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Bursts and Isolated Spikes Code for Opposite Movement Directions in Midbrain Electrosensory Neurons

Directional selectivity, in which neurons respond strongly to an object moving in a given direction but weakly or not at all to the same object moving in the opposite direction, is a crucial computation that is thought to provide a neural correlate of motion perception. However, directional selectiv...

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Autores principales: Khosravi-Hashemi, Navid, Chacron, Maurice J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386997/
https://www.ncbi.nlm.nih.gov/pubmed/22768279
http://dx.doi.org/10.1371/journal.pone.0040339
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author Khosravi-Hashemi, Navid
Chacron, Maurice J.
author_facet Khosravi-Hashemi, Navid
Chacron, Maurice J.
author_sort Khosravi-Hashemi, Navid
collection PubMed
description Directional selectivity, in which neurons respond strongly to an object moving in a given direction but weakly or not at all to the same object moving in the opposite direction, is a crucial computation that is thought to provide a neural correlate of motion perception. However, directional selectivity has been traditionally quantified by using the full spike train, which does not take into account particular action potential patterns. We investigated how different action potential patterns, namely bursts (i.e. packets of action potentials followed by quiescence) and isolated spikes, contribute to movement direction coding in a mathematical model of midbrain electrosensory neurons. We found that bursts and isolated spikes could be selectively elicited when the same object moved in opposite directions. In particular, it was possible to find parameter values for which our model neuron did not display directional selectivity when the full spike train was considered but displayed strong directional selectivity when bursts or isolated spikes were instead considered. Further analysis of our model revealed that an intrinsic burst mechanism based on subthreshold T-type calcium channels was not required to observe parameter regimes for which bursts and isolated spikes code for opposite movement directions. However, this burst mechanism enhanced the range of parameter values for which such regimes were observed. Experimental recordings from midbrain neurons confirmed our modeling prediction that bursts and isolated spikes can indeed code for opposite movement directions. Finally, we quantified the performance of a plausible neural circuit and found that it could respond more or less selectively to isolated spikes for a wide range of parameter values when compared with an interspike interval threshold. Our results thus show for the first time that different action potential patterns can differentially encode movement and that traditional measures of directional selectivity need to be revised in such cases.
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spelling pubmed-33869972012-07-05 Bursts and Isolated Spikes Code for Opposite Movement Directions in Midbrain Electrosensory Neurons Khosravi-Hashemi, Navid Chacron, Maurice J. PLoS One Research Article Directional selectivity, in which neurons respond strongly to an object moving in a given direction but weakly or not at all to the same object moving in the opposite direction, is a crucial computation that is thought to provide a neural correlate of motion perception. However, directional selectivity has been traditionally quantified by using the full spike train, which does not take into account particular action potential patterns. We investigated how different action potential patterns, namely bursts (i.e. packets of action potentials followed by quiescence) and isolated spikes, contribute to movement direction coding in a mathematical model of midbrain electrosensory neurons. We found that bursts and isolated spikes could be selectively elicited when the same object moved in opposite directions. In particular, it was possible to find parameter values for which our model neuron did not display directional selectivity when the full spike train was considered but displayed strong directional selectivity when bursts or isolated spikes were instead considered. Further analysis of our model revealed that an intrinsic burst mechanism based on subthreshold T-type calcium channels was not required to observe parameter regimes for which bursts and isolated spikes code for opposite movement directions. However, this burst mechanism enhanced the range of parameter values for which such regimes were observed. Experimental recordings from midbrain neurons confirmed our modeling prediction that bursts and isolated spikes can indeed code for opposite movement directions. Finally, we quantified the performance of a plausible neural circuit and found that it could respond more or less selectively to isolated spikes for a wide range of parameter values when compared with an interspike interval threshold. Our results thus show for the first time that different action potential patterns can differentially encode movement and that traditional measures of directional selectivity need to be revised in such cases. Public Library of Science 2012-06-29 /pmc/articles/PMC3386997/ /pubmed/22768279 http://dx.doi.org/10.1371/journal.pone.0040339 Text en Khosravi-Hashemi, Chacron. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Khosravi-Hashemi, Navid
Chacron, Maurice J.
Bursts and Isolated Spikes Code for Opposite Movement Directions in Midbrain Electrosensory Neurons
title Bursts and Isolated Spikes Code for Opposite Movement Directions in Midbrain Electrosensory Neurons
title_full Bursts and Isolated Spikes Code for Opposite Movement Directions in Midbrain Electrosensory Neurons
title_fullStr Bursts and Isolated Spikes Code for Opposite Movement Directions in Midbrain Electrosensory Neurons
title_full_unstemmed Bursts and Isolated Spikes Code for Opposite Movement Directions in Midbrain Electrosensory Neurons
title_short Bursts and Isolated Spikes Code for Opposite Movement Directions in Midbrain Electrosensory Neurons
title_sort bursts and isolated spikes code for opposite movement directions in midbrain electrosensory neurons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386997/
https://www.ncbi.nlm.nih.gov/pubmed/22768279
http://dx.doi.org/10.1371/journal.pone.0040339
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