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A computational passage-of-time model of the cerebellar Purkinje cell in eyeblink conditioning

The cerebellar Purkinje cell controlling eyeblinks can learn, remember, and reproduce the interstimulus interval in a classical conditioning paradigm. Given temporally separated inputs, the cerebellar Purkinje cell learns to pause its tonic inhibition of a motor pathway with high temporal precision...

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Detalles Bibliográficos
Autores principales: Ricci, Matthew, Kim, Junkyung, Johansson, Fredrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025386/
https://www.ncbi.nlm.nih.gov/pubmed/36950506
http://dx.doi.org/10.3389/fncom.2023.1108346
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author Ricci, Matthew
Kim, Junkyung
Johansson, Fredrik
author_facet Ricci, Matthew
Kim, Junkyung
Johansson, Fredrik
author_sort Ricci, Matthew
collection PubMed
description The cerebellar Purkinje cell controlling eyeblinks can learn, remember, and reproduce the interstimulus interval in a classical conditioning paradigm. Given temporally separated inputs, the cerebellar Purkinje cell learns to pause its tonic inhibition of a motor pathway with high temporal precision so that an overt blink occurs at the right time. Most models place the passage-of-time representation in upstream network effects. Yet, bypassing the upstream network and directly stimulating the Purkinje cell's pre-synaptic fibers during conditioning still causes acquisition of a well-timed response. Additionally, while network models are sensitive to variance in the temporal structure of probe stimulation, in vivo findings suggest that the acquired Purkinje cell response is not. Such findings motivate alternative approaches to modeling neural function. Here, we present a proof-of-principle model of the passage-of-time which is internal to the Purkinje cell and is invariant to probe structure. The model is consistent with puzzling findings, accurately recapitulates Purkinje cell firing during classical conditioning and makes testable electrophysiological predictions.
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spelling pubmed-100253862023-03-21 A computational passage-of-time model of the cerebellar Purkinje cell in eyeblink conditioning Ricci, Matthew Kim, Junkyung Johansson, Fredrik Front Comput Neurosci Neuroscience The cerebellar Purkinje cell controlling eyeblinks can learn, remember, and reproduce the interstimulus interval in a classical conditioning paradigm. Given temporally separated inputs, the cerebellar Purkinje cell learns to pause its tonic inhibition of a motor pathway with high temporal precision so that an overt blink occurs at the right time. Most models place the passage-of-time representation in upstream network effects. Yet, bypassing the upstream network and directly stimulating the Purkinje cell's pre-synaptic fibers during conditioning still causes acquisition of a well-timed response. Additionally, while network models are sensitive to variance in the temporal structure of probe stimulation, in vivo findings suggest that the acquired Purkinje cell response is not. Such findings motivate alternative approaches to modeling neural function. Here, we present a proof-of-principle model of the passage-of-time which is internal to the Purkinje cell and is invariant to probe structure. The model is consistent with puzzling findings, accurately recapitulates Purkinje cell firing during classical conditioning and makes testable electrophysiological predictions. Frontiers Media S.A. 2023-03-06 /pmc/articles/PMC10025386/ /pubmed/36950506 http://dx.doi.org/10.3389/fncom.2023.1108346 Text en Copyright © 2023 Ricci, Kim and Johansson. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Ricci, Matthew
Kim, Junkyung
Johansson, Fredrik
A computational passage-of-time model of the cerebellar Purkinje cell in eyeblink conditioning
title A computational passage-of-time model of the cerebellar Purkinje cell in eyeblink conditioning
title_full A computational passage-of-time model of the cerebellar Purkinje cell in eyeblink conditioning
title_fullStr A computational passage-of-time model of the cerebellar Purkinje cell in eyeblink conditioning
title_full_unstemmed A computational passage-of-time model of the cerebellar Purkinje cell in eyeblink conditioning
title_short A computational passage-of-time model of the cerebellar Purkinje cell in eyeblink conditioning
title_sort computational passage-of-time model of the cerebellar purkinje cell in eyeblink conditioning
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025386/
https://www.ncbi.nlm.nih.gov/pubmed/36950506
http://dx.doi.org/10.3389/fncom.2023.1108346
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