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Emergence of global synchronization in directed excitatory networks of type I neurons
The collective behaviour of neural networks depends on the cellular and synaptic properties of the neurons. The phase-response curve (PRC) is an experimentally obtainable measure of cellular properties that quantifies the shift in the next spike time of a neuron as a function of the phase at which s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039997/ https://www.ncbi.nlm.nih.gov/pubmed/32094415 http://dx.doi.org/10.1038/s41598-020-60205-0 |
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author | Ziaeemehr, Abolfazl Zarei, Mina Sheshbolouki, Aida |
author_facet | Ziaeemehr, Abolfazl Zarei, Mina Sheshbolouki, Aida |
author_sort | Ziaeemehr, Abolfazl |
collection | PubMed |
description | The collective behaviour of neural networks depends on the cellular and synaptic properties of the neurons. The phase-response curve (PRC) is an experimentally obtainable measure of cellular properties that quantifies the shift in the next spike time of a neuron as a function of the phase at which stimulus is delivered to that neuron. The neuronal PRCs can be classified as having either purely positive values (type I) or distinct positive and negative regions (type II). Networks of type 1 PRCs tend not to synchronize via mutual excitatory synaptic connections. We study the synchronization properties of identical type I and type II neurons, assuming unidirectional synapses. Performing the linear stability analysis and the numerical simulation of the extended Kuramoto model, we show that feedforward loop motifs favour synchronization of type I excitatory and inhibitory neurons, while feedback loop motifs destroy their synchronization tendency. Moreover, large directed networks, either without feedback motifs or with many of them, have been constructed from the same undirected backbones, and a high synchronization level is observed for directed acyclic graphs with type I neurons. It has been shown that, the synchronizability of type I neurons depends on both the directionality of the network connectivity and the topology of its undirected backbone. The abundance of feedforward motifs enhances the synchronizability of the directed acyclic graphs. |
format | Online Article Text |
id | pubmed-7039997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70399972020-03-03 Emergence of global synchronization in directed excitatory networks of type I neurons Ziaeemehr, Abolfazl Zarei, Mina Sheshbolouki, Aida Sci Rep Article The collective behaviour of neural networks depends on the cellular and synaptic properties of the neurons. The phase-response curve (PRC) is an experimentally obtainable measure of cellular properties that quantifies the shift in the next spike time of a neuron as a function of the phase at which stimulus is delivered to that neuron. The neuronal PRCs can be classified as having either purely positive values (type I) or distinct positive and negative regions (type II). Networks of type 1 PRCs tend not to synchronize via mutual excitatory synaptic connections. We study the synchronization properties of identical type I and type II neurons, assuming unidirectional synapses. Performing the linear stability analysis and the numerical simulation of the extended Kuramoto model, we show that feedforward loop motifs favour synchronization of type I excitatory and inhibitory neurons, while feedback loop motifs destroy their synchronization tendency. Moreover, large directed networks, either without feedback motifs or with many of them, have been constructed from the same undirected backbones, and a high synchronization level is observed for directed acyclic graphs with type I neurons. It has been shown that, the synchronizability of type I neurons depends on both the directionality of the network connectivity and the topology of its undirected backbone. The abundance of feedforward motifs enhances the synchronizability of the directed acyclic graphs. Nature Publishing Group UK 2020-02-24 /pmc/articles/PMC7039997/ /pubmed/32094415 http://dx.doi.org/10.1038/s41598-020-60205-0 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ziaeemehr, Abolfazl Zarei, Mina Sheshbolouki, Aida Emergence of global synchronization in directed excitatory networks of type I neurons |
title | Emergence of global synchronization in directed excitatory networks of type I neurons |
title_full | Emergence of global synchronization in directed excitatory networks of type I neurons |
title_fullStr | Emergence of global synchronization in directed excitatory networks of type I neurons |
title_full_unstemmed | Emergence of global synchronization in directed excitatory networks of type I neurons |
title_short | Emergence of global synchronization in directed excitatory networks of type I neurons |
title_sort | emergence of global synchronization in directed excitatory networks of type i neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039997/ https://www.ncbi.nlm.nih.gov/pubmed/32094415 http://dx.doi.org/10.1038/s41598-020-60205-0 |
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