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Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activity
Spike-timing-dependent plasticity (STDP) has been well established between excitatory neurons and several computational functions have been proposed in various neural systems. Despite some recent efforts, however, there is a significant lack of functional understanding of inhibitory STDP (iSTDP) and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019846/ https://www.ncbi.nlm.nih.gov/pubmed/24847242 http://dx.doi.org/10.3389/fncom.2014.00053 |
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author | Kleberg, Florence I. Fukai, Tomoki Gilson, Matthieu |
author_facet | Kleberg, Florence I. Fukai, Tomoki Gilson, Matthieu |
author_sort | Kleberg, Florence I. |
collection | PubMed |
description | Spike-timing-dependent plasticity (STDP) has been well established between excitatory neurons and several computational functions have been proposed in various neural systems. Despite some recent efforts, however, there is a significant lack of functional understanding of inhibitory STDP (iSTDP) and its interplay with excitatory STDP (eSTDP). Here, we demonstrate by analytical and numerical methods that iSTDP contributes crucially to the balance of excitatory and inhibitory weights for the selection of a specific signaling pathway among other pathways in a feedforward circuit. This pathway selection is based on the high sensitivity of STDP to correlations in spike times, which complements a recent proposal for the role of iSTDP in firing-rate based selection. Our model predicts that asymmetric anti-Hebbian iSTDP exceeds asymmetric Hebbian iSTDP for supporting pathway-specific balance, which we show is useful for propagating transient neuronal responses. Furthermore, we demonstrate how STDPs at excitatory–excitatory, excitatory–inhibitory, and inhibitory–excitatory synapses cooperate to improve the pathway selection. We propose that iSTDP is crucial for shaping the network structure that achieves efficient processing of synchronous spikes. |
format | Online Article Text |
id | pubmed-4019846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40198462014-05-20 Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activity Kleberg, Florence I. Fukai, Tomoki Gilson, Matthieu Front Comput Neurosci Neuroscience Spike-timing-dependent plasticity (STDP) has been well established between excitatory neurons and several computational functions have been proposed in various neural systems. Despite some recent efforts, however, there is a significant lack of functional understanding of inhibitory STDP (iSTDP) and its interplay with excitatory STDP (eSTDP). Here, we demonstrate by analytical and numerical methods that iSTDP contributes crucially to the balance of excitatory and inhibitory weights for the selection of a specific signaling pathway among other pathways in a feedforward circuit. This pathway selection is based on the high sensitivity of STDP to correlations in spike times, which complements a recent proposal for the role of iSTDP in firing-rate based selection. Our model predicts that asymmetric anti-Hebbian iSTDP exceeds asymmetric Hebbian iSTDP for supporting pathway-specific balance, which we show is useful for propagating transient neuronal responses. Furthermore, we demonstrate how STDPs at excitatory–excitatory, excitatory–inhibitory, and inhibitory–excitatory synapses cooperate to improve the pathway selection. We propose that iSTDP is crucial for shaping the network structure that achieves efficient processing of synchronous spikes. Frontiers Media S.A. 2014-05-07 /pmc/articles/PMC4019846/ /pubmed/24847242 http://dx.doi.org/10.3389/fncom.2014.00053 Text en Copyright © 2014 Kleberg, Fukai and Gilson. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Kleberg, Florence I. Fukai, Tomoki Gilson, Matthieu Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activity |
title | Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activity |
title_full | Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activity |
title_fullStr | Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activity |
title_full_unstemmed | Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activity |
title_short | Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activity |
title_sort | excitatory and inhibitory stdp jointly tune feedforward neural circuits to selectively propagate correlated spiking activity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019846/ https://www.ncbi.nlm.nih.gov/pubmed/24847242 http://dx.doi.org/10.3389/fncom.2014.00053 |
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