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....

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Main Authors: Tsuyoshi Nakajima, Kiyotaka Kamibayashi, Taku Kitamura, Tomoyoshi Komiyama, E Paul Zehr, Kimitaka Nakazawa
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-07-01
Series:Frontiers in Human Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnhum.2016.00368/full
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author Tsuyoshi Nakajima
Kiyotaka Kamibayashi
Taku Kitamura
Tomoyoshi Komiyama
E Paul Zehr
Kimitaka Nakazawa
author_facet Tsuyoshi Nakajima
Kiyotaka Kamibayashi
Taku Kitamura
Tomoyoshi Komiyama
E Paul Zehr
Kimitaka Nakazawa
author_sort Tsuyoshi Nakajima
collection DOAJ
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 minutes of passive stepping was sufficient to elicit a persistent H-reflex suppression that lasted up to 15 minutes, 5 minutes 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.
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spelling doaj.art-9d778e12b560466893d94ddae2d7d9462022-12-21T18:29:53ZengFrontiers Media S.A.Frontiers in Human Neuroscience1662-51612016-07-011010.3389/fnhum.2016.00368197159Short-term plasticity in a monosynaptic reflex pathway to forearm muscles after continuous robot-assisted passive steppingTsuyoshi Nakajima0Kiyotaka Kamibayashi1Taku Kitamura2Tomoyoshi Komiyama3E Paul Zehr4Kimitaka Nakazawa5Kyorin unversity School of MedicineDoshisha UniversityResearch Institute, National Rehabilitation Center for Persons with DisabilitiesChiba UniversityUniversity of VictoriaUniversity of TokyoBoth 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 minutes of passive stepping was sufficient to elicit a persistent H-reflex suppression that lasted up to 15 minutes, 5 minutes 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.http://journal.frontiersin.org/Journal/10.3389/fnhum.2016.00368/fullHumansshort-term plasticityspinal reflexafferent feedbackPassive stepping
spellingShingle Tsuyoshi Nakajima
Kiyotaka Kamibayashi
Taku Kitamura
Tomoyoshi Komiyama
E Paul Zehr
Kimitaka Nakazawa
Short-term plasticity in a monosynaptic reflex pathway to forearm muscles after continuous robot-assisted passive stepping
Frontiers in Human Neuroscience
Humans
short-term plasticity
spinal reflex
afferent feedback
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 Humans
short-term plasticity
spinal reflex
afferent feedback
Passive stepping
url http://journal.frontiersin.org/Journal/10.3389/fnhum.2016.00368/full
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