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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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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. |
format | Online Article Text |
id | pubmed-10214406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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