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How does transient signaling input affect the spike timing of postsynaptic neuron near the threshold regime: an analytical study
The noisy threshold regime, where even a small set of presynaptic neurons can significantly affect postsynaptic spike-timing, is suggested as a key requisite for computation in neurons with high variability. It also has been proposed that signals under the noisy conditions are successfully transferr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851711/ https://www.ncbi.nlm.nih.gov/pubmed/29192377 http://dx.doi.org/10.1007/s10827-017-0664-6 |
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author | Shomali, Safura Rashid Ahmadabadi, Majid Nili Shimazaki, Hideaki Rasuli, Seyyed Nader |
author_facet | Shomali, Safura Rashid Ahmadabadi, Majid Nili Shimazaki, Hideaki Rasuli, Seyyed Nader |
author_sort | Shomali, Safura Rashid |
collection | PubMed |
description | The noisy threshold regime, where even a small set of presynaptic neurons can significantly affect postsynaptic spike-timing, is suggested as a key requisite for computation in neurons with high variability. It also has been proposed that signals under the noisy conditions are successfully transferred by a few strong synapses and/or by an assembly of nearly synchronous synaptic activities. We analytically investigate the impact of a transient signaling input on a leaky integrate-and-fire postsynaptic neuron that receives background noise near the threshold regime. The signaling input models a single strong synapse or a set of synchronous synapses, while the background noise represents a lot of weak synapses. We find an analytic solution that explains how the first-passage time (ISI) density is changed by transient signaling input. The analysis allows us to connect properties of the signaling input like spike timing and amplitude with postsynaptic first-passage time density in a noisy environment. Based on the analytic solution, we calculate the Fisher information with respect to the signaling input’s amplitude. For a wide range of amplitudes, we observe a non-monotonic behavior for the Fisher information as a function of background noise. Moreover, Fisher information non-trivially depends on the signaling input’s amplitude; changing the amplitude, we observe one maximum in the high level of the background noise. The single maximum splits into two maximums in the low noise regime. This finding demonstrates the benefit of the analytic solution in investigating signal transfer by neurons. |
format | Online Article Text |
id | pubmed-5851711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-58517112018-03-21 How does transient signaling input affect the spike timing of postsynaptic neuron near the threshold regime: an analytical study Shomali, Safura Rashid Ahmadabadi, Majid Nili Shimazaki, Hideaki Rasuli, Seyyed Nader J Comput Neurosci Article The noisy threshold regime, where even a small set of presynaptic neurons can significantly affect postsynaptic spike-timing, is suggested as a key requisite for computation in neurons with high variability. It also has been proposed that signals under the noisy conditions are successfully transferred by a few strong synapses and/or by an assembly of nearly synchronous synaptic activities. We analytically investigate the impact of a transient signaling input on a leaky integrate-and-fire postsynaptic neuron that receives background noise near the threshold regime. The signaling input models a single strong synapse or a set of synchronous synapses, while the background noise represents a lot of weak synapses. We find an analytic solution that explains how the first-passage time (ISI) density is changed by transient signaling input. The analysis allows us to connect properties of the signaling input like spike timing and amplitude with postsynaptic first-passage time density in a noisy environment. Based on the analytic solution, we calculate the Fisher information with respect to the signaling input’s amplitude. For a wide range of amplitudes, we observe a non-monotonic behavior for the Fisher information as a function of background noise. Moreover, Fisher information non-trivially depends on the signaling input’s amplitude; changing the amplitude, we observe one maximum in the high level of the background noise. The single maximum splits into two maximums in the low noise regime. This finding demonstrates the benefit of the analytic solution in investigating signal transfer by neurons. Springer US 2017-12-01 2018 /pmc/articles/PMC5851711/ /pubmed/29192377 http://dx.doi.org/10.1007/s10827-017-0664-6 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Shomali, Safura Rashid Ahmadabadi, Majid Nili Shimazaki, Hideaki Rasuli, Seyyed Nader How does transient signaling input affect the spike timing of postsynaptic neuron near the threshold regime: an analytical study |
title | How does transient signaling input affect the spike timing of postsynaptic neuron near the threshold regime: an analytical study |
title_full | How does transient signaling input affect the spike timing of postsynaptic neuron near the threshold regime: an analytical study |
title_fullStr | How does transient signaling input affect the spike timing of postsynaptic neuron near the threshold regime: an analytical study |
title_full_unstemmed | How does transient signaling input affect the spike timing of postsynaptic neuron near the threshold regime: an analytical study |
title_short | How does transient signaling input affect the spike timing of postsynaptic neuron near the threshold regime: an analytical study |
title_sort | how does transient signaling input affect the spike timing of postsynaptic neuron near the threshold regime: an analytical study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851711/ https://www.ncbi.nlm.nih.gov/pubmed/29192377 http://dx.doi.org/10.1007/s10827-017-0664-6 |
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