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A spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands

Single-unit recordings suggest that the midbrain superior colliculus (SC) acts as an optimal controller for saccadic gaze shifts. The SC is proposed to be the site within the visuomotor system where the nonlinear spatial-to-temporal transformation is carried out: the population encodes the intended...

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Autores principales: Kasap, Bahadir, van Opstal, A. John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5506246/
https://www.ncbi.nlm.nih.gov/pubmed/28528360
http://dx.doi.org/10.1007/s00422-017-0719-9
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author Kasap, Bahadir
van Opstal, A. John
author_facet Kasap, Bahadir
van Opstal, A. John
author_sort Kasap, Bahadir
collection PubMed
description Single-unit recordings suggest that the midbrain superior colliculus (SC) acts as an optimal controller for saccadic gaze shifts. The SC is proposed to be the site within the visuomotor system where the nonlinear spatial-to-temporal transformation is carried out: the population encodes the intended saccade vector by its location in the motor map (spatial), and its trajectory and velocity by the distribution of firing rates (temporal). The neurons’ burst profiles vary systematically with their anatomical positions and intended saccade vectors, to account for the nonlinear main-sequence kinematics of saccades. Yet, the underlying collicular mechanisms that could result in these firing patterns are inaccessible to current neurobiological techniques. Here, we propose a simple spiking neural network model that reproduces the spike trains of saccade-related cells in the intermediate and deep SC layers during saccades. The model assumes that SC neurons have distinct biophysical properties for spike generation that depend on their anatomical position in combination with a center–surround lateral connectivity. Both factors are needed to account for the observed firing patterns. Our model offers a basis for neuronal algorithms for spatiotemporal transformations and bio-inspired optimal controllers.
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spelling pubmed-55062462017-07-27 A spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands Kasap, Bahadir van Opstal, A. John Biol Cybern Original Article Single-unit recordings suggest that the midbrain superior colliculus (SC) acts as an optimal controller for saccadic gaze shifts. The SC is proposed to be the site within the visuomotor system where the nonlinear spatial-to-temporal transformation is carried out: the population encodes the intended saccade vector by its location in the motor map (spatial), and its trajectory and velocity by the distribution of firing rates (temporal). The neurons’ burst profiles vary systematically with their anatomical positions and intended saccade vectors, to account for the nonlinear main-sequence kinematics of saccades. Yet, the underlying collicular mechanisms that could result in these firing patterns are inaccessible to current neurobiological techniques. Here, we propose a simple spiking neural network model that reproduces the spike trains of saccade-related cells in the intermediate and deep SC layers during saccades. The model assumes that SC neurons have distinct biophysical properties for spike generation that depend on their anatomical position in combination with a center–surround lateral connectivity. Both factors are needed to account for the observed firing patterns. Our model offers a basis for neuronal algorithms for spatiotemporal transformations and bio-inspired optimal controllers. Springer Berlin Heidelberg 2017-05-20 2017 /pmc/articles/PMC5506246/ /pubmed/28528360 http://dx.doi.org/10.1007/s00422-017-0719-9 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 Original Article
Kasap, Bahadir
van Opstal, A. John
A spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands
title A spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands
title_full A spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands
title_fullStr A spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands
title_full_unstemmed A spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands
title_short A spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands
title_sort spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5506246/
https://www.ncbi.nlm.nih.gov/pubmed/28528360
http://dx.doi.org/10.1007/s00422-017-0719-9
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