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A Pathological Condition Affects Motor Modules in a Bipedal Locomotion Model

Bipedal locomotion is a basic motor activity that requires simultaneous control of multiple muscles. Physiological experiments suggest that the nervous system controls bipedal locomotion efficiently by using motor modules of synergistic muscle activations. If these modules were merged, abnormal loco...

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Autores principales: Ichimura, Daisuke, Yamazaki, Tadashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763684/
https://www.ncbi.nlm.nih.gov/pubmed/31616276
http://dx.doi.org/10.3389/fnbot.2019.00079
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author Ichimura, Daisuke
Yamazaki, Tadashi
author_facet Ichimura, Daisuke
Yamazaki, Tadashi
author_sort Ichimura, Daisuke
collection PubMed
description Bipedal locomotion is a basic motor activity that requires simultaneous control of multiple muscles. Physiological experiments suggest that the nervous system controls bipedal locomotion efficiently by using motor modules of synergistic muscle activations. If these modules were merged, abnormal locomotion patterns would be realized as observed in patients with neural impairments such as chronic stroke. However, sub-acute patients have been reported not to show such merged motor modules. Therefore, in this study, we examined what conditions in the nervous system merges motor modules. we built a two-dimensional bipedal locomotion model that included a musculoskeletal model with 7 segments and 18 muscles, a neural system with a hierarchical central pattern generator (CPG), and various feedback inputs from reflex organs. The CPG generated synergistic muscle activations comprising 5 motor modules to produce locomotion phases. Our model succeeded to acquire stable locomotion by using the motor modules and reflexes. Next, we examined how a pathological condition altered motor modules. Specifically, we weakened neural inputs to muscles on one leg to simulate a stroke condition. Immediately after the simulated stroke, the model did not walk. Then, internal parameters were modified to recover stable locomotion. We refitted either (a) reflex parameters or (b) CPG parameters to compensate the locomotion by adapting (a) reflexes or (b) the controller. Stable locomotion was recovered in both conditions. However the motor modules were merged only in (b). These results suggest that light or sub-acute stroke patients, who can compensate stable locomotion by just adapting reflexes, would not show merge of motor modules, whereas severe or chronic patients, who needed to adapt the controller for compensation, would show the merge, as consistent with experimental findings.
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spelling pubmed-67636842019-10-15 A Pathological Condition Affects Motor Modules in a Bipedal Locomotion Model Ichimura, Daisuke Yamazaki, Tadashi Front Neurorobot Neuroscience Bipedal locomotion is a basic motor activity that requires simultaneous control of multiple muscles. Physiological experiments suggest that the nervous system controls bipedal locomotion efficiently by using motor modules of synergistic muscle activations. If these modules were merged, abnormal locomotion patterns would be realized as observed in patients with neural impairments such as chronic stroke. However, sub-acute patients have been reported not to show such merged motor modules. Therefore, in this study, we examined what conditions in the nervous system merges motor modules. we built a two-dimensional bipedal locomotion model that included a musculoskeletal model with 7 segments and 18 muscles, a neural system with a hierarchical central pattern generator (CPG), and various feedback inputs from reflex organs. The CPG generated synergistic muscle activations comprising 5 motor modules to produce locomotion phases. Our model succeeded to acquire stable locomotion by using the motor modules and reflexes. Next, we examined how a pathological condition altered motor modules. Specifically, we weakened neural inputs to muscles on one leg to simulate a stroke condition. Immediately after the simulated stroke, the model did not walk. Then, internal parameters were modified to recover stable locomotion. We refitted either (a) reflex parameters or (b) CPG parameters to compensate the locomotion by adapting (a) reflexes or (b) the controller. Stable locomotion was recovered in both conditions. However the motor modules were merged only in (b). These results suggest that light or sub-acute stroke patients, who can compensate stable locomotion by just adapting reflexes, would not show merge of motor modules, whereas severe or chronic patients, who needed to adapt the controller for compensation, would show the merge, as consistent with experimental findings. Frontiers Media S.A. 2019-09-20 /pmc/articles/PMC6763684/ /pubmed/31616276 http://dx.doi.org/10.3389/fnbot.2019.00079 Text en Copyright © 2019 Ichimura and Yamazaki. 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
Ichimura, Daisuke
Yamazaki, Tadashi
A Pathological Condition Affects Motor Modules in a Bipedal Locomotion Model
title A Pathological Condition Affects Motor Modules in a Bipedal Locomotion Model
title_full A Pathological Condition Affects Motor Modules in a Bipedal Locomotion Model
title_fullStr A Pathological Condition Affects Motor Modules in a Bipedal Locomotion Model
title_full_unstemmed A Pathological Condition Affects Motor Modules in a Bipedal Locomotion Model
title_short A Pathological Condition Affects Motor Modules in a Bipedal Locomotion Model
title_sort pathological condition affects motor modules in a bipedal locomotion model
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763684/
https://www.ncbi.nlm.nih.gov/pubmed/31616276
http://dx.doi.org/10.3389/fnbot.2019.00079
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