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...
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Online Access: | http://journal.frontiersin.org/Journal/10.3389/fncom.2016.00042/full |
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doaj-9510fca033ee4877bd82e059749999d12020-11-24T22:01:27ZengFrontiers Media S.A.Frontiers in Computational Neuroscience1662-51882016-05-011010.3389/fncom.2016.00042189663Burst firing enhances neural output correlationHo Ka eChan0Ho Ka eChan1Dong-ping eYang2Dong-ping eYang3Changsong eZhou4Thomas eNowotny5University of SussexHong Kong Baptist UniversityUniversity of SydneyHong Kong Baptist UniversityHong Kong Baptist UniversityUniversity of SussexNeurons 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.http://journal.frontiersin.org/Journal/10.3389/fncom.2016.00042/fulladaptationCorrelationburstLeaky integrate-and-fireSynaptic filtering |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ho Ka eChan Ho Ka eChan Dong-ping eYang Dong-ping eYang Changsong eZhou Thomas eNowotny |
spellingShingle |
Ho Ka eChan Ho Ka eChan Dong-ping eYang Dong-ping eYang Changsong eZhou Thomas eNowotny Burst firing enhances neural output correlation Frontiers in Computational Neuroscience adaptation Correlation burst Leaky integrate-and-fire Synaptic filtering |
author_facet |
Ho Ka eChan Ho Ka eChan Dong-ping eYang Dong-ping eYang Changsong eZhou Thomas eNowotny |
author_sort |
Ho Ka eChan |
title |
Burst firing enhances neural output correlation |
title_short |
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_sort |
burst firing enhances neural output correlation |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Computational Neuroscience |
issn |
1662-5188 |
publishDate |
2016-05-01 |
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. |
topic |
adaptation Correlation burst Leaky integrate-and-fire Synaptic filtering |
url |
http://journal.frontiersin.org/Journal/10.3389/fncom.2016.00042/full |
work_keys_str_mv |
AT hokaechan burstfiringenhancesneuraloutputcorrelation AT hokaechan burstfiringenhancesneuraloutputcorrelation AT dongpingeyang burstfiringenhancesneuraloutputcorrelation AT dongpingeyang burstfiringenhancesneuraloutputcorrelation AT changsongezhou burstfiringenhancesneuraloutputcorrelation AT thomasenowotny burstfiringenhancesneuraloutputcorrelation |
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