Cargando…

Neural Substrates of Cognitive Motor Interference During Walking; Peripheral and Central Mechanisms

Current gait control models suggest that independent locomotion depends on central and peripheral mechanisms. However, less information is available on the integration of these mechanisms for adaptive walking. In this cross-sectional study, we investigated gait control mechanisms in people with Park...

Descripción completa

Detalles Bibliográficos
Autores principales: Al-Yahya, Emad, Mahmoud, Wala’, Meester, Daan, Esser, Patrick, Dawes, Helen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333849/
https://www.ncbi.nlm.nih.gov/pubmed/30687049
http://dx.doi.org/10.3389/fnhum.2018.00536
_version_ 1783387632125870080
author Al-Yahya, Emad
Mahmoud, Wala’
Meester, Daan
Esser, Patrick
Dawes, Helen
author_facet Al-Yahya, Emad
Mahmoud, Wala’
Meester, Daan
Esser, Patrick
Dawes, Helen
author_sort Al-Yahya, Emad
collection PubMed
description Current gait control models suggest that independent locomotion depends on central and peripheral mechanisms. However, less information is available on the integration of these mechanisms for adaptive walking. In this cross-sectional study, we investigated gait control mechanisms in people with Parkinson’s disease (PD) and healthy older (HO) adults: at self-selected walking speed (SSWS) and at fast walking speed (FWS). We measured effect of additional cognitive task (DT) and increased speed on prefrontal (PFC) and motor cortex (M1) activation, and Soleus H-reflex gain. Under DT-conditions we observed increased activation in PFC and M1. Whilst H-reflex gain decreased with additional cognitive load for both groups and speeds, H-reflex gain was lower in PD compared to HO while walking under ST condition at SSWS. Attentional load in PFC excites M1, which in turn increases inhibition on H-reflex activity during walking and reduces activity and sensitivity of peripheral reflex during the stance phase of gait. Importantly this effect on sensitivity was greater in HO. We have previously observed that the PFC copes with increased attentional load in young adults with no impact on peripheral reflexes and we suggest that gait instability in PD may in part be due to altered sensorimotor functioning reducing the sensitivity of peripheral reflexes.
format Online
Article
Text
id pubmed-6333849
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-63338492019-01-25 Neural Substrates of Cognitive Motor Interference During Walking; Peripheral and Central Mechanisms Al-Yahya, Emad Mahmoud, Wala’ Meester, Daan Esser, Patrick Dawes, Helen Front Hum Neurosci Neuroscience Current gait control models suggest that independent locomotion depends on central and peripheral mechanisms. However, less information is available on the integration of these mechanisms for adaptive walking. In this cross-sectional study, we investigated gait control mechanisms in people with Parkinson’s disease (PD) and healthy older (HO) adults: at self-selected walking speed (SSWS) and at fast walking speed (FWS). We measured effect of additional cognitive task (DT) and increased speed on prefrontal (PFC) and motor cortex (M1) activation, and Soleus H-reflex gain. Under DT-conditions we observed increased activation in PFC and M1. Whilst H-reflex gain decreased with additional cognitive load for both groups and speeds, H-reflex gain was lower in PD compared to HO while walking under ST condition at SSWS. Attentional load in PFC excites M1, which in turn increases inhibition on H-reflex activity during walking and reduces activity and sensitivity of peripheral reflex during the stance phase of gait. Importantly this effect on sensitivity was greater in HO. We have previously observed that the PFC copes with increased attentional load in young adults with no impact on peripheral reflexes and we suggest that gait instability in PD may in part be due to altered sensorimotor functioning reducing the sensitivity of peripheral reflexes. Frontiers Media S.A. 2019-01-09 /pmc/articles/PMC6333849/ /pubmed/30687049 http://dx.doi.org/10.3389/fnhum.2018.00536 Text en Copyright © 2019 Al-Yahya, Mahmoud, Meester, Esser and Dawes. 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 Neuroscience
Al-Yahya, Emad
Mahmoud, Wala’
Meester, Daan
Esser, Patrick
Dawes, Helen
Neural Substrates of Cognitive Motor Interference During Walking; Peripheral and Central Mechanisms
title Neural Substrates of Cognitive Motor Interference During Walking; Peripheral and Central Mechanisms
title_full Neural Substrates of Cognitive Motor Interference During Walking; Peripheral and Central Mechanisms
title_fullStr Neural Substrates of Cognitive Motor Interference During Walking; Peripheral and Central Mechanisms
title_full_unstemmed Neural Substrates of Cognitive Motor Interference During Walking; Peripheral and Central Mechanisms
title_short Neural Substrates of Cognitive Motor Interference During Walking; Peripheral and Central Mechanisms
title_sort neural substrates of cognitive motor interference during walking; peripheral and central mechanisms
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333849/
https://www.ncbi.nlm.nih.gov/pubmed/30687049
http://dx.doi.org/10.3389/fnhum.2018.00536
work_keys_str_mv AT alyahyaemad neuralsubstratesofcognitivemotorinterferenceduringwalkingperipheralandcentralmechanisms
AT mahmoudwala neuralsubstratesofcognitivemotorinterferenceduringwalkingperipheralandcentralmechanisms
AT meesterdaan neuralsubstratesofcognitivemotorinterferenceduringwalkingperipheralandcentralmechanisms
AT esserpatrick neuralsubstratesofcognitivemotorinterferenceduringwalkingperipheralandcentralmechanisms
AT daweshelen neuralsubstratesofcognitivemotorinterferenceduringwalkingperipheralandcentralmechanisms