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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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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. |
format | Online Article Text |
id | pubmed-10025386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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