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Spatially extended balanced networks without translationally invariant connectivity
Networks of neurons in the cerebral cortex exhibit a balance between excitation (positive input current) and inhibition (negative input current). Balanced network theory provides a parsimonious mathematical model of this excitatory-inhibitory balance using randomly connected networks of model neuron...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221049/ https://www.ncbi.nlm.nih.gov/pubmed/32405723 http://dx.doi.org/10.1186/s13408-020-00085-w |
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author | Ebsch, Christopher Rosenbaum, Robert |
author_facet | Ebsch, Christopher Rosenbaum, Robert |
author_sort | Ebsch, Christopher |
collection | PubMed |
description | Networks of neurons in the cerebral cortex exhibit a balance between excitation (positive input current) and inhibition (negative input current). Balanced network theory provides a parsimonious mathematical model of this excitatory-inhibitory balance using randomly connected networks of model neurons in which balance is realized as a stable fixed point of network dynamics in the limit of large network size. Balanced network theory reproduces many salient features of cortical network dynamics such as asynchronous-irregular spiking activity. Early studies of balanced networks did not account for the spatial topology of cortical networks. Later works introduced spatial connectivity structure, but were restricted to networks with translationally invariant connectivity structure in which connection probability depends on distance alone and boundaries are assumed to be periodic. Spatial connectivity structure in cortical network does not always satisfy these assumptions. We use the mathematical theory of integral equations to extend the mean-field theory of balanced networks to account for more general dependence of connection probability on the spatial location of pre- and postsynaptic neurons. We compare our mathematical derivations to simulations of large networks of recurrently connected spiking neuron models. |
format | Online Article Text |
id | pubmed-7221049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-72210492020-05-15 Spatially extended balanced networks without translationally invariant connectivity Ebsch, Christopher Rosenbaum, Robert J Math Neurosci Research Networks of neurons in the cerebral cortex exhibit a balance between excitation (positive input current) and inhibition (negative input current). Balanced network theory provides a parsimonious mathematical model of this excitatory-inhibitory balance using randomly connected networks of model neurons in which balance is realized as a stable fixed point of network dynamics in the limit of large network size. Balanced network theory reproduces many salient features of cortical network dynamics such as asynchronous-irregular spiking activity. Early studies of balanced networks did not account for the spatial topology of cortical networks. Later works introduced spatial connectivity structure, but were restricted to networks with translationally invariant connectivity structure in which connection probability depends on distance alone and boundaries are assumed to be periodic. Spatial connectivity structure in cortical network does not always satisfy these assumptions. We use the mathematical theory of integral equations to extend the mean-field theory of balanced networks to account for more general dependence of connection probability on the spatial location of pre- and postsynaptic neurons. We compare our mathematical derivations to simulations of large networks of recurrently connected spiking neuron models. Springer Berlin Heidelberg 2020-05-13 /pmc/articles/PMC7221049/ /pubmed/32405723 http://dx.doi.org/10.1186/s13408-020-00085-w 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Ebsch, Christopher Rosenbaum, Robert Spatially extended balanced networks without translationally invariant connectivity |
title | Spatially extended balanced networks without translationally invariant connectivity |
title_full | Spatially extended balanced networks without translationally invariant connectivity |
title_fullStr | Spatially extended balanced networks without translationally invariant connectivity |
title_full_unstemmed | Spatially extended balanced networks without translationally invariant connectivity |
title_short | Spatially extended balanced networks without translationally invariant connectivity |
title_sort | spatially extended balanced networks without translationally invariant connectivity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221049/ https://www.ncbi.nlm.nih.gov/pubmed/32405723 http://dx.doi.org/10.1186/s13408-020-00085-w |
work_keys_str_mv | AT ebschchristopher spatiallyextendedbalancednetworkswithouttranslationallyinvariantconnectivity AT rosenbaumrobert spatiallyextendedbalancednetworkswithouttranslationallyinvariantconnectivity |