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A cholinergic feedback circuit to regulate striatal population uncertainty and optimize reinforcement learning
Convergent evidence suggests that the basal ganglia support reinforcement learning by adjusting action values according to reward prediction errors. However, adaptive behavior in stochastic environments requires the consideration of uncertainty to dynamically adjust the learning rate. We consider ho...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764588/ https://www.ncbi.nlm.nih.gov/pubmed/26705698 http://dx.doi.org/10.7554/eLife.12029 |
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author | Franklin, Nicholas T Frank, Michael J |
author_facet | Franklin, Nicholas T Frank, Michael J |
author_sort | Franklin, Nicholas T |
collection | PubMed |
description | Convergent evidence suggests that the basal ganglia support reinforcement learning by adjusting action values according to reward prediction errors. However, adaptive behavior in stochastic environments requires the consideration of uncertainty to dynamically adjust the learning rate. We consider how cholinergic tonically active interneurons (TANs) may endow the striatum with such a mechanism in computational models spanning three Marr's levels of analysis. In the neural model, TANs modulate the excitability of spiny neurons, their population response to reinforcement, and hence the effective learning rate. Long TAN pauses facilitated robustness to spurious outcomes by increasing divergence in synaptic weights between neurons coding for alternative action values, whereas short TAN pauses facilitated stochastic behavior but increased responsiveness to change-points in outcome contingencies. A feedback control system allowed TAN pauses to be dynamically modulated by uncertainty across the spiny neuron population, allowing the system to self-tune and optimize performance across stochastic environments. DOI: http://dx.doi.org/10.7554/eLife.12029.001 |
format | Online Article Text |
id | pubmed-4764588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47645882016-02-25 A cholinergic feedback circuit to regulate striatal population uncertainty and optimize reinforcement learning Franklin, Nicholas T Frank, Michael J eLife Computational and Systems Biology Convergent evidence suggests that the basal ganglia support reinforcement learning by adjusting action values according to reward prediction errors. However, adaptive behavior in stochastic environments requires the consideration of uncertainty to dynamically adjust the learning rate. We consider how cholinergic tonically active interneurons (TANs) may endow the striatum with such a mechanism in computational models spanning three Marr's levels of analysis. In the neural model, TANs modulate the excitability of spiny neurons, their population response to reinforcement, and hence the effective learning rate. Long TAN pauses facilitated robustness to spurious outcomes by increasing divergence in synaptic weights between neurons coding for alternative action values, whereas short TAN pauses facilitated stochastic behavior but increased responsiveness to change-points in outcome contingencies. A feedback control system allowed TAN pauses to be dynamically modulated by uncertainty across the spiny neuron population, allowing the system to self-tune and optimize performance across stochastic environments. DOI: http://dx.doi.org/10.7554/eLife.12029.001 eLife Sciences Publications, Ltd 2015-12-25 /pmc/articles/PMC4764588/ /pubmed/26705698 http://dx.doi.org/10.7554/eLife.12029 Text en © 2015, Franklin et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Franklin, Nicholas T Frank, Michael J A cholinergic feedback circuit to regulate striatal population uncertainty and optimize reinforcement learning |
title | A cholinergic feedback circuit to regulate striatal population uncertainty and optimize reinforcement learning |
title_full | A cholinergic feedback circuit to regulate striatal population uncertainty and optimize reinforcement learning |
title_fullStr | A cholinergic feedback circuit to regulate striatal population uncertainty and optimize reinforcement learning |
title_full_unstemmed | A cholinergic feedback circuit to regulate striatal population uncertainty and optimize reinforcement learning |
title_short | A cholinergic feedback circuit to regulate striatal population uncertainty and optimize reinforcement learning |
title_sort | cholinergic feedback circuit to regulate striatal population uncertainty and optimize reinforcement learning |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764588/ https://www.ncbi.nlm.nih.gov/pubmed/26705698 http://dx.doi.org/10.7554/eLife.12029 |
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