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Neural Adaptations Associated with Interlimb Transfer in a Ballistic Wrist Flexion Task
Cross education is the process whereby training of one limb gives rise to increases in the subsequent performance of its opposite counterpart. The execution of many unilateral tasks is associated with increased excitability of corticospinal projections from primary motor cortex (M1) to the opposite...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853797/ https://www.ncbi.nlm.nih.gov/pubmed/27199722 http://dx.doi.org/10.3389/fnhum.2016.00204 |
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author | Ruddy, Kathy L. Rudolf, Anne K. Kalkman, Barbara King, Maedbh Daffertshofer, Andreas Carroll, Timothy J. Carson, Richard G. |
author_facet | Ruddy, Kathy L. Rudolf, Anne K. Kalkman, Barbara King, Maedbh Daffertshofer, Andreas Carroll, Timothy J. Carson, Richard G. |
author_sort | Ruddy, Kathy L. |
collection | PubMed |
description | Cross education is the process whereby training of one limb gives rise to increases in the subsequent performance of its opposite counterpart. The execution of many unilateral tasks is associated with increased excitability of corticospinal projections from primary motor cortex (M1) to the opposite limb. It has been proposed that these effects are causally related. Our aim was to establish whether changes in corticospinal excitability (CSE) arising from prior training of the opposite limb determine levels of interlimb transfer. We used three vision conditions shown previously to modulate the excitability of corticospinal projections to the inactive (right) limb during wrist flexion movements performed by the training (left) limb. These were: (1) mirrored visual feedback of the training limb; (2) no visual feedback of either limb; and (3) visual feedback of the inactive limb. Training comprised 300 discrete, ballistic wrist flexion movements executed as rapidly as possible. Performance of the right limb on the same task was assessed prior to, at the mid point of, and following left limb training. There was no evidence that variations in the excitability of corticospinal projections (assessed by transcranial magnetic stimulation (TMS)) to the inactive limb were associated with, or predictive of, the extent of interlimb transfer that was expressed. There were however associations between alterations in muscle activation dynamics observed for the untrained limb, and the degree of positive transfer that arose from training of the opposite limb. The results suggest that the acute adaptations that mediate the bilateral performance gains realized through unilateral practice of this ballistic wrist flexion task are mediated by neural elements other than those within M1 that are recruited at rest by single-pulse TMS. |
format | Online Article Text |
id | pubmed-4853797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48537972016-05-19 Neural Adaptations Associated with Interlimb Transfer in a Ballistic Wrist Flexion Task Ruddy, Kathy L. Rudolf, Anne K. Kalkman, Barbara King, Maedbh Daffertshofer, Andreas Carroll, Timothy J. Carson, Richard G. Front Hum Neurosci Neuroscience Cross education is the process whereby training of one limb gives rise to increases in the subsequent performance of its opposite counterpart. The execution of many unilateral tasks is associated with increased excitability of corticospinal projections from primary motor cortex (M1) to the opposite limb. It has been proposed that these effects are causally related. Our aim was to establish whether changes in corticospinal excitability (CSE) arising from prior training of the opposite limb determine levels of interlimb transfer. We used three vision conditions shown previously to modulate the excitability of corticospinal projections to the inactive (right) limb during wrist flexion movements performed by the training (left) limb. These were: (1) mirrored visual feedback of the training limb; (2) no visual feedback of either limb; and (3) visual feedback of the inactive limb. Training comprised 300 discrete, ballistic wrist flexion movements executed as rapidly as possible. Performance of the right limb on the same task was assessed prior to, at the mid point of, and following left limb training. There was no evidence that variations in the excitability of corticospinal projections (assessed by transcranial magnetic stimulation (TMS)) to the inactive limb were associated with, or predictive of, the extent of interlimb transfer that was expressed. There were however associations between alterations in muscle activation dynamics observed for the untrained limb, and the degree of positive transfer that arose from training of the opposite limb. The results suggest that the acute adaptations that mediate the bilateral performance gains realized through unilateral practice of this ballistic wrist flexion task are mediated by neural elements other than those within M1 that are recruited at rest by single-pulse TMS. Frontiers Media S.A. 2016-05-03 /pmc/articles/PMC4853797/ /pubmed/27199722 http://dx.doi.org/10.3389/fnhum.2016.00204 Text en Copyright © 2016 Ruddy, Rudolf, Kalkman, King, Daffertshofer, Carroll and Carson. 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 Ruddy, Kathy L. Rudolf, Anne K. Kalkman, Barbara King, Maedbh Daffertshofer, Andreas Carroll, Timothy J. Carson, Richard G. Neural Adaptations Associated with Interlimb Transfer in a Ballistic Wrist Flexion Task |
title | Neural Adaptations Associated with Interlimb Transfer in a Ballistic Wrist Flexion Task |
title_full | Neural Adaptations Associated with Interlimb Transfer in a Ballistic Wrist Flexion Task |
title_fullStr | Neural Adaptations Associated with Interlimb Transfer in a Ballistic Wrist Flexion Task |
title_full_unstemmed | Neural Adaptations Associated with Interlimb Transfer in a Ballistic Wrist Flexion Task |
title_short | Neural Adaptations Associated with Interlimb Transfer in a Ballistic Wrist Flexion Task |
title_sort | neural adaptations associated with interlimb transfer in a ballistic wrist flexion task |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853797/ https://www.ncbi.nlm.nih.gov/pubmed/27199722 http://dx.doi.org/10.3389/fnhum.2016.00204 |
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