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...
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Format: | Article |
Language: | English |
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Frontiers Media S.A.
2014-05-01
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Series: | Frontiers in Computational Neuroscience |
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Online Access: | http://journal.frontiersin.org/Journal/10.3389/fncom.2014.00053/full |
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author | Florence I Kleberg Tomoki eFukai Matthieu eGilson |
author_facet | Florence I Kleberg Tomoki eFukai Matthieu eGilson |
author_sort | Florence I Kleberg |
collection | DOAJ |
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. |
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id | doaj.art-ba542f114ea04c39ab6e7208a8e42c8c |
institution | Directory Open Access Journal |
issn | 1662-5188 |
language | English |
last_indexed | 2024-12-21T23:09:27Z |
publishDate | 2014-05-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Computational Neuroscience |
spelling | doaj.art-ba542f114ea04c39ab6e7208a8e42c8c2022-12-21T18:47:04ZengFrontiers Media S.A.Frontiers in Computational Neuroscience1662-51882014-05-01810.3389/fncom.2014.0005375822Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activityFlorence I Kleberg0Tomoki eFukai1Matthieu eGilson2RIKEN Brain Science InstituteRIKEN Brain Science InstituteRIKEN Brain Science InstituteSpike-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.http://journal.frontiersin.org/Journal/10.3389/fncom.2014.00053/fullbalanceexcitationinhibitionSTDPCorrelationpropagation |
spellingShingle | Florence I Kleberg Tomoki eFukai Matthieu eGilson Excitatory and inhibitory STDP jointly tune feedforward neural circuits to selectively propagate correlated spiking activity Frontiers in Computational Neuroscience balance excitation inhibition STDP Correlation propagation |
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 | balance excitation inhibition STDP Correlation propagation |
url | http://journal.frontiersin.org/Journal/10.3389/fncom.2014.00053/full |
work_keys_str_mv | AT florenceikleberg excitatoryandinhibitorystdpjointlytunefeedforwardneuralcircuitstoselectivelypropagatecorrelatedspikingactivity AT tomokiefukai excitatoryandinhibitorystdpjointlytunefeedforwardneuralcircuitstoselectivelypropagatecorrelatedspikingactivity AT matthieuegilson excitatoryandinhibitorystdpjointlytunefeedforwardneuralcircuitstoselectivelypropagatecorrelatedspikingactivity |