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Unsupervised Learning of Persistent and Sequential Activity
Two strikingly distinct types of activity have been observed in various brain structures during delay periods of delayed response tasks: Persistent activity (PA), in which a sub-population of neurons maintains an elevated firing rate throughout an entire delay period; and Sequential activity (SA), i...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978734/ https://www.ncbi.nlm.nih.gov/pubmed/32009924 http://dx.doi.org/10.3389/fncom.2019.00097 |
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author | Pereira, Ulises Brunel, Nicolas |
author_facet | Pereira, Ulises Brunel, Nicolas |
author_sort | Pereira, Ulises |
collection | PubMed |
description | Two strikingly distinct types of activity have been observed in various brain structures during delay periods of delayed response tasks: Persistent activity (PA), in which a sub-population of neurons maintains an elevated firing rate throughout an entire delay period; and Sequential activity (SA), in which sub-populations of neurons are activated sequentially in time. It has been hypothesized that both types of dynamics can be “learned” by the relevant networks from the statistics of their inputs, thanks to mechanisms of synaptic plasticity. However, the necessary conditions for a synaptic plasticity rule and input statistics to learn these two types of dynamics in a stable fashion are still unclear. In particular, it is unclear whether a single learning rule is able to learn both types of activity patterns, depending on the statistics of the inputs driving the network. Here, we first characterize the complete bifurcation diagram of a firing rate model of multiple excitatory populations with an inhibitory mechanism, as a function of the parameters characterizing its connectivity. We then investigate how an unsupervised temporally asymmetric Hebbian plasticity rule shapes the dynamics of the network. Consistent with previous studies, we find that for stable learning of PA and SA, an additional stabilization mechanism is necessary. We show that a generalized version of the standard multiplicative homeostatic plasticity (Renart et al., 2003; Toyoizumi et al., 2014) stabilizes learning by effectively masking excitatory connections during stimulation and unmasking those connections during retrieval. Using the bifurcation diagram derived for fixed connectivity, we study analytically the temporal evolution and the steady state of the learned recurrent architecture as a function of parameters characterizing the external inputs. Slow changing stimuli lead to PA, while fast changing stimuli lead to SA. Our network model shows how a network with plastic synapses can stably and flexibly learn PA and SA in an unsupervised manner. |
format | Online Article Text |
id | pubmed-6978734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69787342020-02-01 Unsupervised Learning of Persistent and Sequential Activity Pereira, Ulises Brunel, Nicolas Front Comput Neurosci Neuroscience Two strikingly distinct types of activity have been observed in various brain structures during delay periods of delayed response tasks: Persistent activity (PA), in which a sub-population of neurons maintains an elevated firing rate throughout an entire delay period; and Sequential activity (SA), in which sub-populations of neurons are activated sequentially in time. It has been hypothesized that both types of dynamics can be “learned” by the relevant networks from the statistics of their inputs, thanks to mechanisms of synaptic plasticity. However, the necessary conditions for a synaptic plasticity rule and input statistics to learn these two types of dynamics in a stable fashion are still unclear. In particular, it is unclear whether a single learning rule is able to learn both types of activity patterns, depending on the statistics of the inputs driving the network. Here, we first characterize the complete bifurcation diagram of a firing rate model of multiple excitatory populations with an inhibitory mechanism, as a function of the parameters characterizing its connectivity. We then investigate how an unsupervised temporally asymmetric Hebbian plasticity rule shapes the dynamics of the network. Consistent with previous studies, we find that for stable learning of PA and SA, an additional stabilization mechanism is necessary. We show that a generalized version of the standard multiplicative homeostatic plasticity (Renart et al., 2003; Toyoizumi et al., 2014) stabilizes learning by effectively masking excitatory connections during stimulation and unmasking those connections during retrieval. Using the bifurcation diagram derived for fixed connectivity, we study analytically the temporal evolution and the steady state of the learned recurrent architecture as a function of parameters characterizing the external inputs. Slow changing stimuli lead to PA, while fast changing stimuli lead to SA. Our network model shows how a network with plastic synapses can stably and flexibly learn PA and SA in an unsupervised manner. Frontiers Media S.A. 2020-01-17 /pmc/articles/PMC6978734/ /pubmed/32009924 http://dx.doi.org/10.3389/fncom.2019.00097 Text en Copyright © 2020 Pereira and Brunel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Pereira, Ulises Brunel, Nicolas Unsupervised Learning of Persistent and Sequential Activity |
title | Unsupervised Learning of Persistent and Sequential Activity |
title_full | Unsupervised Learning of Persistent and Sequential Activity |
title_fullStr | Unsupervised Learning of Persistent and Sequential Activity |
title_full_unstemmed | Unsupervised Learning of Persistent and Sequential Activity |
title_short | Unsupervised Learning of Persistent and Sequential Activity |
title_sort | unsupervised learning of persistent and sequential activity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978734/ https://www.ncbi.nlm.nih.gov/pubmed/32009924 http://dx.doi.org/10.3389/fncom.2019.00097 |
work_keys_str_mv | AT pereiraulises unsupervisedlearningofpersistentandsequentialactivity AT brunelnicolas unsupervisedlearningofpersistentandsequentialactivity |