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Dual STDP processes at Purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements

Saccadic eye-movements play a crucial role in visuo-motor control by allowing rapid foveation onto new targets. However, the neural processes governing saccades adaptation are not fully understood. Saccades, due to the short-time of execution (20–100 ms) and the absence of sensory information for on...

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Autores principales: Fruzzetti, Lorenzo, Kalidindi, Hari Teja, Antonietti, Alberto, Alessandro, Cristiano, Geminiani, Alice, Casellato, Claudia, Falotico, Egidio, D’Angelo, Egidio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9565489/
https://www.ncbi.nlm.nih.gov/pubmed/36194625
http://dx.doi.org/10.1371/journal.pcbi.1010564
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author Fruzzetti, Lorenzo
Kalidindi, Hari Teja
Antonietti, Alberto
Alessandro, Cristiano
Geminiani, Alice
Casellato, Claudia
Falotico, Egidio
D’Angelo, Egidio
author_facet Fruzzetti, Lorenzo
Kalidindi, Hari Teja
Antonietti, Alberto
Alessandro, Cristiano
Geminiani, Alice
Casellato, Claudia
Falotico, Egidio
D’Angelo, Egidio
author_sort Fruzzetti, Lorenzo
collection PubMed
description Saccadic eye-movements play a crucial role in visuo-motor control by allowing rapid foveation onto new targets. However, the neural processes governing saccades adaptation are not fully understood. Saccades, due to the short-time of execution (20–100 ms) and the absence of sensory information for online feedback control, must be controlled in a ballistic manner. Incomplete measurements of the movement trajectory, such as the visual endpoint error, are supposedly used to form internal predictions about the movement kinematics resulting in predictive control. In order to characterize the synaptic and neural circuit mechanisms underlying predictive saccadic control, we have reconstructed the saccadic system in a digital controller embedding a spiking neural network of the cerebellum with spike timing-dependent plasticity (STDP) rules driving parallel fiber—Purkinje cell long-term potentiation and depression (LTP and LTD). This model implements a control policy based on a dual plasticity mechanism, resulting in the identification of the roles of LTP and LTD in regulating the overall quality of saccade kinematics: it turns out that LTD increases the accuracy by decreasing visual error and LTP increases the peak speed. The control policy also required cerebellar PCs to be divided into two subpopulations, characterized by burst or pause responses. To our knowledge, this is the first model that explains in mechanistic terms the visual error and peak speed regulation of ballistic eye movements in forward mode exploiting spike-timing to regulate firing in different populations of the neuronal network. This elementary model of saccades could be extended and applied to other more complex cases in which single jerks are concatenated to compose articulated and coordinated movements.
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spelling pubmed-95654892022-10-15 Dual STDP processes at Purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements Fruzzetti, Lorenzo Kalidindi, Hari Teja Antonietti, Alberto Alessandro, Cristiano Geminiani, Alice Casellato, Claudia Falotico, Egidio D’Angelo, Egidio PLoS Comput Biol Research Article Saccadic eye-movements play a crucial role in visuo-motor control by allowing rapid foveation onto new targets. However, the neural processes governing saccades adaptation are not fully understood. Saccades, due to the short-time of execution (20–100 ms) and the absence of sensory information for online feedback control, must be controlled in a ballistic manner. Incomplete measurements of the movement trajectory, such as the visual endpoint error, are supposedly used to form internal predictions about the movement kinematics resulting in predictive control. In order to characterize the synaptic and neural circuit mechanisms underlying predictive saccadic control, we have reconstructed the saccadic system in a digital controller embedding a spiking neural network of the cerebellum with spike timing-dependent plasticity (STDP) rules driving parallel fiber—Purkinje cell long-term potentiation and depression (LTP and LTD). This model implements a control policy based on a dual plasticity mechanism, resulting in the identification of the roles of LTP and LTD in regulating the overall quality of saccade kinematics: it turns out that LTD increases the accuracy by decreasing visual error and LTP increases the peak speed. The control policy also required cerebellar PCs to be divided into two subpopulations, characterized by burst or pause responses. To our knowledge, this is the first model that explains in mechanistic terms the visual error and peak speed regulation of ballistic eye movements in forward mode exploiting spike-timing to regulate firing in different populations of the neuronal network. This elementary model of saccades could be extended and applied to other more complex cases in which single jerks are concatenated to compose articulated and coordinated movements. Public Library of Science 2022-10-04 /pmc/articles/PMC9565489/ /pubmed/36194625 http://dx.doi.org/10.1371/journal.pcbi.1010564 Text en © 2022 Fruzzetti et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fruzzetti, Lorenzo
Kalidindi, Hari Teja
Antonietti, Alberto
Alessandro, Cristiano
Geminiani, Alice
Casellato, Claudia
Falotico, Egidio
D’Angelo, Egidio
Dual STDP processes at Purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements
title Dual STDP processes at Purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements
title_full Dual STDP processes at Purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements
title_fullStr Dual STDP processes at Purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements
title_full_unstemmed Dual STDP processes at Purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements
title_short Dual STDP processes at Purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements
title_sort dual stdp processes at purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9565489/
https://www.ncbi.nlm.nih.gov/pubmed/36194625
http://dx.doi.org/10.1371/journal.pcbi.1010564
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