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Reward-driven changes in striatal pathway competition shape evidence evaluation in decision-making

Cortico-basal-ganglia-thalamic (CBGT) networks are critical for adaptive decision-making, yet how changes to circuit-level properties impact cognitive algorithms remains unclear. Here we explore how dopaminergic plasticity at corticostriatal synapses alters competition between striatal pathways, imp...

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Autores principales: Dunovan, Kyle, Vich, Catalina, Clapp, Matthew, Verstynen, Timothy, Rubin, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534331/
https://www.ncbi.nlm.nih.gov/pubmed/31060045
http://dx.doi.org/10.1371/journal.pcbi.1006998
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author Dunovan, Kyle
Vich, Catalina
Clapp, Matthew
Verstynen, Timothy
Rubin, Jonathan
author_facet Dunovan, Kyle
Vich, Catalina
Clapp, Matthew
Verstynen, Timothy
Rubin, Jonathan
author_sort Dunovan, Kyle
collection PubMed
description Cortico-basal-ganglia-thalamic (CBGT) networks are critical for adaptive decision-making, yet how changes to circuit-level properties impact cognitive algorithms remains unclear. Here we explore how dopaminergic plasticity at corticostriatal synapses alters competition between striatal pathways, impacting the evidence accumulation process during decision-making. Spike-timing dependent plasticity simulations showed that dopaminergic feedback based on rewards modified the ratio of direct and indirect corticostriatal weights within opposing action channels. Using the learned weight ratios in a full spiking CBGT network model, we simulated neural dynamics and decision outcomes in a reward-driven decision task and fit them with a drift diffusion model. Fits revealed that the rate of evidence accumulation varied with inter-channel differences in direct pathway activity while boundary height varied with overall indirect pathway activity. This multi-level modeling approach demonstrates how complementary learning and decision computations can emerge from corticostriatal plasticity.
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spelling pubmed-65343312019-06-05 Reward-driven changes in striatal pathway competition shape evidence evaluation in decision-making Dunovan, Kyle Vich, Catalina Clapp, Matthew Verstynen, Timothy Rubin, Jonathan PLoS Comput Biol Research Article Cortico-basal-ganglia-thalamic (CBGT) networks are critical for adaptive decision-making, yet how changes to circuit-level properties impact cognitive algorithms remains unclear. Here we explore how dopaminergic plasticity at corticostriatal synapses alters competition between striatal pathways, impacting the evidence accumulation process during decision-making. Spike-timing dependent plasticity simulations showed that dopaminergic feedback based on rewards modified the ratio of direct and indirect corticostriatal weights within opposing action channels. Using the learned weight ratios in a full spiking CBGT network model, we simulated neural dynamics and decision outcomes in a reward-driven decision task and fit them with a drift diffusion model. Fits revealed that the rate of evidence accumulation varied with inter-channel differences in direct pathway activity while boundary height varied with overall indirect pathway activity. This multi-level modeling approach demonstrates how complementary learning and decision computations can emerge from corticostriatal plasticity. Public Library of Science 2019-05-06 /pmc/articles/PMC6534331/ /pubmed/31060045 http://dx.doi.org/10.1371/journal.pcbi.1006998 Text en © 2019 Dunovan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dunovan, Kyle
Vich, Catalina
Clapp, Matthew
Verstynen, Timothy
Rubin, Jonathan
Reward-driven changes in striatal pathway competition shape evidence evaluation in decision-making
title Reward-driven changes in striatal pathway competition shape evidence evaluation in decision-making
title_full Reward-driven changes in striatal pathway competition shape evidence evaluation in decision-making
title_fullStr Reward-driven changes in striatal pathway competition shape evidence evaluation in decision-making
title_full_unstemmed Reward-driven changes in striatal pathway competition shape evidence evaluation in decision-making
title_short Reward-driven changes in striatal pathway competition shape evidence evaluation in decision-making
title_sort reward-driven changes in striatal pathway competition shape evidence evaluation in decision-making
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534331/
https://www.ncbi.nlm.nih.gov/pubmed/31060045
http://dx.doi.org/10.1371/journal.pcbi.1006998
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