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A unifying theory of synaptic long-term plasticity based on a sparse distribution of synaptic strength

Long-term synaptic plasticity is fundamental to learning and network function. It has been studied under various induction protocols and depends on firing rates, membrane voltage, and precise timing of action potentials. These protocols show different facets of a common underlying mechanism but they...

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Autores principales: Krieg, Daniel, Triesch, Jochen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941589/
https://www.ncbi.nlm.nih.gov/pubmed/24624080
http://dx.doi.org/10.3389/fnsyn.2014.00003
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author Krieg, Daniel
Triesch, Jochen
author_facet Krieg, Daniel
Triesch, Jochen
author_sort Krieg, Daniel
collection PubMed
description Long-term synaptic plasticity is fundamental to learning and network function. It has been studied under various induction protocols and depends on firing rates, membrane voltage, and precise timing of action potentials. These protocols show different facets of a common underlying mechanism but they are mostly modeled as distinct phenomena. Here, we show that all of these different dependencies can be explained from a single computational principle. The objective is a sparse distribution of excitatory synaptic strength, which may help to reduce metabolic costs associated with synaptic transmission. Based on this objective we derive a stochastic gradient ascent learning rule which is of differential-Hebbian type. It is formulated in biophysical quantities and can be related to current mechanistic theories of synaptic plasticity. The learning rule accounts for experimental findings from all major induction protocols and explains a classic phenomenon of metaplasticity. Furthermore, our model predicts the existence of metaplasticity for spike-timing-dependent plasticity Thus, we provide a theory of long-term synaptic plasticity that unifies different induction protocols and provides a connection between functional and mechanistic levels of description.
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spelling pubmed-39415892014-03-12 A unifying theory of synaptic long-term plasticity based on a sparse distribution of synaptic strength Krieg, Daniel Triesch, Jochen Front Synaptic Neurosci Neuroscience Long-term synaptic plasticity is fundamental to learning and network function. It has been studied under various induction protocols and depends on firing rates, membrane voltage, and precise timing of action potentials. These protocols show different facets of a common underlying mechanism but they are mostly modeled as distinct phenomena. Here, we show that all of these different dependencies can be explained from a single computational principle. The objective is a sparse distribution of excitatory synaptic strength, which may help to reduce metabolic costs associated with synaptic transmission. Based on this objective we derive a stochastic gradient ascent learning rule which is of differential-Hebbian type. It is formulated in biophysical quantities and can be related to current mechanistic theories of synaptic plasticity. The learning rule accounts for experimental findings from all major induction protocols and explains a classic phenomenon of metaplasticity. Furthermore, our model predicts the existence of metaplasticity for spike-timing-dependent plasticity Thus, we provide a theory of long-term synaptic plasticity that unifies different induction protocols and provides a connection between functional and mechanistic levels of description. Frontiers Media S.A. 2014-03-04 /pmc/articles/PMC3941589/ /pubmed/24624080 http://dx.doi.org/10.3389/fnsyn.2014.00003 Text en Copyright © 2014 Krieg and Triesch. 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
Krieg, Daniel
Triesch, Jochen
A unifying theory of synaptic long-term plasticity based on a sparse distribution of synaptic strength
title A unifying theory of synaptic long-term plasticity based on a sparse distribution of synaptic strength
title_full A unifying theory of synaptic long-term plasticity based on a sparse distribution of synaptic strength
title_fullStr A unifying theory of synaptic long-term plasticity based on a sparse distribution of synaptic strength
title_full_unstemmed A unifying theory of synaptic long-term plasticity based on a sparse distribution of synaptic strength
title_short A unifying theory of synaptic long-term plasticity based on a sparse distribution of synaptic strength
title_sort unifying theory of synaptic long-term plasticity based on a sparse distribution of synaptic strength
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941589/
https://www.ncbi.nlm.nih.gov/pubmed/24624080
http://dx.doi.org/10.3389/fnsyn.2014.00003
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