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Development of Mechanistic Neural Mass (mNM) Models that Link Physiology to Mean-Field Dynamics

Brain rhythms emerge from the mean-field activity of networks of neurons. There have been many efforts to build mathematical and computational embodiments in the form of discrete cell-group activities—termed neural masses—to understand in particular the origins of evoked potentials, intrinsic patter...

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Detalles Bibliográficos
Autores principales: Tripathi, Richa, Gluckman, Bruce J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980379/
https://www.ncbi.nlm.nih.gov/pubmed/36876035
http://dx.doi.org/10.3389/fnetp.2022.911090
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author Tripathi, Richa
Gluckman, Bruce J.
author_facet Tripathi, Richa
Gluckman, Bruce J.
author_sort Tripathi, Richa
collection PubMed
description Brain rhythms emerge from the mean-field activity of networks of neurons. There have been many efforts to build mathematical and computational embodiments in the form of discrete cell-group activities—termed neural masses—to understand in particular the origins of evoked potentials, intrinsic patterns of activities such as theta, regulation of sleep, Parkinson’s disease related dynamics, and mimic seizure dynamics. As originally utilized, standard neural masses convert input through a sigmoidal function to a firing rate, and firing rate through a synaptic alpha function to other masses. Here we define a process to build mechanistic neural masses (mNMs) as mean-field models of microscopic membrane-type (Hodgkin Huxley type) models of different neuron types that duplicate the stability, firing rate, and associated bifurcations as function of relevant slow variables - such as extracellular potassium - and synaptic current; and whose output is both firing rate and impact on the slow variables - such as transmembrane potassium flux. Small networks composed of just excitatory and inhibitory mNMs demonstrate expected dynamical states including firing, runaway excitation and depolarization block, and these transitions change in biologically observed ways with changes in extracellular potassium and excitatory-inhibitory balance.
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spelling pubmed-99803792023-03-02 Development of Mechanistic Neural Mass (mNM) Models that Link Physiology to Mean-Field Dynamics Tripathi, Richa Gluckman, Bruce J. Front Netw Physiol Network Physiology Brain rhythms emerge from the mean-field activity of networks of neurons. There have been many efforts to build mathematical and computational embodiments in the form of discrete cell-group activities—termed neural masses—to understand in particular the origins of evoked potentials, intrinsic patterns of activities such as theta, regulation of sleep, Parkinson’s disease related dynamics, and mimic seizure dynamics. As originally utilized, standard neural masses convert input through a sigmoidal function to a firing rate, and firing rate through a synaptic alpha function to other masses. Here we define a process to build mechanistic neural masses (mNMs) as mean-field models of microscopic membrane-type (Hodgkin Huxley type) models of different neuron types that duplicate the stability, firing rate, and associated bifurcations as function of relevant slow variables - such as extracellular potassium - and synaptic current; and whose output is both firing rate and impact on the slow variables - such as transmembrane potassium flux. Small networks composed of just excitatory and inhibitory mNMs demonstrate expected dynamical states including firing, runaway excitation and depolarization block, and these transitions change in biologically observed ways with changes in extracellular potassium and excitatory-inhibitory balance. Frontiers Media S.A. 2022-09-28 /pmc/articles/PMC9980379/ /pubmed/36876035 http://dx.doi.org/10.3389/fnetp.2022.911090 Text en Copyright © 2022 Tripathi and Gluckman. 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 Network Physiology
Tripathi, Richa
Gluckman, Bruce J.
Development of Mechanistic Neural Mass (mNM) Models that Link Physiology to Mean-Field Dynamics
title Development of Mechanistic Neural Mass (mNM) Models that Link Physiology to Mean-Field Dynamics
title_full Development of Mechanistic Neural Mass (mNM) Models that Link Physiology to Mean-Field Dynamics
title_fullStr Development of Mechanistic Neural Mass (mNM) Models that Link Physiology to Mean-Field Dynamics
title_full_unstemmed Development of Mechanistic Neural Mass (mNM) Models that Link Physiology to Mean-Field Dynamics
title_short Development of Mechanistic Neural Mass (mNM) Models that Link Physiology to Mean-Field Dynamics
title_sort development of mechanistic neural mass (mnm) models that link physiology to mean-field dynamics
topic Network Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980379/
https://www.ncbi.nlm.nih.gov/pubmed/36876035
http://dx.doi.org/10.3389/fnetp.2022.911090
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