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Acetylcholine-Based Entropy in Response Selection: A Model of How Striatal Interneurons Modulate Exploration, Exploitation, and Response Variability in Decision-Making
The basal ganglia play a fundamental role in decision-making. Their contribution is typically modeled within a reinforcement learning framework, with the basal ganglia learning to select the options associated with highest value and their dopamine inputs conveying performance feedback. This basic fr...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Research Foundation
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3272653/ https://www.ncbi.nlm.nih.gov/pubmed/22347164 http://dx.doi.org/10.3389/fnins.2012.00018 |
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author | Stocco, Andrea |
author_facet | Stocco, Andrea |
author_sort | Stocco, Andrea |
collection | PubMed |
description | The basal ganglia play a fundamental role in decision-making. Their contribution is typically modeled within a reinforcement learning framework, with the basal ganglia learning to select the options associated with highest value and their dopamine inputs conveying performance feedback. This basic framework, however, does not account for the role of cholinergic interneurons in the striatum, and does not easily explain certain dynamic aspects of decision-making and skill acquisition like the generation of exploratory actions. This paper describes basal ganglia acetylcholine-based entropy (BABE), a model of the acetylcholine system in the striatum that provides a unified explanation for these phenomena. According to this model, cholinergic interneurons in the striatum control the level of variability in behavior by modulating the number of possible responses that are considered by the basal ganglia, as well as the level of competition between them. This mechanism provides a natural way to account for the role of basal ganglia in generating behavioral variability during the acquisition of certain cognitive skills, as well as for modulating exploration and exploitation in decision-making. Compared to a typical reinforcement learning model, BABE showed a greater modulation of response variability in the face of changes in the reward contingences, allowing for faster learning (and re-learning) of option values. Finally, the paper discusses the possible applications of the model to other domains. |
format | Online Article Text |
id | pubmed-3272653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32726532012-02-15 Acetylcholine-Based Entropy in Response Selection: A Model of How Striatal Interneurons Modulate Exploration, Exploitation, and Response Variability in Decision-Making Stocco, Andrea Front Neurosci Neuroscience The basal ganglia play a fundamental role in decision-making. Their contribution is typically modeled within a reinforcement learning framework, with the basal ganglia learning to select the options associated with highest value and their dopamine inputs conveying performance feedback. This basic framework, however, does not account for the role of cholinergic interneurons in the striatum, and does not easily explain certain dynamic aspects of decision-making and skill acquisition like the generation of exploratory actions. This paper describes basal ganglia acetylcholine-based entropy (BABE), a model of the acetylcholine system in the striatum that provides a unified explanation for these phenomena. According to this model, cholinergic interneurons in the striatum control the level of variability in behavior by modulating the number of possible responses that are considered by the basal ganglia, as well as the level of competition between them. This mechanism provides a natural way to account for the role of basal ganglia in generating behavioral variability during the acquisition of certain cognitive skills, as well as for modulating exploration and exploitation in decision-making. Compared to a typical reinforcement learning model, BABE showed a greater modulation of response variability in the face of changes in the reward contingences, allowing for faster learning (and re-learning) of option values. Finally, the paper discusses the possible applications of the model to other domains. Frontiers Research Foundation 2012-02-06 /pmc/articles/PMC3272653/ /pubmed/22347164 http://dx.doi.org/10.3389/fnins.2012.00018 Text en Copyright © 2012 Stocco. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Neuroscience Stocco, Andrea Acetylcholine-Based Entropy in Response Selection: A Model of How Striatal Interneurons Modulate Exploration, Exploitation, and Response Variability in Decision-Making |
title | Acetylcholine-Based Entropy in Response Selection: A Model of How Striatal Interneurons Modulate Exploration, Exploitation, and Response Variability in Decision-Making |
title_full | Acetylcholine-Based Entropy in Response Selection: A Model of How Striatal Interneurons Modulate Exploration, Exploitation, and Response Variability in Decision-Making |
title_fullStr | Acetylcholine-Based Entropy in Response Selection: A Model of How Striatal Interneurons Modulate Exploration, Exploitation, and Response Variability in Decision-Making |
title_full_unstemmed | Acetylcholine-Based Entropy in Response Selection: A Model of How Striatal Interneurons Modulate Exploration, Exploitation, and Response Variability in Decision-Making |
title_short | Acetylcholine-Based Entropy in Response Selection: A Model of How Striatal Interneurons Modulate Exploration, Exploitation, and Response Variability in Decision-Making |
title_sort | acetylcholine-based entropy in response selection: a model of how striatal interneurons modulate exploration, exploitation, and response variability in decision-making |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3272653/ https://www.ncbi.nlm.nih.gov/pubmed/22347164 http://dx.doi.org/10.3389/fnins.2012.00018 |
work_keys_str_mv | AT stoccoandrea acetylcholinebasedentropyinresponseselectionamodelofhowstriatalinterneuronsmodulateexplorationexploitationandresponsevariabilityindecisionmaking |