Cargando…

Short Intracortical Inhibition During Voluntary Movement Reveals Persistent Impairment Post-stroke

Objective: Short intracortical inhibition (SICI) is a GABA(A)-mediated phenomenon, argued to mediate selective muscle activation during coordinated motor activity. Markedly reduced SICI has been observed in the acute period following stroke and, based on findings in animal models, it has been posite...

Descripción completa

Detalles Bibliográficos
Autores principales: Ding, Qian, Triggs, William J., Kamath, Sahana M., Patten, Carolynn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328452/
https://www.ncbi.nlm.nih.gov/pubmed/30662425
http://dx.doi.org/10.3389/fneur.2018.01105
_version_ 1783386643094306816
author Ding, Qian
Triggs, William J.
Kamath, Sahana M.
Patten, Carolynn
author_facet Ding, Qian
Triggs, William J.
Kamath, Sahana M.
Patten, Carolynn
author_sort Ding, Qian
collection PubMed
description Objective: Short intracortical inhibition (SICI) is a GABA(A)-mediated phenomenon, argued to mediate selective muscle activation during coordinated motor activity. Markedly reduced SICI has been observed in the acute period following stroke and, based on findings in animal models, it has been posited this disinhibitory phenomenon may facilitate neural plasticity and contribute to early motor recovery. However, it remains unresolved whether SICI normalizes over time, as part of the natural course of stroke recovery. Whether intracortical inhibition contributes to motor recovery in chronic stroke also remains unclear. Notably, SICI is typically measured at rest, which may not fully reveal its role in motor control. Here we investigated SICI at rest and during voluntary motor activity to determine: (1) whether GABA(A)-mediated inhibition recovers, and (2) how GABA(A)-mediated inhibition is related to motor function, in the chronic phase post-stroke. Methods: We studied 16 chronic stroke survivors (age: 64.6 ± 9.3 years; chronicity: 74.3 ± 52.9 months) and 12 age-matched healthy controls. We used paired-pulse transcranial magnetic stimulation (TMS) to induce SICI during three conditions: rest, submaximal grip, and performance of box-and-blocks. Upper-extremity Fugl-Meyer Assessment and Box-and-Blocks tests were used to evaluate motor impairment in stroke survivors and manual dexterity in all participants, respectively. Results: At rest, SICI revealed no differences between ipsilesional and contralesional hemispheres of either cortical or subcortical stroke survivors, or healthy controls (P's > 0.05). During box-and-blocks, however, ipsilesional hemisphere SICI was significantly reduced (P = 0.025), especially following cortical stroke (P < 0.001). SICI in the ipsilesional hemisphere during box-and-blocks task was significantly related to paretic hand dexterity (r = 0.56, P = 0.039) and motor impairment (r = 0.56, P = 0.037). Conclusions: SICI during motor activity, but not rest, reveals persistent impairment in chronic stroke survivors indicating that inhibitory brain circuits responsible for motor coordination do not fully normalize as part of the natural history of stroke recovery. Observation that reduced SICI (i.e., disinhibition) is associated with greater motor impairment and worse dexterity in chronic hemiparetic individuals suggests the response considered to promote neuroplasticity and recovery in the acute phase could be maladaptive in the chronic phase post-stroke.
format Online
Article
Text
id pubmed-6328452
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-63284522019-01-18 Short Intracortical Inhibition During Voluntary Movement Reveals Persistent Impairment Post-stroke Ding, Qian Triggs, William J. Kamath, Sahana M. Patten, Carolynn Front Neurol Neurology Objective: Short intracortical inhibition (SICI) is a GABA(A)-mediated phenomenon, argued to mediate selective muscle activation during coordinated motor activity. Markedly reduced SICI has been observed in the acute period following stroke and, based on findings in animal models, it has been posited this disinhibitory phenomenon may facilitate neural plasticity and contribute to early motor recovery. However, it remains unresolved whether SICI normalizes over time, as part of the natural course of stroke recovery. Whether intracortical inhibition contributes to motor recovery in chronic stroke also remains unclear. Notably, SICI is typically measured at rest, which may not fully reveal its role in motor control. Here we investigated SICI at rest and during voluntary motor activity to determine: (1) whether GABA(A)-mediated inhibition recovers, and (2) how GABA(A)-mediated inhibition is related to motor function, in the chronic phase post-stroke. Methods: We studied 16 chronic stroke survivors (age: 64.6 ± 9.3 years; chronicity: 74.3 ± 52.9 months) and 12 age-matched healthy controls. We used paired-pulse transcranial magnetic stimulation (TMS) to induce SICI during three conditions: rest, submaximal grip, and performance of box-and-blocks. Upper-extremity Fugl-Meyer Assessment and Box-and-Blocks tests were used to evaluate motor impairment in stroke survivors and manual dexterity in all participants, respectively. Results: At rest, SICI revealed no differences between ipsilesional and contralesional hemispheres of either cortical or subcortical stroke survivors, or healthy controls (P's > 0.05). During box-and-blocks, however, ipsilesional hemisphere SICI was significantly reduced (P = 0.025), especially following cortical stroke (P < 0.001). SICI in the ipsilesional hemisphere during box-and-blocks task was significantly related to paretic hand dexterity (r = 0.56, P = 0.039) and motor impairment (r = 0.56, P = 0.037). Conclusions: SICI during motor activity, but not rest, reveals persistent impairment in chronic stroke survivors indicating that inhibitory brain circuits responsible for motor coordination do not fully normalize as part of the natural history of stroke recovery. Observation that reduced SICI (i.e., disinhibition) is associated with greater motor impairment and worse dexterity in chronic hemiparetic individuals suggests the response considered to promote neuroplasticity and recovery in the acute phase could be maladaptive in the chronic phase post-stroke. Frontiers Media S.A. 2019-01-04 /pmc/articles/PMC6328452/ /pubmed/30662425 http://dx.doi.org/10.3389/fneur.2018.01105 Text en Copyright © 2019 Ding, Triggs, Kamath and Patten. 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 or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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 Neurology
Ding, Qian
Triggs, William J.
Kamath, Sahana M.
Patten, Carolynn
Short Intracortical Inhibition During Voluntary Movement Reveals Persistent Impairment Post-stroke
title Short Intracortical Inhibition During Voluntary Movement Reveals Persistent Impairment Post-stroke
title_full Short Intracortical Inhibition During Voluntary Movement Reveals Persistent Impairment Post-stroke
title_fullStr Short Intracortical Inhibition During Voluntary Movement Reveals Persistent Impairment Post-stroke
title_full_unstemmed Short Intracortical Inhibition During Voluntary Movement Reveals Persistent Impairment Post-stroke
title_short Short Intracortical Inhibition During Voluntary Movement Reveals Persistent Impairment Post-stroke
title_sort short intracortical inhibition during voluntary movement reveals persistent impairment post-stroke
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328452/
https://www.ncbi.nlm.nih.gov/pubmed/30662425
http://dx.doi.org/10.3389/fneur.2018.01105
work_keys_str_mv AT dingqian shortintracorticalinhibitionduringvoluntarymovementrevealspersistentimpairmentpoststroke
AT triggswilliamj shortintracorticalinhibitionduringvoluntarymovementrevealspersistentimpairmentpoststroke
AT kamathsahanam shortintracorticalinhibitionduringvoluntarymovementrevealspersistentimpairmentpoststroke
AT pattencarolynn shortintracorticalinhibitionduringvoluntarymovementrevealspersistentimpairmentpoststroke