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E-I balance emerges naturally from continuous Hebbian learning in autonomous neural networks
Spontaneous brain activity is characterized in part by a balanced asynchronous chaotic state. Cortical recordings show that excitatory (E) and inhibitory (I) drivings in the E-I balanced state are substantially larger than the overall input. We show that such a state arises naturally in fully adapti...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5997746/ https://www.ncbi.nlm.nih.gov/pubmed/29895972 http://dx.doi.org/10.1038/s41598-018-27099-5 |
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author | Trapp, Philip Echeveste, Rodrigo Gros, Claudius |
author_facet | Trapp, Philip Echeveste, Rodrigo Gros, Claudius |
author_sort | Trapp, Philip |
collection | PubMed |
description | Spontaneous brain activity is characterized in part by a balanced asynchronous chaotic state. Cortical recordings show that excitatory (E) and inhibitory (I) drivings in the E-I balanced state are substantially larger than the overall input. We show that such a state arises naturally in fully adapting networks which are deterministic, autonomously active and not subject to stochastic external or internal drivings. Temporary imbalances between excitatory and inhibitory inputs lead to large but short-lived activity bursts that stabilize irregular dynamics. We simulate autonomous networks of rate-encoding neurons for which all synaptic weights are plastic and subject to a Hebbian plasticity rule, the flux rule, that can be derived from the stationarity principle of statistical learning. Moreover, the average firing rate is regulated individually via a standard homeostatic adaption of the bias of each neuron’s input-output non-linear function. Additionally, networks with and without short-term plasticity are considered. E-I balance may arise only when the mean excitatory and inhibitory weights are themselves balanced, modulo the overall activity level. We show that synaptic weight balance, which has been considered hitherto as given, naturally arises in autonomous neural networks when the here considered self-limiting Hebbian synaptic plasticity rule is continuously active. |
format | Online Article Text |
id | pubmed-5997746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59977462018-06-21 E-I balance emerges naturally from continuous Hebbian learning in autonomous neural networks Trapp, Philip Echeveste, Rodrigo Gros, Claudius Sci Rep Article Spontaneous brain activity is characterized in part by a balanced asynchronous chaotic state. Cortical recordings show that excitatory (E) and inhibitory (I) drivings in the E-I balanced state are substantially larger than the overall input. We show that such a state arises naturally in fully adapting networks which are deterministic, autonomously active and not subject to stochastic external or internal drivings. Temporary imbalances between excitatory and inhibitory inputs lead to large but short-lived activity bursts that stabilize irregular dynamics. We simulate autonomous networks of rate-encoding neurons for which all synaptic weights are plastic and subject to a Hebbian plasticity rule, the flux rule, that can be derived from the stationarity principle of statistical learning. Moreover, the average firing rate is regulated individually via a standard homeostatic adaption of the bias of each neuron’s input-output non-linear function. Additionally, networks with and without short-term plasticity are considered. E-I balance may arise only when the mean excitatory and inhibitory weights are themselves balanced, modulo the overall activity level. We show that synaptic weight balance, which has been considered hitherto as given, naturally arises in autonomous neural networks when the here considered self-limiting Hebbian synaptic plasticity rule is continuously active. Nature Publishing Group UK 2018-06-12 /pmc/articles/PMC5997746/ /pubmed/29895972 http://dx.doi.org/10.1038/s41598-018-27099-5 Text en © The Author(s) 2018 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 Trapp, Philip Echeveste, Rodrigo Gros, Claudius E-I balance emerges naturally from continuous Hebbian learning in autonomous neural networks |
title | E-I balance emerges naturally from continuous Hebbian learning in autonomous neural networks |
title_full | E-I balance emerges naturally from continuous Hebbian learning in autonomous neural networks |
title_fullStr | E-I balance emerges naturally from continuous Hebbian learning in autonomous neural networks |
title_full_unstemmed | E-I balance emerges naturally from continuous Hebbian learning in autonomous neural networks |
title_short | E-I balance emerges naturally from continuous Hebbian learning in autonomous neural networks |
title_sort | e-i balance emerges naturally from continuous hebbian learning in autonomous neural networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5997746/ https://www.ncbi.nlm.nih.gov/pubmed/29895972 http://dx.doi.org/10.1038/s41598-018-27099-5 |
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