontinuousrobotassistedpassivestepping
AT kamibayashikiyotaka shorttermplasticityinamonosynapticreflexpathwaytoforearmmusclesaftercontinuousrobotassistedpassivestepping
AT kitamurataku shorttermplasticityinamonosynapticreflexpathwaytoforearmmusclesaftercontinuousrobotassistedpassivestepping
AT komiyamatomoyoshi shorttermplasticityinamonosynapticreflexpathwaytoforearmmusclesaftercontinuousrobotassistedpassivestepping
AT zehrepaul shorttermplasticityinamonosynapticreflexpathwaytoforearmmusclesaftercontinuousrobotassistedpassivestepping
AT nakazawakimitaka shorttermplasticityinamonosynapticreflexpathwaytoforearmmusclesaftercontinuousrobotassistedpassivestepping