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Introducing double bouquet cells into a modular cortical associative memory model

We present an electrophysiological model of double bouquet cells and integrate them into an established cortical columnar microcircuit model that has previously been used as a spiking attractor model for memory. Learning in that model relies on a Hebbian-Bayesian learning rule to condition recurrent...

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Detalles Bibliográficos
Autores principales: Chrysanthidis, Nikolaos, Fiebig, Florian, Lansner, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879442/
https://www.ncbi.nlm.nih.gov/pubmed/31502234
http://dx.doi.org/10.1007/s10827-019-00729-1
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author Chrysanthidis, Nikolaos
Fiebig, Florian
Lansner, Anders
author_facet Chrysanthidis, Nikolaos
Fiebig, Florian
Lansner, Anders
author_sort Chrysanthidis, Nikolaos
collection PubMed
description We present an electrophysiological model of double bouquet cells and integrate them into an established cortical columnar microcircuit model that has previously been used as a spiking attractor model for memory. Learning in that model relies on a Hebbian-Bayesian learning rule to condition recurrent connectivity between pyramidal cells. We here demonstrate that the inclusion of a biophysically plausible double bouquet cell model can solve earlier concerns about learning rules that simultaneously learn excitation and inhibition and might thus violate Dale’s principle. We show that learning ability and resulting effective connectivity between functional columns of previous network models is preserved when pyramidal synapses onto double bouquet cells are plastic under the same Hebbian-Bayesian learning rule. The proposed architecture draws on experimental evidence on double bouquet cells and effectively solves the problem of duplexed learning of inhibition and excitation by replacing recurrent inhibition between pyramidal cells in functional columns of different stimulus selectivity with a plastic disynaptic pathway. We thus show that the resulting change to the microcircuit architecture improves the model’s biological plausibility without otherwise impacting the model’s spiking activity, basic operation, and learning abilities.
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spelling pubmed-68794422019-12-10 Introducing double bouquet cells into a modular cortical associative memory model Chrysanthidis, Nikolaos Fiebig, Florian Lansner, Anders J Comput Neurosci Article We present an electrophysiological model of double bouquet cells and integrate them into an established cortical columnar microcircuit model that has previously been used as a spiking attractor model for memory. Learning in that model relies on a Hebbian-Bayesian learning rule to condition recurrent connectivity between pyramidal cells. We here demonstrate that the inclusion of a biophysically plausible double bouquet cell model can solve earlier concerns about learning rules that simultaneously learn excitation and inhibition and might thus violate Dale’s principle. We show that learning ability and resulting effective connectivity between functional columns of previous network models is preserved when pyramidal synapses onto double bouquet cells are plastic under the same Hebbian-Bayesian learning rule. The proposed architecture draws on experimental evidence on double bouquet cells and effectively solves the problem of duplexed learning of inhibition and excitation by replacing recurrent inhibition between pyramidal cells in functional columns of different stimulus selectivity with a plastic disynaptic pathway. We thus show that the resulting change to the microcircuit architecture improves the model’s biological plausibility without otherwise impacting the model’s spiking activity, basic operation, and learning abilities. Springer US 2019-09-09 2019 /pmc/articles/PMC6879442/ /pubmed/31502234 http://dx.doi.org/10.1007/s10827-019-00729-1 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Article
Chrysanthidis, Nikolaos
Fiebig, Florian
Lansner, Anders
Introducing double bouquet cells into a modular cortical associative memory model
title Introducing double bouquet cells into a modular cortical associative memory model
title_full Introducing double bouquet cells into a modular cortical associative memory model
title_fullStr Introducing double bouquet cells into a modular cortical associative memory model
title_full_unstemmed Introducing double bouquet cells into a modular cortical associative memory model
title_short Introducing double bouquet cells into a modular cortical associative memory model
title_sort introducing double bouquet cells into a modular cortical associative memory model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879442/
https://www.ncbi.nlm.nih.gov/pubmed/31502234
http://dx.doi.org/10.1007/s10827-019-00729-1
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