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Burst Firing Enhances Neural Output Correlation
Neurons communicate and transmit information predominantly through spikes. Given that experimentally observed neural spike trains in a variety of brain areas can be highly correlated, it is important to investigate how neurons process correlated inputs. Most previous work in this area studied the pr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860405/ https://www.ncbi.nlm.nih.gov/pubmed/27242499 http://dx.doi.org/10.3389/fncom.2016.00042 |
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author | Chan, Ho Ka Yang, Dong-Ping Zhou, Changsong Nowotny, Thomas |
author_facet | Chan, Ho Ka Yang, Dong-Ping Zhou, Changsong Nowotny, Thomas |
author_sort | Chan, Ho Ka |
collection | PubMed |
description | Neurons communicate and transmit information predominantly through spikes. Given that experimentally observed neural spike trains in a variety of brain areas can be highly correlated, it is important to investigate how neurons process correlated inputs. Most previous work in this area studied the problem of correlation transfer analytically by making significant simplifications on neural dynamics. Temporal correlation between inputs that arises from synaptic filtering, for instance, is often ignored when assuming that an input spike can at most generate one output spike. Through numerical simulations of a pair of leaky integrate-and-fire (LIF) neurons receiving correlated inputs, we demonstrate that neurons in the presence of synaptic filtering by slow synapses exhibit strong output correlations. We then show that burst firing plays a central role in enhancing output correlations, which can explain the above-mentioned observation because synaptic filtering induces bursting. The observed changes of correlations are mostly on a long time scale. Our results suggest that other features affecting the prevalence of neural burst firing in biological neurons, e.g., adaptive spiking mechanisms, may play an important role in modulating the overall level of correlations in neural networks. |
format | Online Article Text |
id | pubmed-4860405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48604052016-05-30 Burst Firing Enhances Neural Output Correlation Chan, Ho Ka Yang, Dong-Ping Zhou, Changsong Nowotny, Thomas Front Comput Neurosci Neuroscience Neurons communicate and transmit information predominantly through spikes. Given that experimentally observed neural spike trains in a variety of brain areas can be highly correlated, it is important to investigate how neurons process correlated inputs. Most previous work in this area studied the problem of correlation transfer analytically by making significant simplifications on neural dynamics. Temporal correlation between inputs that arises from synaptic filtering, for instance, is often ignored when assuming that an input spike can at most generate one output spike. Through numerical simulations of a pair of leaky integrate-and-fire (LIF) neurons receiving correlated inputs, we demonstrate that neurons in the presence of synaptic filtering by slow synapses exhibit strong output correlations. We then show that burst firing plays a central role in enhancing output correlations, which can explain the above-mentioned observation because synaptic filtering induces bursting. The observed changes of correlations are mostly on a long time scale. Our results suggest that other features affecting the prevalence of neural burst firing in biological neurons, e.g., adaptive spiking mechanisms, may play an important role in modulating the overall level of correlations in neural networks. Frontiers Media S.A. 2016-05-09 /pmc/articles/PMC4860405/ /pubmed/27242499 http://dx.doi.org/10.3389/fncom.2016.00042 Text en Copyright © 2016 Chan, Yang, Zhou and Nowotny. http://creativecommons.org/licenses/by/4.0/ 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 Chan, Ho Ka Yang, Dong-Ping Zhou, Changsong Nowotny, Thomas Burst Firing Enhances Neural Output Correlation |
title | Burst Firing Enhances Neural Output Correlation |
title_full | Burst Firing Enhances Neural Output Correlation |
title_fullStr | Burst Firing Enhances Neural Output Correlation |
title_full_unstemmed | Burst Firing Enhances Neural Output Correlation |
title_short | Burst Firing Enhances Neural Output Correlation |
title_sort | burst firing enhances neural output correlation |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860405/ https://www.ncbi.nlm.nih.gov/pubmed/27242499 http://dx.doi.org/10.3389/fncom.2016.00042 |
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