The spatial structure of stimuli shapes the timescale of correlations in population spiking activity.

Throughout the central nervous system, the timescale over which pairs of neural spike trains are correlated is shaped by stimulus structure and behavioral context. Such shaping is thought to underlie important changes in the neural code, but the neural circuitry responsible is largely unknown. In th...

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Main Authors: Ashok Litwin-Kumar, Maurice J Chacron, Brent Doiron
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Computational Biology
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23028274/?tool=EBI
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spelling doaj-b2cb9ed58f3d49688d1b7bc9ff9096c62021-04-21T15:09:34ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582012-01-0189e100266710.1371/journal.pcbi.1002667The spatial structure of stimuli shapes the timescale of correlations in population spiking activity.Ashok Litwin-KumarMaurice J ChacronBrent DoironThroughout the central nervous system, the timescale over which pairs of neural spike trains are correlated is shaped by stimulus structure and behavioral context. Such shaping is thought to underlie important changes in the neural code, but the neural circuitry responsible is largely unknown. In this study, we investigate a stimulus-induced shaping of pairwise spike train correlations in the electrosensory system of weakly electric fish. Simultaneous single unit recordings of principal electrosensory cells show that an increase in the spatial extent of stimuli increases correlations at short (≈ 10 ms) timescales while simultaneously reducing correlations at long (≈ 100 ms) timescales. A spiking network model of the first two stages of electrosensory processing replicates this correlation shaping, under the assumptions that spatially broad stimuli both saturate feedforward afferent input and recruit an open-loop inhibitory feedback pathway. Our model predictions are experimentally verified using both the natural heterogeneity of the electrosensory system and pharmacological blockade of descending feedback projections. For weak stimuli, linear response analysis of the spiking network shows that the reduction of long timescale correlation for spatially broad stimuli is similar to correlation cancellation mechanisms previously suggested to be operative in mammalian cortex. The mechanism for correlation shaping supports population-level filtering of irrelevant distractor stimuli, thereby enhancing the population response to relevant prey and conspecific communication inputs.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23028274/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Ashok Litwin-Kumar
Maurice J Chacron
Brent Doiron
spellingShingle Ashok Litwin-Kumar
Maurice J Chacron
Brent Doiron
The spatial structure of stimuli shapes the timescale of correlations in population spiking activity.
PLoS Computational Biology
author_facet Ashok Litwin-Kumar
Maurice J Chacron
Brent Doiron
author_sort Ashok Litwin-Kumar
title The spatial structure of stimuli shapes the timescale of correlations in population spiking activity.
title_short The spatial structure of stimuli shapes the timescale of correlations in population spiking activity.
title_full The spatial structure of stimuli shapes the timescale of correlations in population spiking activity.
title_fullStr The spatial structure of stimuli shapes the timescale of correlations in population spiking activity.
title_full_unstemmed The spatial structure of stimuli shapes the timescale of correlations in population spiking activity.
title_sort spatial structure of stimuli shapes the timescale of correlations in population spiking activity.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2012-01-01
description Throughout the central nervous system, the timescale over which pairs of neural spike trains are correlated is shaped by stimulus structure and behavioral context. Such shaping is thought to underlie important changes in the neural code, but the neural circuitry responsible is largely unknown. In this study, we investigate a stimulus-induced shaping of pairwise spike train correlations in the electrosensory system of weakly electric fish. Simultaneous single unit recordings of principal electrosensory cells show that an increase in the spatial extent of stimuli increases correlations at short (≈ 10 ms) timescales while simultaneously reducing correlations at long (≈ 100 ms) timescales. A spiking network model of the first two stages of electrosensory processing replicates this correlation shaping, under the assumptions that spatially broad stimuli both saturate feedforward afferent input and recruit an open-loop inhibitory feedback pathway. Our model predictions are experimentally verified using both the natural heterogeneity of the electrosensory system and pharmacological blockade of descending feedback projections. For weak stimuli, linear response analysis of the spiking network shows that the reduction of long timescale correlation for spatially broad stimuli is similar to correlation cancellation mechanisms previously suggested to be operative in mammalian cortex. The mechanism for correlation shaping supports population-level filtering of irrelevant distractor stimuli, thereby enhancing the population response to relevant prey and conspecific communication inputs.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23028274/?tool=EBI
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