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Comparison between an exact and a heuristic neural mass model with second-order synapses

Neural mass models (NMMs) are designed to reproduce the collective dynamics of neuronal populations. A common framework for NMMs assumes heuristically that the output firing rate of a neural population can be described by a static nonlinear transfer function (NMM1). However, a recent exact mean-fiel...

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Autores principales: Clusella, Pau, Köksal-Ersöz, Elif, Garcia-Ojalvo, Jordi, Ruffini, Giulio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160168/
https://www.ncbi.nlm.nih.gov/pubmed/36454267
http://dx.doi.org/10.1007/s00422-022-00952-7
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author Clusella, Pau
Köksal-Ersöz, Elif
Garcia-Ojalvo, Jordi
Ruffini, Giulio
author_facet Clusella, Pau
Köksal-Ersöz, Elif
Garcia-Ojalvo, Jordi
Ruffini, Giulio
author_sort Clusella, Pau
collection PubMed
description Neural mass models (NMMs) are designed to reproduce the collective dynamics of neuronal populations. A common framework for NMMs assumes heuristically that the output firing rate of a neural population can be described by a static nonlinear transfer function (NMM1). However, a recent exact mean-field theory for quadratic integrate-and-fire (QIF) neurons challenges this view by showing that the mean firing rate is not a static function of the neuronal state but follows two coupled nonlinear differential equations (NMM2). Here we analyze and compare these two descriptions in the presence of second-order synaptic dynamics. First, we derive the mathematical equivalence between the two models in the infinitely slow synapse limit, i.e., we show that NMM1 is an approximation of NMM2 in this regime. Next, we evaluate the applicability of this limit in the context of realistic physiological parameter values by analyzing the dynamics of models with inhibitory or excitatory synapses. We show that NMM1 fails to reproduce important dynamical features of the exact model, such as the self-sustained oscillations of an inhibitory interneuron QIF network. Furthermore, in the exact model but not in the limit one, stimulation of a pyramidal cell population induces resonant oscillatory activity whose peak frequency and amplitude increase with the self-coupling gain and the external excitatory input. This may play a role in the enhanced response of densely connected networks to weak uniform inputs, such as the electric fields produced by noninvasive brain stimulation.
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spelling pubmed-101601682023-05-06 Comparison between an exact and a heuristic neural mass model with second-order synapses Clusella, Pau Köksal-Ersöz, Elif Garcia-Ojalvo, Jordi Ruffini, Giulio Biol Cybern Original Article Neural mass models (NMMs) are designed to reproduce the collective dynamics of neuronal populations. A common framework for NMMs assumes heuristically that the output firing rate of a neural population can be described by a static nonlinear transfer function (NMM1). However, a recent exact mean-field theory for quadratic integrate-and-fire (QIF) neurons challenges this view by showing that the mean firing rate is not a static function of the neuronal state but follows two coupled nonlinear differential equations (NMM2). Here we analyze and compare these two descriptions in the presence of second-order synaptic dynamics. First, we derive the mathematical equivalence between the two models in the infinitely slow synapse limit, i.e., we show that NMM1 is an approximation of NMM2 in this regime. Next, we evaluate the applicability of this limit in the context of realistic physiological parameter values by analyzing the dynamics of models with inhibitory or excitatory synapses. We show that NMM1 fails to reproduce important dynamical features of the exact model, such as the self-sustained oscillations of an inhibitory interneuron QIF network. Furthermore, in the exact model but not in the limit one, stimulation of a pyramidal cell population induces resonant oscillatory activity whose peak frequency and amplitude increase with the self-coupling gain and the external excitatory input. This may play a role in the enhanced response of densely connected networks to weak uniform inputs, such as the electric fields produced by noninvasive brain stimulation. Springer Berlin Heidelberg 2022-12-01 2023 /pmc/articles/PMC10160168/ /pubmed/36454267 http://dx.doi.org/10.1007/s00422-022-00952-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Clusella, Pau
Köksal-Ersöz, Elif
Garcia-Ojalvo, Jordi
Ruffini, Giulio
Comparison between an exact and a heuristic neural mass model with second-order synapses
title Comparison between an exact and a heuristic neural mass model with second-order synapses
title_full Comparison between an exact and a heuristic neural mass model with second-order synapses
title_fullStr Comparison between an exact and a heuristic neural mass model with second-order synapses
title_full_unstemmed Comparison between an exact and a heuristic neural mass model with second-order synapses
title_short Comparison between an exact and a heuristic neural mass model with second-order synapses
title_sort comparison between an exact and a heuristic neural mass model with second-order synapses
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160168/
https://www.ncbi.nlm.nih.gov/pubmed/36454267
http://dx.doi.org/10.1007/s00422-022-00952-7
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