Synaptic Diversity Suppresses Complex Collective Behavior in Networks of Theta Neurons

Comprehending how the brain functions requires an understanding of the dynamics of neuronal assemblies. Previous work used a mean-field reduction method to determine the collective dynamics of a large heterogeneous network of uniformly and globally coupled theta neurons, which are a canonical formul...

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Main Authors: Lucas Lin, Ernest Barreto, Paul So
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-05-01
Series:Frontiers in Computational Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fncom.2020.00044/full
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spelling doaj-dcff877dce944426bde5f56f58c7c5182020-11-25T02:54:02ZengFrontiers Media S.A.Frontiers in Computational Neuroscience1662-51882020-05-011410.3389/fncom.2020.00044520545Synaptic Diversity Suppresses Complex Collective Behavior in Networks of Theta NeuronsLucas Lin0Ernest Barreto1Paul So2Department of Computer Science, Stanford University, Stanford, CA, United StatesDepartment of Physics and Astronomy and Interdisciplinary Program in Neuroscience, George Mason University, Fairfax, VA, United StatesDepartment of Physics and Astronomy and Interdisciplinary Program in Neuroscience, George Mason University, Fairfax, VA, United StatesComprehending how the brain functions requires an understanding of the dynamics of neuronal assemblies. Previous work used a mean-field reduction method to determine the collective dynamics of a large heterogeneous network of uniformly and globally coupled theta neurons, which are a canonical formulation of Type I neurons. However, in modeling neuronal networks, it is unreasonable to assume that the coupling strength between every pair of neurons is identical. The goal in the present work is to analytically examine the collective macroscopic behavior of a network of theta neurons that is more realistic in that it includes heterogeneity in the coupling strength as well as in neuronal excitability. We consider the occurrence of dynamical structures that give rise to complicated dynamics via bifurcations of macroscopic collective quantities, concentrating on two biophysically relevant cases: (1) predominantly excitable neurons with mostly excitatory connections, and (2) predominantly spiking neurons with inhibitory connections. We find that increasing the synaptic diversity moves these dynamical structures to distant extremes of parameter space, leaving simple collective equilibrium states in the physiologically relevant region. We also study the node vs. focus nature of stable macroscopic equilibrium solutions and discuss our results in the context of recent literature.https://www.frontiersin.org/article/10.3389/fncom.2020.00044/fullnetworksynaptic diversitytheta neuronoscillationssynchronizationheterogeneity
collection DOAJ
language English
format Article
sources DOAJ
author Lucas Lin
Ernest Barreto
Paul So
spellingShingle Lucas Lin
Ernest Barreto
Paul So
Synaptic Diversity Suppresses Complex Collective Behavior in Networks of Theta Neurons
Frontiers in Computational Neuroscience
network
synaptic diversity
theta neuron
oscillations
synchronization
heterogeneity
author_facet Lucas Lin
Ernest Barreto
Paul So
author_sort Lucas Lin
title Synaptic Diversity Suppresses Complex Collective Behavior in Networks of Theta Neurons
title_short Synaptic Diversity Suppresses Complex Collective Behavior in Networks of Theta Neurons
title_full Synaptic Diversity Suppresses Complex Collective Behavior in Networks of Theta Neurons
title_fullStr Synaptic Diversity Suppresses Complex Collective Behavior in Networks of Theta Neurons
title_full_unstemmed Synaptic Diversity Suppresses Complex Collective Behavior in Networks of Theta Neurons
title_sort synaptic diversity suppresses complex collective behavior in networks of theta neurons
publisher Frontiers Media S.A.
series Frontiers in Computational Neuroscience
issn 1662-5188
publishDate 2020-05-01
description Comprehending how the brain functions requires an understanding of the dynamics of neuronal assemblies. Previous work used a mean-field reduction method to determine the collective dynamics of a large heterogeneous network of uniformly and globally coupled theta neurons, which are a canonical formulation of Type I neurons. However, in modeling neuronal networks, it is unreasonable to assume that the coupling strength between every pair of neurons is identical. The goal in the present work is to analytically examine the collective macroscopic behavior of a network of theta neurons that is more realistic in that it includes heterogeneity in the coupling strength as well as in neuronal excitability. We consider the occurrence of dynamical structures that give rise to complicated dynamics via bifurcations of macroscopic collective quantities, concentrating on two biophysically relevant cases: (1) predominantly excitable neurons with mostly excitatory connections, and (2) predominantly spiking neurons with inhibitory connections. We find that increasing the synaptic diversity moves these dynamical structures to distant extremes of parameter space, leaving simple collective equilibrium states in the physiologically relevant region. We also study the node vs. focus nature of stable macroscopic equilibrium solutions and discuss our results in the context of recent literature.
topic network
synaptic diversity
theta neuron
oscillations
synchronization
heterogeneity
url https://www.frontiersin.org/article/10.3389/fncom.2020.00044/full
work_keys_str_mv AT lucaslin synapticdiversitysuppressescomplexcollectivebehaviorinnetworksofthetaneurons
AT ernestbarreto synapticdiversitysuppressescomplexcollectivebehaviorinnetworksofthetaneurons
AT paulso synapticdiversitysuppressescomplexcollectivebehaviorinnetworksofthetaneurons
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