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Exploration behavior after reversals is predicted by STN-GPe synaptic plasticity in a basal ganglia model

Humans can quickly adapt their behavior to changes in the environment. Classical reversal learning tasks mainly measure how well participants can disengage from a previously successful behavior but not how alternative responses are explored. Here, we propose a novel 5-choice reversal learning task w...

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Detalles Bibliográficos
Autores principales: Maith, Oliver, Baladron, Javier, Einhäuser, Wolfgang, Hamker, Fred H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214406/
https://www.ncbi.nlm.nih.gov/pubmed/37250300
http://dx.doi.org/10.1016/j.isci.2023.106599
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author Maith, Oliver
Baladron, Javier
Einhäuser, Wolfgang
Hamker, Fred H.
author_facet Maith, Oliver
Baladron, Javier
Einhäuser, Wolfgang
Hamker, Fred H.
author_sort Maith, Oliver
collection PubMed
description Humans can quickly adapt their behavior to changes in the environment. Classical reversal learning tasks mainly measure how well participants can disengage from a previously successful behavior but not how alternative responses are explored. Here, we propose a novel 5-choice reversal learning task with alternating position-reward contingencies to study exploration behavior after a reversal. We compare human exploratory saccade behavior with a prediction obtained from a neuro-computational model of the basal ganglia. A new synaptic plasticity rule for learning the connectivity between the subthalamic nucleus (STN) and external globus pallidus (GPe) results in exploration biases to previously rewarded positions. The model simulations and human data both show that during experimental experience exploration becomes limited to only those positions that have been rewarded in the past. Our study demonstrates how quite complex behavior may result from a simple sub-circuit within the basal ganglia pathways.
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spelling pubmed-102144062023-05-27 Exploration behavior after reversals is predicted by STN-GPe synaptic plasticity in a basal ganglia model Maith, Oliver Baladron, Javier Einhäuser, Wolfgang Hamker, Fred H. iScience Article Humans can quickly adapt their behavior to changes in the environment. Classical reversal learning tasks mainly measure how well participants can disengage from a previously successful behavior but not how alternative responses are explored. Here, we propose a novel 5-choice reversal learning task with alternating position-reward contingencies to study exploration behavior after a reversal. We compare human exploratory saccade behavior with a prediction obtained from a neuro-computational model of the basal ganglia. A new synaptic plasticity rule for learning the connectivity between the subthalamic nucleus (STN) and external globus pallidus (GPe) results in exploration biases to previously rewarded positions. The model simulations and human data both show that during experimental experience exploration becomes limited to only those positions that have been rewarded in the past. Our study demonstrates how quite complex behavior may result from a simple sub-circuit within the basal ganglia pathways. Elsevier 2023-04-11 /pmc/articles/PMC10214406/ /pubmed/37250300 http://dx.doi.org/10.1016/j.isci.2023.106599 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Maith, Oliver
Baladron, Javier
Einhäuser, Wolfgang
Hamker, Fred H.
Exploration behavior after reversals is predicted by STN-GPe synaptic plasticity in a basal ganglia model
title Exploration behavior after reversals is predicted by STN-GPe synaptic plasticity in a basal ganglia model
title_full Exploration behavior after reversals is predicted by STN-GPe synaptic plasticity in a basal ganglia model
title_fullStr Exploration behavior after reversals is predicted by STN-GPe synaptic plasticity in a basal ganglia model
title_full_unstemmed Exploration behavior after reversals is predicted by STN-GPe synaptic plasticity in a basal ganglia model
title_short Exploration behavior after reversals is predicted by STN-GPe synaptic plasticity in a basal ganglia model
title_sort exploration behavior after reversals is predicted by stn-gpe synaptic plasticity in a basal ganglia model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214406/
https://www.ncbi.nlm.nih.gov/pubmed/37250300
http://dx.doi.org/10.1016/j.isci.2023.106599
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