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Evolutionary autonomous agents and the nature of apraxia

BACKGROUND: Evolutionary autonomous agents are robots or robot simulations whose controller is a dynamical neural network and whose evolution occurs autonomously under the guidance of a fitness function without the detailed or explicit direction of an external programmer. They are embodied agents wi...

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Autores principales: Borrett, Donald S, Jin, Frank, Kwan, Hon C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC544844/
https://www.ncbi.nlm.nih.gov/pubmed/15631635
http://dx.doi.org/10.1186/1475-925X-4-1
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author Borrett, Donald S
Jin, Frank
Kwan, Hon C
author_facet Borrett, Donald S
Jin, Frank
Kwan, Hon C
author_sort Borrett, Donald S
collection PubMed
description BACKGROUND: Evolutionary autonomous agents are robots or robot simulations whose controller is a dynamical neural network and whose evolution occurs autonomously under the guidance of a fitness function without the detailed or explicit direction of an external programmer. They are embodied agents with a simple neural network controller and as such they provide the optimal forum by which sensorimotor interactions in a specified environment can be studied without the computational assumptions inherent in standard neuroscience. METHODS: Evolutionary autonomous agents were evolved that were able to perform identical movements under two different contexts, one which represented an automatic movement and one which had a symbolic context. In an attempt to model the automatic-voluntary dissociation frequently seen in ideomotor apraxia, lesions were introduced into the neural network controllers resulting in a behavioral dissociation with loss of the ability to perform the movement which had a symbolic context and preservation of the simpler, automatic movement. RESULTS: Analysis of the changes in the hierarchical organization of the networks in the apractic EAAs demonstrated consistent changes in the network dynamics across all agents with loss of longer duration time scales in the network dynamics. CONCLUSION: The concepts of determinate motor programs and perceptual representations that are implicit in the present day understanding of ideomotor apraxia are assumptions inherent in the computational understanding of brain function. The strength of the present study using EAAs to model one aspect of ideomotor apraxia is the absence of these assumptions and a grounding of all sensorimotor interactions in an embodied, autonomous agent. The consistency of the hierarchical changes in the network dynamics across all apractic agents demonstrates that this technique is tenable and will be a valuable adjunct to a computational formalism in the understanding of the physical basis of neurological disorders.
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spelling pubmed-5448442005-01-21 Evolutionary autonomous agents and the nature of apraxia Borrett, Donald S Jin, Frank Kwan, Hon C Biomed Eng Online Research BACKGROUND: Evolutionary autonomous agents are robots or robot simulations whose controller is a dynamical neural network and whose evolution occurs autonomously under the guidance of a fitness function without the detailed or explicit direction of an external programmer. They are embodied agents with a simple neural network controller and as such they provide the optimal forum by which sensorimotor interactions in a specified environment can be studied without the computational assumptions inherent in standard neuroscience. METHODS: Evolutionary autonomous agents were evolved that were able to perform identical movements under two different contexts, one which represented an automatic movement and one which had a symbolic context. In an attempt to model the automatic-voluntary dissociation frequently seen in ideomotor apraxia, lesions were introduced into the neural network controllers resulting in a behavioral dissociation with loss of the ability to perform the movement which had a symbolic context and preservation of the simpler, automatic movement. RESULTS: Analysis of the changes in the hierarchical organization of the networks in the apractic EAAs demonstrated consistent changes in the network dynamics across all agents with loss of longer duration time scales in the network dynamics. CONCLUSION: The concepts of determinate motor programs and perceptual representations that are implicit in the present day understanding of ideomotor apraxia are assumptions inherent in the computational understanding of brain function. The strength of the present study using EAAs to model one aspect of ideomotor apraxia is the absence of these assumptions and a grounding of all sensorimotor interactions in an embodied, autonomous agent. The consistency of the hierarchical changes in the network dynamics across all apractic agents demonstrates that this technique is tenable and will be a valuable adjunct to a computational formalism in the understanding of the physical basis of neurological disorders. BioMed Central 2005-01-04 /pmc/articles/PMC544844/ /pubmed/15631635 http://dx.doi.org/10.1186/1475-925X-4-1 Text en Copyright © 2005 Borrett et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Borrett, Donald S
Jin, Frank
Kwan, Hon C
Evolutionary autonomous agents and the nature of apraxia
title Evolutionary autonomous agents and the nature of apraxia
title_full Evolutionary autonomous agents and the nature of apraxia
title_fullStr Evolutionary autonomous agents and the nature of apraxia
title_full_unstemmed Evolutionary autonomous agents and the nature of apraxia
title_short Evolutionary autonomous agents and the nature of apraxia
title_sort evolutionary autonomous agents and the nature of apraxia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC544844/
https://www.ncbi.nlm.nih.gov/pubmed/15631635
http://dx.doi.org/10.1186/1475-925X-4-1
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