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Biophysical modeling of frontocentral ERP generation links circuit-level mechanisms of action-stopping to a behavioral race model
Human frontocentral event-related potentials (FC-ERPs) are ubiquitous neural correlates of cognition and control, but their generating multiscale mechanisms remain mostly unknown. We used the Human Neocortical Neurosolver(HNN)’s biophysical model of a canonical neocortical circuit under exogenous th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634895/ https://www.ncbi.nlm.nih.gov/pubmed/37961333 http://dx.doi.org/10.1101/2023.10.25.564020 |
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author | Diesburg, Darcy A. Wessel, Jan R. Jones, Stephanie R. |
author_facet | Diesburg, Darcy A. Wessel, Jan R. Jones, Stephanie R. |
author_sort | Diesburg, Darcy A. |
collection | PubMed |
description | Human frontocentral event-related potentials (FC-ERPs) are ubiquitous neural correlates of cognition and control, but their generating multiscale mechanisms remain mostly unknown. We used the Human Neocortical Neurosolver(HNN)’s biophysical model of a canonical neocortical circuit under exogenous thalamic and cortical drive to simulate the cell and circuit mechanisms underpinning the P2, N2, and P3 features of the FC-ERP observed after Stop-Signals in the Stop-Signal task (SST). We demonstrate that a sequence of simulated external thalamocortical and cortico-cortical drives can produce the FC-ERP, similar to what has been shown for primary sensory cortices. We used this model of the FC-ERP to examine likely circuit-mechanisms underlying FC-ERP features that distinguish between successful and failed action-stopping. We also tested their adherence to the predictions of the horse-race model of the SST, with specific hypotheses motivated by theoretical links between the P3 and Stop process. These simulations revealed that a difference in P3 onset between successful and failed Stops is most likely due to a later arrival of thalamocortical drive in failed Stops, rather than, for example, a difference in effective strength of the input. In contrast, the same model predicted that early thalamocortical drives underpinning the P2 and N2 differed in both strength and timing across stopping accuracy conditions. Overall, this model generates novel testable predictions of the thalamocortical dynamics underlying FC-ERP generation during action-stopping. Moreover, it provides a detailed cellular and circuit-level interpretation that supports links between these macroscale signatures and predictions of the behavioral race model. |
format | Online Article Text |
id | pubmed-10634895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106348952023-11-13 Biophysical modeling of frontocentral ERP generation links circuit-level mechanisms of action-stopping to a behavioral race model Diesburg, Darcy A. Wessel, Jan R. Jones, Stephanie R. bioRxiv Article Human frontocentral event-related potentials (FC-ERPs) are ubiquitous neural correlates of cognition and control, but their generating multiscale mechanisms remain mostly unknown. We used the Human Neocortical Neurosolver(HNN)’s biophysical model of a canonical neocortical circuit under exogenous thalamic and cortical drive to simulate the cell and circuit mechanisms underpinning the P2, N2, and P3 features of the FC-ERP observed after Stop-Signals in the Stop-Signal task (SST). We demonstrate that a sequence of simulated external thalamocortical and cortico-cortical drives can produce the FC-ERP, similar to what has been shown for primary sensory cortices. We used this model of the FC-ERP to examine likely circuit-mechanisms underlying FC-ERP features that distinguish between successful and failed action-stopping. We also tested their adherence to the predictions of the horse-race model of the SST, with specific hypotheses motivated by theoretical links between the P3 and Stop process. These simulations revealed that a difference in P3 onset between successful and failed Stops is most likely due to a later arrival of thalamocortical drive in failed Stops, rather than, for example, a difference in effective strength of the input. In contrast, the same model predicted that early thalamocortical drives underpinning the P2 and N2 differed in both strength and timing across stopping accuracy conditions. Overall, this model generates novel testable predictions of the thalamocortical dynamics underlying FC-ERP generation during action-stopping. Moreover, it provides a detailed cellular and circuit-level interpretation that supports links between these macroscale signatures and predictions of the behavioral race model. Cold Spring Harbor Laboratory 2023-10-30 /pmc/articles/PMC10634895/ /pubmed/37961333 http://dx.doi.org/10.1101/2023.10.25.564020 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Diesburg, Darcy A. Wessel, Jan R. Jones, Stephanie R. Biophysical modeling of frontocentral ERP generation links circuit-level mechanisms of action-stopping to a behavioral race model |
title | Biophysical modeling of frontocentral ERP generation links circuit-level mechanisms of action-stopping to a behavioral race model |
title_full | Biophysical modeling of frontocentral ERP generation links circuit-level mechanisms of action-stopping to a behavioral race model |
title_fullStr | Biophysical modeling of frontocentral ERP generation links circuit-level mechanisms of action-stopping to a behavioral race model |
title_full_unstemmed | Biophysical modeling of frontocentral ERP generation links circuit-level mechanisms of action-stopping to a behavioral race model |
title_short | Biophysical modeling of frontocentral ERP generation links circuit-level mechanisms of action-stopping to a behavioral race model |
title_sort | biophysical modeling of frontocentral erp generation links circuit-level mechanisms of action-stopping to a behavioral race model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634895/ https://www.ncbi.nlm.nih.gov/pubmed/37961333 http://dx.doi.org/10.1101/2023.10.25.564020 |
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