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Dual Coding with STDP in a Spiking Recurrent Neural Network Model of the Hippocampus

The firing rate of single neurons in the mammalian hippocampus has been demonstrated to encode for a range of spatial and non-spatial stimuli. It has also been demonstrated that phase of firing, with respect to the theta oscillation that dominates the hippocampal EEG during stereotype learning behav...

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Detalles Bibliográficos
Autores principales: Bush, Daniel, Philippides, Andrew, Husbands, Phil, O'Shea, Michael
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895637/
https://www.ncbi.nlm.nih.gov/pubmed/20617201
http://dx.doi.org/10.1371/journal.pcbi.1000839
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author Bush, Daniel
Philippides, Andrew
Husbands, Phil
O'Shea, Michael
author_facet Bush, Daniel
Philippides, Andrew
Husbands, Phil
O'Shea, Michael
author_sort Bush, Daniel
collection PubMed
description The firing rate of single neurons in the mammalian hippocampus has been demonstrated to encode for a range of spatial and non-spatial stimuli. It has also been demonstrated that phase of firing, with respect to the theta oscillation that dominates the hippocampal EEG during stereotype learning behaviour, correlates with an animal's spatial location. These findings have led to the hypothesis that the hippocampus operates using a dual (rate and temporal) coding system. To investigate the phenomenon of dual coding in the hippocampus, we examine a spiking recurrent network model with theta coded neural dynamics and an STDP rule that mediates rate-coded Hebbian learning when pre- and post-synaptic firing is stochastic. We demonstrate that this plasticity rule can generate both symmetric and asymmetric connections between neurons that fire at concurrent or successive theta phase, respectively, and subsequently produce both pattern completion and sequence prediction from partial cues. This unifies previously disparate auto- and hetero-associative network models of hippocampal function and provides them with a firmer basis in modern neurobiology. Furthermore, the encoding and reactivation of activity in mutually exciting Hebbian cell assemblies demonstrated here is believed to represent a fundamental mechanism of cognitive processing in the brain.
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spelling pubmed-28956372010-07-08 Dual Coding with STDP in a Spiking Recurrent Neural Network Model of the Hippocampus Bush, Daniel Philippides, Andrew Husbands, Phil O'Shea, Michael PLoS Comput Biol Research Article The firing rate of single neurons in the mammalian hippocampus has been demonstrated to encode for a range of spatial and non-spatial stimuli. It has also been demonstrated that phase of firing, with respect to the theta oscillation that dominates the hippocampal EEG during stereotype learning behaviour, correlates with an animal's spatial location. These findings have led to the hypothesis that the hippocampus operates using a dual (rate and temporal) coding system. To investigate the phenomenon of dual coding in the hippocampus, we examine a spiking recurrent network model with theta coded neural dynamics and an STDP rule that mediates rate-coded Hebbian learning when pre- and post-synaptic firing is stochastic. We demonstrate that this plasticity rule can generate both symmetric and asymmetric connections between neurons that fire at concurrent or successive theta phase, respectively, and subsequently produce both pattern completion and sequence prediction from partial cues. This unifies previously disparate auto- and hetero-associative network models of hippocampal function and provides them with a firmer basis in modern neurobiology. Furthermore, the encoding and reactivation of activity in mutually exciting Hebbian cell assemblies demonstrated here is believed to represent a fundamental mechanism of cognitive processing in the brain. Public Library of Science 2010-07-01 /pmc/articles/PMC2895637/ /pubmed/20617201 http://dx.doi.org/10.1371/journal.pcbi.1000839 Text en Bush 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bush, Daniel
Philippides, Andrew
Husbands, Phil
O'Shea, Michael
Dual Coding with STDP in a Spiking Recurrent Neural Network Model of the Hippocampus
title Dual Coding with STDP in a Spiking Recurrent Neural Network Model of the Hippocampus
title_full Dual Coding with STDP in a Spiking Recurrent Neural Network Model of the Hippocampus
title_fullStr Dual Coding with STDP in a Spiking Recurrent Neural Network Model of the Hippocampus
title_full_unstemmed Dual Coding with STDP in a Spiking Recurrent Neural Network Model of the Hippocampus
title_short Dual Coding with STDP in a Spiking Recurrent Neural Network Model of the Hippocampus
title_sort dual coding with stdp in a spiking recurrent neural network model of the hippocampus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895637/
https://www.ncbi.nlm.nih.gov/pubmed/20617201
http://dx.doi.org/10.1371/journal.pcbi.1000839
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