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Double Stimulation in a Spiking Neural Network Model of the Midbrain Superior Colliculus

The midbrain superior colliculus (SC) is a crucial sensorimotor interface in the generation of rapid saccadic gaze shifts. For every saccade it recruits a large population of cells in its vectorial motor map. Supra-threshold electrical microstimulation in the SC reveals that the stimulated site prod...

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Autores principales: Kasap, Bahadir, van Opstal, A. John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751081/
https://www.ncbi.nlm.nih.gov/pubmed/31534950
http://dx.doi.org/10.3389/fams.2018.00047
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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 The midbrain superior colliculus (SC) is a crucial sensorimotor interface in the generation of rapid saccadic gaze shifts. For every saccade it recruits a large population of cells in its vectorial motor map. Supra-threshold electrical microstimulation in the SC reveals that the stimulated site produces the saccade vector specified by the motor map. Electrically evoked saccades (E-saccades) have kinematic properties that strongly resemble natural, visual-evoked saccades (V-saccades), with little influence of the stimulation parameters. Moreover, synchronous stimulation at two sites yields eye movements that resemble a weighted vector average of the individual stimulation effects. Single-unit recordings have indicated that the SC population acts as a vectorial pulse generator by specifying the instantaneous gaze-kinematics through dynamic summation of the movement effects of all SC spike trains. But how to reconcile the a-specific stimulation pulses with these intricate saccade properties? We recently developed a spiking neural network model of the SC, in which microstimulation initially activates a relatively small set of (~50) neurons around the electrode tip, which subsequently sets up a large population response (~5,000 neurons) through lateral synaptic interactions. Single-site microstimulation in this network thus produces the saccade properties and firing rate profiles as seen in single-unit recording experiments. We here show that this mechanism also accounts for many results of simultaneous double stimulation at different SC sites. The resulting E-saccade trajectories resemble a weighted average of the single-site effects, in which stimulus current strength of the electrode pulses serve as weighting factors. We discuss under which conditions the network produces effects that deviate from experimental results.
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spelling pubmed-67510812019-09-18 Double Stimulation in a Spiking Neural Network Model of the Midbrain Superior Colliculus Kasap, Bahadir van Opstal, A. John Front Appl Math Stat Article The midbrain superior colliculus (SC) is a crucial sensorimotor interface in the generation of rapid saccadic gaze shifts. For every saccade it recruits a large population of cells in its vectorial motor map. Supra-threshold electrical microstimulation in the SC reveals that the stimulated site produces the saccade vector specified by the motor map. Electrically evoked saccades (E-saccades) have kinematic properties that strongly resemble natural, visual-evoked saccades (V-saccades), with little influence of the stimulation parameters. Moreover, synchronous stimulation at two sites yields eye movements that resemble a weighted vector average of the individual stimulation effects. Single-unit recordings have indicated that the SC population acts as a vectorial pulse generator by specifying the instantaneous gaze-kinematics through dynamic summation of the movement effects of all SC spike trains. But how to reconcile the a-specific stimulation pulses with these intricate saccade properties? We recently developed a spiking neural network model of the SC, in which microstimulation initially activates a relatively small set of (~50) neurons around the electrode tip, which subsequently sets up a large population response (~5,000 neurons) through lateral synaptic interactions. Single-site microstimulation in this network thus produces the saccade properties and firing rate profiles as seen in single-unit recording experiments. We here show that this mechanism also accounts for many results of simultaneous double stimulation at different SC sites. The resulting E-saccade trajectories resemble a weighted average of the single-site effects, in which stimulus current strength of the electrode pulses serve as weighting factors. We discuss under which conditions the network produces effects that deviate from experimental results. 2018-10-09 2018 /pmc/articles/PMC6751081/ /pubmed/31534950 http://dx.doi.org/10.3389/fams.2018.00047 Text en 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) (http://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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 Article
Kasap, Bahadir
van Opstal, A. John
Double Stimulation in a Spiking Neural Network Model of the Midbrain Superior Colliculus
title Double Stimulation in a Spiking Neural Network Model of the Midbrain Superior Colliculus
title_full Double Stimulation in a Spiking Neural Network Model of the Midbrain Superior Colliculus
title_fullStr Double Stimulation in a Spiking Neural Network Model of the Midbrain Superior Colliculus
title_full_unstemmed Double Stimulation in a Spiking Neural Network Model of the Midbrain Superior Colliculus
title_short Double Stimulation in a Spiking Neural Network Model of the Midbrain Superior Colliculus
title_sort double stimulation in a spiking neural network model of the midbrain superior colliculus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751081/
https://www.ncbi.nlm.nih.gov/pubmed/31534950
http://dx.doi.org/10.3389/fams.2018.00047
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