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Integrating Brain and Biomechanical Models—A New Paradigm for Understanding Neuro-muscular Control

To date, realistic models of how the central nervous system governs behavior have been restricted in scope to the brain, brainstem or spinal column, as if these existed as disembodied organs. Further, the model is often exercised in relation to an in vivo physiological experiment with input comprisi...

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Autores principales: James, Sebastian S., Papapavlou, Chris, Blenkinsop, Alexander, Cope, Alexander J., Anderson, Sean R., Moustakas, Konstantinos, Gurney, Kevin N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808253/
https://www.ncbi.nlm.nih.gov/pubmed/29467606
http://dx.doi.org/10.3389/fnins.2018.00039
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author James, Sebastian S.
Papapavlou, Chris
Blenkinsop, Alexander
Cope, Alexander J.
Anderson, Sean R.
Moustakas, Konstantinos
Gurney, Kevin N.
author_facet James, Sebastian S.
Papapavlou, Chris
Blenkinsop, Alexander
Cope, Alexander J.
Anderson, Sean R.
Moustakas, Konstantinos
Gurney, Kevin N.
author_sort James, Sebastian S.
collection PubMed
description To date, realistic models of how the central nervous system governs behavior have been restricted in scope to the brain, brainstem or spinal column, as if these existed as disembodied organs. Further, the model is often exercised in relation to an in vivo physiological experiment with input comprising an impulse, a periodic signal or constant activation, and output as a pattern of neural activity in one or more neural populations. Any link to behavior is inferred only indirectly via these activity patterns. We argue that to discover the principles of operation of neural systems, it is necessary to express their behavior in terms of physical movements of a realistic motor system, and to supply inputs that mimic sensory experience. To do this with confidence, we must connect our brain models to neuro-muscular models and provide relevant visual and proprioceptive feedback signals, thereby closing the loop of the simulation. This paper describes an effort to develop just such an integrated brain and biomechanical system using a number of pre-existing models. It describes a model of the saccadic oculomotor system incorporating a neuromuscular model of the eye and its six extraocular muscles. The position of the eye determines how illumination of a retinotopic input population projects information about the location of a saccade target into the system. A pre-existing saccadic burst generator model was incorporated into the system, which generated motoneuron activity patterns suitable for driving the biomechanical eye. The model was demonstrated to make accurate saccades to a target luminance under a set of environmental constraints. Challenges encountered in the development of this model showed the importance of this integrated modeling approach. Thus, we exposed shortcomings in individual model components which were only apparent when these were supplied with the more plausible inputs available in a closed loop design. Consequently we were able to suggest missing functionality which the system would require to reproduce more realistic behavior. The construction of such closed-loop animal models constitutes a new paradigm of computational neurobehavior and promises a more thoroughgoing approach to our understanding of the brain's function as a controller for movement and behavior.
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spelling pubmed-58082532018-02-21 Integrating Brain and Biomechanical Models—A New Paradigm for Understanding Neuro-muscular Control James, Sebastian S. Papapavlou, Chris Blenkinsop, Alexander Cope, Alexander J. Anderson, Sean R. Moustakas, Konstantinos Gurney, Kevin N. Front Neurosci Neuroscience To date, realistic models of how the central nervous system governs behavior have been restricted in scope to the brain, brainstem or spinal column, as if these existed as disembodied organs. Further, the model is often exercised in relation to an in vivo physiological experiment with input comprising an impulse, a periodic signal or constant activation, and output as a pattern of neural activity in one or more neural populations. Any link to behavior is inferred only indirectly via these activity patterns. We argue that to discover the principles of operation of neural systems, it is necessary to express their behavior in terms of physical movements of a realistic motor system, and to supply inputs that mimic sensory experience. To do this with confidence, we must connect our brain models to neuro-muscular models and provide relevant visual and proprioceptive feedback signals, thereby closing the loop of the simulation. This paper describes an effort to develop just such an integrated brain and biomechanical system using a number of pre-existing models. It describes a model of the saccadic oculomotor system incorporating a neuromuscular model of the eye and its six extraocular muscles. The position of the eye determines how illumination of a retinotopic input population projects information about the location of a saccade target into the system. A pre-existing saccadic burst generator model was incorporated into the system, which generated motoneuron activity patterns suitable for driving the biomechanical eye. The model was demonstrated to make accurate saccades to a target luminance under a set of environmental constraints. Challenges encountered in the development of this model showed the importance of this integrated modeling approach. Thus, we exposed shortcomings in individual model components which were only apparent when these were supplied with the more plausible inputs available in a closed loop design. Consequently we were able to suggest missing functionality which the system would require to reproduce more realistic behavior. The construction of such closed-loop animal models constitutes a new paradigm of computational neurobehavior and promises a more thoroughgoing approach to our understanding of the brain's function as a controller for movement and behavior. Frontiers Media S.A. 2018-02-06 /pmc/articles/PMC5808253/ /pubmed/29467606 http://dx.doi.org/10.3389/fnins.2018.00039 Text en Copyright © 2018 James, Papapavlou, Blenkinsop, Cope, Anderson, Moustakas and Gurney. 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 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
James, Sebastian S.
Papapavlou, Chris
Blenkinsop, Alexander
Cope, Alexander J.
Anderson, Sean R.
Moustakas, Konstantinos
Gurney, Kevin N.
Integrating Brain and Biomechanical Models—A New Paradigm for Understanding Neuro-muscular Control
title Integrating Brain and Biomechanical Models—A New Paradigm for Understanding Neuro-muscular Control
title_full Integrating Brain and Biomechanical Models—A New Paradigm for Understanding Neuro-muscular Control
title_fullStr Integrating Brain and Biomechanical Models—A New Paradigm for Understanding Neuro-muscular Control
title_full_unstemmed Integrating Brain and Biomechanical Models—A New Paradigm for Understanding Neuro-muscular Control
title_short Integrating Brain and Biomechanical Models—A New Paradigm for Understanding Neuro-muscular Control
title_sort integrating brain and biomechanical models—a new paradigm for understanding neuro-muscular control
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808253/
https://www.ncbi.nlm.nih.gov/pubmed/29467606
http://dx.doi.org/10.3389/fnins.2018.00039
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