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Emergence of time persistence in a data-driven neural network model

Establishing accurate as well as interpretable models of network activity is an open challenge in systems neuroscience. Here, we infer an energy-based model of the anterior rhombencephalic turning region (ARTR), a circuit that controls zebrafish swimming statistics, using functional recordings of th...

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Autores principales: Wolf, Sebastien, Le Goc, Guillaume, Debrégeas, Georges, Cocco, Simona, Monasson, Rémi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171858/
https://www.ncbi.nlm.nih.gov/pubmed/36916902
http://dx.doi.org/10.7554/eLife.79541
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author Wolf, Sebastien
Le Goc, Guillaume
Debrégeas, Georges
Cocco, Simona
Monasson, Rémi
author_facet Wolf, Sebastien
Le Goc, Guillaume
Debrégeas, Georges
Cocco, Simona
Monasson, Rémi
author_sort Wolf, Sebastien
collection PubMed
description Establishing accurate as well as interpretable models of network activity is an open challenge in systems neuroscience. Here, we infer an energy-based model of the anterior rhombencephalic turning region (ARTR), a circuit that controls zebrafish swimming statistics, using functional recordings of the spontaneous activity of hundreds of neurons. Although our model is trained to reproduce the low-order statistics of the network activity at short time scales, its simulated dynamics quantitatively captures the slowly alternating activity of the ARTR. It further reproduces the modulation of this persistent dynamics by the water temperature and visual stimulation. Mathematical analysis of the model unveils a low-dimensional landscape-based representation of the ARTR activity, where the slow network dynamics reflects Arrhenius-like barriers crossings between metastable states. Our work thus shows how data-driven models built from large neural populations recordings can be reduced to low-dimensional functional models in order to reveal the fundamental mechanisms controlling the collective neuronal dynamics.
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spelling pubmed-101718582023-05-11 Emergence of time persistence in a data-driven neural network model Wolf, Sebastien Le Goc, Guillaume Debrégeas, Georges Cocco, Simona Monasson, Rémi eLife Neuroscience Establishing accurate as well as interpretable models of network activity is an open challenge in systems neuroscience. Here, we infer an energy-based model of the anterior rhombencephalic turning region (ARTR), a circuit that controls zebrafish swimming statistics, using functional recordings of the spontaneous activity of hundreds of neurons. Although our model is trained to reproduce the low-order statistics of the network activity at short time scales, its simulated dynamics quantitatively captures the slowly alternating activity of the ARTR. It further reproduces the modulation of this persistent dynamics by the water temperature and visual stimulation. Mathematical analysis of the model unveils a low-dimensional landscape-based representation of the ARTR activity, where the slow network dynamics reflects Arrhenius-like barriers crossings between metastable states. Our work thus shows how data-driven models built from large neural populations recordings can be reduced to low-dimensional functional models in order to reveal the fundamental mechanisms controlling the collective neuronal dynamics. eLife Sciences Publications, Ltd 2023-03-14 /pmc/articles/PMC10171858/ /pubmed/36916902 http://dx.doi.org/10.7554/eLife.79541 Text en © 2023, Wolf, Le Goc, Debrégeas et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Wolf, Sebastien
Le Goc, Guillaume
Debrégeas, Georges
Cocco, Simona
Monasson, Rémi
Emergence of time persistence in a data-driven neural network model
title Emergence of time persistence in a data-driven neural network model
title_full Emergence of time persistence in a data-driven neural network model
title_fullStr Emergence of time persistence in a data-driven neural network model
title_full_unstemmed Emergence of time persistence in a data-driven neural network model
title_short Emergence of time persistence in a data-driven neural network model
title_sort emergence of time persistence in a data-driven neural network model
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171858/
https://www.ncbi.nlm.nih.gov/pubmed/36916902
http://dx.doi.org/10.7554/eLife.79541
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