Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1782183274186014720 |
---|---|
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. |
format | Text |
id | pubmed-2895637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT bushdaniel dualcodingwithstdpinaspikingrecurrentneuralnetworkmodelofthehippocampus AT philippidesandrew dualcodingwithstdpinaspikingrecurrentneuralnetworkmodelofthehippocampus AT husbandsphil dualcodingwithstdpinaspikingrecurrentneuralnetworkmodelofthehippocampus AT osheamichael dualcodingwithstdpinaspikingrecurrentneuralnetworkmodelofthehippocampus |