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Transmission of temporally correlated spike trains through synapses with short-term depression

Short-term synaptic depression, caused by depletion of releasable neurotransmitter, modulates the strength of neuronal connections in a history-dependent manner. Quantifying the statistics of synaptic transmission requires stochastic models that link probabilistic neurotransmitter release with presy...

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Detalles Bibliográficos
Autores principales: Bird, Alex D., Richardson, Magnus J. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039054/
https://www.ncbi.nlm.nih.gov/pubmed/29933363
http://dx.doi.org/10.1371/journal.pcbi.1006232
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author Bird, Alex D.
Richardson, Magnus J. E.
author_facet Bird, Alex D.
Richardson, Magnus J. E.
author_sort Bird, Alex D.
collection PubMed
description Short-term synaptic depression, caused by depletion of releasable neurotransmitter, modulates the strength of neuronal connections in a history-dependent manner. Quantifying the statistics of synaptic transmission requires stochastic models that link probabilistic neurotransmitter release with presynaptic spike-train statistics. Common approaches are to model the presynaptic spike train as either regular or a memory-less Poisson process: few analytical results are available that describe depressing synapses when the afferent spike train has more complex, temporally correlated statistics such as bursts. Here we present a series of analytical results—from vesicle release-site occupancy statistics, via neurotransmitter release, to the post-synaptic voltage mean and variance—for depressing synapses driven by correlated presynaptic spike trains. The class of presynaptic drive considered is that fully characterised by the inter-spike-interval distribution and encompasses a broad range of models used for neuronal circuit and network analyses, such as integrate-and-fire models with a complete post-spike reset and receiving sufficiently short-time correlated drive. We further demonstrate that the derived post-synaptic voltage mean and variance allow for a simple and accurate approximation of the firing rate of the post-synaptic neuron, using the exponential integrate-and-fire model as an example. These results extend the level of biological detail included in models of synaptic transmission and will allow for the incorporation of more complex and physiologically relevant firing patterns into future studies of neuronal networks.
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spelling pubmed-60390542018-07-19 Transmission of temporally correlated spike trains through synapses with short-term depression Bird, Alex D. Richardson, Magnus J. E. PLoS Comput Biol Research Article Short-term synaptic depression, caused by depletion of releasable neurotransmitter, modulates the strength of neuronal connections in a history-dependent manner. Quantifying the statistics of synaptic transmission requires stochastic models that link probabilistic neurotransmitter release with presynaptic spike-train statistics. Common approaches are to model the presynaptic spike train as either regular or a memory-less Poisson process: few analytical results are available that describe depressing synapses when the afferent spike train has more complex, temporally correlated statistics such as bursts. Here we present a series of analytical results—from vesicle release-site occupancy statistics, via neurotransmitter release, to the post-synaptic voltage mean and variance—for depressing synapses driven by correlated presynaptic spike trains. The class of presynaptic drive considered is that fully characterised by the inter-spike-interval distribution and encompasses a broad range of models used for neuronal circuit and network analyses, such as integrate-and-fire models with a complete post-spike reset and receiving sufficiently short-time correlated drive. We further demonstrate that the derived post-synaptic voltage mean and variance allow for a simple and accurate approximation of the firing rate of the post-synaptic neuron, using the exponential integrate-and-fire model as an example. These results extend the level of biological detail included in models of synaptic transmission and will allow for the incorporation of more complex and physiologically relevant firing patterns into future studies of neuronal networks. Public Library of Science 2018-06-22 /pmc/articles/PMC6039054/ /pubmed/29933363 http://dx.doi.org/10.1371/journal.pcbi.1006232 Text en © 2018 Bird, Richardson http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bird, Alex D.
Richardson, Magnus J. E.
Transmission of temporally correlated spike trains through synapses with short-term depression
title Transmission of temporally correlated spike trains through synapses with short-term depression
title_full Transmission of temporally correlated spike trains through synapses with short-term depression
title_fullStr Transmission of temporally correlated spike trains through synapses with short-term depression
title_full_unstemmed Transmission of temporally correlated spike trains through synapses with short-term depression
title_short Transmission of temporally correlated spike trains through synapses with short-term depression
title_sort transmission of temporally correlated spike trains through synapses with short-term depression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039054/
https://www.ncbi.nlm.nih.gov/pubmed/29933363
http://dx.doi.org/10.1371/journal.pcbi.1006232
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