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Theta-specific susceptibility in a model of adaptive synaptic plasticity

Learning and memory formation are processes which are still not fully understood. It is widely believed that synaptic plasticity is the most important neural substrate for both. However, it has been observed that large-scale theta band oscillations in the mammalian brain are beneficial for learning,...

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Autores principales: Albers, Christian, Schmiedt, Joscha T., Pawelzik, Klaus R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835974/
https://www.ncbi.nlm.nih.gov/pubmed/24312047
http://dx.doi.org/10.3389/fncom.2013.00170
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author Albers, Christian
Schmiedt, Joscha T.
Pawelzik, Klaus R.
author_facet Albers, Christian
Schmiedt, Joscha T.
Pawelzik, Klaus R.
author_sort Albers, Christian
collection PubMed
description Learning and memory formation are processes which are still not fully understood. It is widely believed that synaptic plasticity is the most important neural substrate for both. However, it has been observed that large-scale theta band oscillations in the mammalian brain are beneficial for learning, and it is not clear if and how this is linked to synaptic plasticity. Also, the underlying dynamics of synaptic plasticity itself have not been completely uncovered yet, especially for non-linear interactions between multiple spikes. Here, we present a new and simple dynamical model of synaptic plasticity. It incorporates novel contributions to synaptic plasticity including adaptation processes. We test its ability to reproduce non-linear effects on four different data sets of complex spike patterns, and show that the model can be tuned to reproduce the observed synaptic changes in great detail. When subjected to periodically varying firing rates, already linear pair based spike timing dependent plasticity (STDP) predicts a specific susceptibility of synaptic plasticity to pre- and postsynaptic firing rate oscillations in the theta-band. Our model retains this band-pass property, while for high firing rates in the non-linear regime it modifies the specific phase relation required for depression and potentiation. For realistic parameters, maximal synaptic potentiation occurs when the postsynaptic is trailing the presynaptic activity slightly. Anti-phase oscillations tend to depress it. Our results are well in line with experimental findings, providing a straightforward and mechanistic explanation for the importance of theta oscillations for learning.
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spelling pubmed-38359742013-12-05 Theta-specific susceptibility in a model of adaptive synaptic plasticity Albers, Christian Schmiedt, Joscha T. Pawelzik, Klaus R. Front Comput Neurosci Neuroscience Learning and memory formation are processes which are still not fully understood. It is widely believed that synaptic plasticity is the most important neural substrate for both. However, it has been observed that large-scale theta band oscillations in the mammalian brain are beneficial for learning, and it is not clear if and how this is linked to synaptic plasticity. Also, the underlying dynamics of synaptic plasticity itself have not been completely uncovered yet, especially for non-linear interactions between multiple spikes. Here, we present a new and simple dynamical model of synaptic plasticity. It incorporates novel contributions to synaptic plasticity including adaptation processes. We test its ability to reproduce non-linear effects on four different data sets of complex spike patterns, and show that the model can be tuned to reproduce the observed synaptic changes in great detail. When subjected to periodically varying firing rates, already linear pair based spike timing dependent plasticity (STDP) predicts a specific susceptibility of synaptic plasticity to pre- and postsynaptic firing rate oscillations in the theta-band. Our model retains this band-pass property, while for high firing rates in the non-linear regime it modifies the specific phase relation required for depression and potentiation. For realistic parameters, maximal synaptic potentiation occurs when the postsynaptic is trailing the presynaptic activity slightly. Anti-phase oscillations tend to depress it. Our results are well in line with experimental findings, providing a straightforward and mechanistic explanation for the importance of theta oscillations for learning. Frontiers Media S.A. 2013-11-21 /pmc/articles/PMC3835974/ /pubmed/24312047 http://dx.doi.org/10.3389/fncom.2013.00170 Text en Copyright © 2013 Albers, Schmiedt and Pawelzik. 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
Albers, Christian
Schmiedt, Joscha T.
Pawelzik, Klaus R.
Theta-specific susceptibility in a model of adaptive synaptic plasticity
title Theta-specific susceptibility in a model of adaptive synaptic plasticity
title_full Theta-specific susceptibility in a model of adaptive synaptic plasticity
title_fullStr Theta-specific susceptibility in a model of adaptive synaptic plasticity
title_full_unstemmed Theta-specific susceptibility in a model of adaptive synaptic plasticity
title_short Theta-specific susceptibility in a model of adaptive synaptic plasticity
title_sort theta-specific susceptibility in a model of adaptive synaptic plasticity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835974/
https://www.ncbi.nlm.nih.gov/pubmed/24312047
http://dx.doi.org/10.3389/fncom.2013.00170
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