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Cross-scale excitability in networks of quadratic integrate-and-fire neurons
From the action potentials of neurons and cardiac cells to the amplification of calcium signals in oocytes, excitability is a hallmark of many biological signalling processes. In recent years, excitability in single cells has been related to multiple-timescale dynamics through canards, special solut...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560555/ https://www.ncbi.nlm.nih.gov/pubmed/36191049 http://dx.doi.org/10.1371/journal.pcbi.1010569 |
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author | Avitabile, Daniele Desroches, Mathieu Ermentrout, G. Bard |
author_facet | Avitabile, Daniele Desroches, Mathieu Ermentrout, G. Bard |
author_sort | Avitabile, Daniele |
collection | PubMed |
description | From the action potentials of neurons and cardiac cells to the amplification of calcium signals in oocytes, excitability is a hallmark of many biological signalling processes. In recent years, excitability in single cells has been related to multiple-timescale dynamics through canards, special solutions which determine the effective thresholds of the all-or-none responses. However, the emergence of excitability in large populations remains an open problem. Here, we show that the mechanism of excitability in large networks and mean-field descriptions of coupled quadratic integrate-and-fire (QIF) cells mirrors that of the individual components. We initially exploit the Ott-Antonsen ansatz to derive low-dimensional dynamics for the coupled network and use it to describe the structure of canards via slow periodic forcing. We demonstrate that the thresholds for onset and offset of population firing can be found in the same way as those of the single cell. We combine theoretical analysis and numerical computations to develop a novel and comprehensive framework for excitability in large populations, applicable not only to models amenable to Ott-Antonsen reduction, but also to networks without a closed-form mean-field limit, in particular sparse networks. |
format | Online Article Text |
id | pubmed-9560555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-95605552022-10-14 Cross-scale excitability in networks of quadratic integrate-and-fire neurons Avitabile, Daniele Desroches, Mathieu Ermentrout, G. Bard PLoS Comput Biol Research Article From the action potentials of neurons and cardiac cells to the amplification of calcium signals in oocytes, excitability is a hallmark of many biological signalling processes. In recent years, excitability in single cells has been related to multiple-timescale dynamics through canards, special solutions which determine the effective thresholds of the all-or-none responses. However, the emergence of excitability in large populations remains an open problem. Here, we show that the mechanism of excitability in large networks and mean-field descriptions of coupled quadratic integrate-and-fire (QIF) cells mirrors that of the individual components. We initially exploit the Ott-Antonsen ansatz to derive low-dimensional dynamics for the coupled network and use it to describe the structure of canards via slow periodic forcing. We demonstrate that the thresholds for onset and offset of population firing can be found in the same way as those of the single cell. We combine theoretical analysis and numerical computations to develop a novel and comprehensive framework for excitability in large populations, applicable not only to models amenable to Ott-Antonsen reduction, but also to networks without a closed-form mean-field limit, in particular sparse networks. Public Library of Science 2022-10-03 /pmc/articles/PMC9560555/ /pubmed/36191049 http://dx.doi.org/10.1371/journal.pcbi.1010569 Text en © 2022 Avitabile et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Avitabile, Daniele Desroches, Mathieu Ermentrout, G. Bard Cross-scale excitability in networks of quadratic integrate-and-fire neurons |
title | Cross-scale excitability in networks of quadratic integrate-and-fire neurons |
title_full | Cross-scale excitability in networks of quadratic integrate-and-fire neurons |
title_fullStr | Cross-scale excitability in networks of quadratic integrate-and-fire neurons |
title_full_unstemmed | Cross-scale excitability in networks of quadratic integrate-and-fire neurons |
title_short | Cross-scale excitability in networks of quadratic integrate-and-fire neurons |
title_sort | cross-scale excitability in networks of quadratic integrate-and-fire neurons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560555/ https://www.ncbi.nlm.nih.gov/pubmed/36191049 http://dx.doi.org/10.1371/journal.pcbi.1010569 |
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