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Criticality predicts maximum irregularity in recurrent networks of excitatory nodes
A rigorous understanding of brain dynamics and function requires a conceptual bridge between multiple levels of organization, including neural spiking and network-level population activity. Mounting evidence suggests that neural networks of cerebral cortex operate at a critical regime, which is defi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560579/ https://www.ncbi.nlm.nih.gov/pubmed/28817580 http://dx.doi.org/10.1371/journal.pone.0182501 |
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author | Karimipanah, Yahya Ma, Zhengyu Wessel, Ralf |
author_facet | Karimipanah, Yahya Ma, Zhengyu Wessel, Ralf |
author_sort | Karimipanah, Yahya |
collection | PubMed |
description | A rigorous understanding of brain dynamics and function requires a conceptual bridge between multiple levels of organization, including neural spiking and network-level population activity. Mounting evidence suggests that neural networks of cerebral cortex operate at a critical regime, which is defined as a transition point between two phases of short lasting and chaotic activity. However, despite the fact that criticality brings about certain functional advantages for information processing, its supporting evidence is still far from conclusive, as it has been mostly based on power law scaling of size and durations of cascades of activity. Moreover, to what degree such hypothesis could explain some fundamental features of neural activity is still largely unknown. One of the most prevalent features of cortical activity in vivo is known to be spike irregularity of spike trains, which is measured in terms of the coefficient of variation (CV) larger than one. Here, using a minimal computational model of excitatory nodes, we show that irregular spiking (CV > 1) naturally emerges in a recurrent network operating at criticality. More importantly, we show that even at the presence of other sources of spike irregularity, being at criticality maximizes the mean coefficient of variation of neurons, thereby maximizing their spike irregularity. Furthermore, we also show that such a maximized irregularity results in maximum correlation between neuronal firing rates and their corresponding spike irregularity (measured in terms of CV). On the one hand, using a model in the universality class of directed percolation, we propose new hallmarks of criticality at single-unit level, which could be applicable to any network of excitable nodes. On the other hand, given the controversy of the neural criticality hypothesis, we discuss the limitation of this approach to neural systems and to what degree they support the criticality hypothesis in real neural networks. Finally, we discuss the limitations of applying our results to real networks and to what degree they support the criticality hypothesis. |
format | Online Article Text |
id | pubmed-5560579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55605792017-08-25 Criticality predicts maximum irregularity in recurrent networks of excitatory nodes Karimipanah, Yahya Ma, Zhengyu Wessel, Ralf PLoS One Research Article A rigorous understanding of brain dynamics and function requires a conceptual bridge between multiple levels of organization, including neural spiking and network-level population activity. Mounting evidence suggests that neural networks of cerebral cortex operate at a critical regime, which is defined as a transition point between two phases of short lasting and chaotic activity. However, despite the fact that criticality brings about certain functional advantages for information processing, its supporting evidence is still far from conclusive, as it has been mostly based on power law scaling of size and durations of cascades of activity. Moreover, to what degree such hypothesis could explain some fundamental features of neural activity is still largely unknown. One of the most prevalent features of cortical activity in vivo is known to be spike irregularity of spike trains, which is measured in terms of the coefficient of variation (CV) larger than one. Here, using a minimal computational model of excitatory nodes, we show that irregular spiking (CV > 1) naturally emerges in a recurrent network operating at criticality. More importantly, we show that even at the presence of other sources of spike irregularity, being at criticality maximizes the mean coefficient of variation of neurons, thereby maximizing their spike irregularity. Furthermore, we also show that such a maximized irregularity results in maximum correlation between neuronal firing rates and their corresponding spike irregularity (measured in terms of CV). On the one hand, using a model in the universality class of directed percolation, we propose new hallmarks of criticality at single-unit level, which could be applicable to any network of excitable nodes. On the other hand, given the controversy of the neural criticality hypothesis, we discuss the limitation of this approach to neural systems and to what degree they support the criticality hypothesis in real neural networks. Finally, we discuss the limitations of applying our results to real networks and to what degree they support the criticality hypothesis. Public Library of Science 2017-08-17 /pmc/articles/PMC5560579/ /pubmed/28817580 http://dx.doi.org/10.1371/journal.pone.0182501 Text en © 2017 Karimipanah et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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 Karimipanah, Yahya Ma, Zhengyu Wessel, Ralf Criticality predicts maximum irregularity in recurrent networks of excitatory nodes |
title | Criticality predicts maximum irregularity in recurrent networks of excitatory nodes |
title_full | Criticality predicts maximum irregularity in recurrent networks of excitatory nodes |
title_fullStr | Criticality predicts maximum irregularity in recurrent networks of excitatory nodes |
title_full_unstemmed | Criticality predicts maximum irregularity in recurrent networks of excitatory nodes |
title_short | Criticality predicts maximum irregularity in recurrent networks of excitatory nodes |
title_sort | criticality predicts maximum irregularity in recurrent networks of excitatory nodes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560579/ https://www.ncbi.nlm.nih.gov/pubmed/28817580 http://dx.doi.org/10.1371/journal.pone.0182501 |
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