Cargando…

A neurocomputational theory of how explicit learning bootstraps early procedural learning

It is widely accepted that human learning and memory is mediated by multiple memory systems that are each best suited to different requirements and demands. Within the domain of categorization, at least two systems are thought to facilitate learning: an explicit (declarative) system depending largel...

Descripción completa

Detalles Bibliográficos
Autores principales: Paul, Erick J., Ashby, F. Gregory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866519/
https://www.ncbi.nlm.nih.gov/pubmed/24385962
http://dx.doi.org/10.3389/fncom.2013.00177
_version_ 1782296171441553408
author Paul, Erick J.
Ashby, F. Gregory
author_facet Paul, Erick J.
Ashby, F. Gregory
author_sort Paul, Erick J.
collection PubMed
description It is widely accepted that human learning and memory is mediated by multiple memory systems that are each best suited to different requirements and demands. Within the domain of categorization, at least two systems are thought to facilitate learning: an explicit (declarative) system depending largely on the prefrontal cortex, and a procedural (non-declarative) system depending on the basal ganglia. Substantial evidence suggests that each system is optimally suited to learn particular categorization tasks. However, it remains unknown precisely how these systems interact to produce optimal learning and behavior. In order to investigate this issue, the present research evaluated the progression of learning through simulation of categorization tasks using COVIS, a well-known model of human category learning that includes both explicit and procedural learning systems. Specifically, the model's parameter space was thoroughly explored in procedurally learned categorization tasks across a variety of conditions and architectures to identify plausible interaction architectures. The simulation results support the hypothesis that one-way interaction between the systems occurs such that the explicit system “bootstraps” learning early on in the procedural system. Thus, the procedural system initially learns a suboptimal strategy employed by the explicit system and later refines its strategy. This bootstrapping could be from cortical-striatal projections that originate in premotor or motor regions of cortex, or possibly by the explicit system's control of motor responses through basal ganglia-mediated loops
format Online
Article
Text
id pubmed-3866519
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-38665192014-01-02 A neurocomputational theory of how explicit learning bootstraps early procedural learning Paul, Erick J. Ashby, F. Gregory Front Comput Neurosci Neuroscience It is widely accepted that human learning and memory is mediated by multiple memory systems that are each best suited to different requirements and demands. Within the domain of categorization, at least two systems are thought to facilitate learning: an explicit (declarative) system depending largely on the prefrontal cortex, and a procedural (non-declarative) system depending on the basal ganglia. Substantial evidence suggests that each system is optimally suited to learn particular categorization tasks. However, it remains unknown precisely how these systems interact to produce optimal learning and behavior. In order to investigate this issue, the present research evaluated the progression of learning through simulation of categorization tasks using COVIS, a well-known model of human category learning that includes both explicit and procedural learning systems. Specifically, the model's parameter space was thoroughly explored in procedurally learned categorization tasks across a variety of conditions and architectures to identify plausible interaction architectures. The simulation results support the hypothesis that one-way interaction between the systems occurs such that the explicit system “bootstraps” learning early on in the procedural system. Thus, the procedural system initially learns a suboptimal strategy employed by the explicit system and later refines its strategy. This bootstrapping could be from cortical-striatal projections that originate in premotor or motor regions of cortex, or possibly by the explicit system's control of motor responses through basal ganglia-mediated loops Frontiers Media S.A. 2013-12-18 /pmc/articles/PMC3866519/ /pubmed/24385962 http://dx.doi.org/10.3389/fncom.2013.00177 Text en Copyright © 2013 Paul and Ashby. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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
Paul, Erick J.
Ashby, F. Gregory
A neurocomputational theory of how explicit learning bootstraps early procedural learning
title A neurocomputational theory of how explicit learning bootstraps early procedural learning
title_full A neurocomputational theory of how explicit learning bootstraps early procedural learning
title_fullStr A neurocomputational theory of how explicit learning bootstraps early procedural learning
title_full_unstemmed A neurocomputational theory of how explicit learning bootstraps early procedural learning
title_short A neurocomputational theory of how explicit learning bootstraps early procedural learning
title_sort neurocomputational theory of how explicit learning bootstraps early procedural learning
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866519/
https://www.ncbi.nlm.nih.gov/pubmed/24385962
http://dx.doi.org/10.3389/fncom.2013.00177
work_keys_str_mv AT paulerickj aneurocomputationaltheoryofhowexplicitlearningbootstrapsearlyprocedurallearning
AT ashbyfgregory aneurocomputationaltheoryofhowexplicitlearningbootstrapsearlyprocedurallearning
AT paulerickj neurocomputationaltheoryofhowexplicitlearningbootstrapsearlyprocedurallearning
AT ashbyfgregory neurocomputationaltheoryofhowexplicitlearningbootstrapsearlyprocedurallearning