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Asynchronous Rate Chaos in Spiking Neuronal Circuits
The brain exhibits temporally complex patterns of activity with features similar to those of chaotic systems. Theoretical studies over the last twenty years have described various computational advantages for such regimes in neuronal systems. Nevertheless, it still remains unclear whether chaos requ...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521798/ https://www.ncbi.nlm.nih.gov/pubmed/26230679 http://dx.doi.org/10.1371/journal.pcbi.1004266 |
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author | Harish, Omri Hansel, David |
author_facet | Harish, Omri Hansel, David |
author_sort | Harish, Omri |
collection | PubMed |
description | The brain exhibits temporally complex patterns of activity with features similar to those of chaotic systems. Theoretical studies over the last twenty years have described various computational advantages for such regimes in neuronal systems. Nevertheless, it still remains unclear whether chaos requires specific cellular properties or network architectures, or whether it is a generic property of neuronal circuits. We investigate the dynamics of networks of excitatory-inhibitory (EI) spiking neurons with random sparse connectivity operating in the regime of balance of excitation and inhibition. Combining Dynamical Mean-Field Theory with numerical simulations, we show that chaotic, asynchronous firing rate fluctuations emerge generically for sufficiently strong synapses. Two different mechanisms can lead to these chaotic fluctuations. One mechanism relies on slow I-I inhibition which gives rise to slow subthreshold voltage and rate fluctuations. The decorrelation time of these fluctuations is proportional to the time constant of the inhibition. The second mechanism relies on the recurrent E-I-E feedback loop. It requires slow excitation but the inhibition can be fast. In the corresponding dynamical regime all neurons exhibit rate fluctuations on the time scale of the excitation. Another feature of this regime is that the population-averaged firing rate is substantially smaller in the excitatory population than in the inhibitory population. This is not necessarily the case in the I-I mechanism. Finally, we discuss the neurophysiological and computational significance of our results. |
format | Online Article Text |
id | pubmed-4521798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45217982015-08-06 Asynchronous Rate Chaos in Spiking Neuronal Circuits Harish, Omri Hansel, David PLoS Comput Biol Research Article The brain exhibits temporally complex patterns of activity with features similar to those of chaotic systems. Theoretical studies over the last twenty years have described various computational advantages for such regimes in neuronal systems. Nevertheless, it still remains unclear whether chaos requires specific cellular properties or network architectures, or whether it is a generic property of neuronal circuits. We investigate the dynamics of networks of excitatory-inhibitory (EI) spiking neurons with random sparse connectivity operating in the regime of balance of excitation and inhibition. Combining Dynamical Mean-Field Theory with numerical simulations, we show that chaotic, asynchronous firing rate fluctuations emerge generically for sufficiently strong synapses. Two different mechanisms can lead to these chaotic fluctuations. One mechanism relies on slow I-I inhibition which gives rise to slow subthreshold voltage and rate fluctuations. The decorrelation time of these fluctuations is proportional to the time constant of the inhibition. The second mechanism relies on the recurrent E-I-E feedback loop. It requires slow excitation but the inhibition can be fast. In the corresponding dynamical regime all neurons exhibit rate fluctuations on the time scale of the excitation. Another feature of this regime is that the population-averaged firing rate is substantially smaller in the excitatory population than in the inhibitory population. This is not necessarily the case in the I-I mechanism. Finally, we discuss the neurophysiological and computational significance of our results. Public Library of Science 2015-07-31 /pmc/articles/PMC4521798/ /pubmed/26230679 http://dx.doi.org/10.1371/journal.pcbi.1004266 Text en © 2015 Harish, Hansel http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Harish, Omri Hansel, David Asynchronous Rate Chaos in Spiking Neuronal Circuits |
title | Asynchronous Rate Chaos in Spiking Neuronal Circuits |
title_full | Asynchronous Rate Chaos in Spiking Neuronal Circuits |
title_fullStr | Asynchronous Rate Chaos in Spiking Neuronal Circuits |
title_full_unstemmed | Asynchronous Rate Chaos in Spiking Neuronal Circuits |
title_short | Asynchronous Rate Chaos in Spiking Neuronal Circuits |
title_sort | asynchronous rate chaos in spiking neuronal circuits |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521798/ https://www.ncbi.nlm.nih.gov/pubmed/26230679 http://dx.doi.org/10.1371/journal.pcbi.1004266 |
work_keys_str_mv | AT harishomri asynchronousratechaosinspikingneuronalcircuits AT hanseldavid asynchronousratechaosinspikingneuronalcircuits |