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An Integrate-and-Fire Spiking Neural Network Model Simulating Artificially Induced Cortical Plasticity

We describe an integrate-and-fire (IF) spiking neural network that incorporates spike-timing-dependent plasticity (STDP) and simulates the experimental outcomes of four different conditioning protocols that produce cortical plasticity. The original conditioning experiments were performed in freely m...

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Autores principales: Shupe, Larry, Fetz, Eberhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986529/
https://www.ncbi.nlm.nih.gov/pubmed/33632810
http://dx.doi.org/10.1523/ENEURO.0333-20.2021
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author Shupe, Larry
Fetz, Eberhard
author_facet Shupe, Larry
Fetz, Eberhard
author_sort Shupe, Larry
collection PubMed
description We describe an integrate-and-fire (IF) spiking neural network that incorporates spike-timing-dependent plasticity (STDP) and simulates the experimental outcomes of four different conditioning protocols that produce cortical plasticity. The original conditioning experiments were performed in freely moving non-human primates (NHPs) with an autonomous head-fixed bidirectional brain-computer interface (BCI). Three protocols involved closed-loop stimulation triggered from (1) spike activity of single cortical neurons, (2) electromyographic (EMG) activity from forearm muscles, and (3) cycles of spontaneous cortical beta activity. A fourth protocol involved open-loop delivery of pairs of stimuli at neighboring cortical sites. The IF network that replicates the experimental results consists of 360 units with simulated membrane potentials produced by synaptic inputs and triggering a spike when reaching threshold. The 240 cortical units produce either excitatory or inhibitory postsynaptic potentials (PSPs) in their target units. In addition to the experimentally observed conditioning effects, the model also allows computation of underlying network behavior not originally documented. Furthermore, the model makes predictions about outcomes from protocols not yet investigated, including spike-triggered inhibition, γ-triggered stimulation and disynaptic conditioning. The success of the simulations suggests that a simple voltage-based IF model incorporating STDP can capture the essential mechanisms mediating targeted plasticity with closed-loop stimulation.
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spelling pubmed-79865292021-03-23 An Integrate-and-Fire Spiking Neural Network Model Simulating Artificially Induced Cortical Plasticity Shupe, Larry Fetz, Eberhard eNeuro Research Article: New Research We describe an integrate-and-fire (IF) spiking neural network that incorporates spike-timing-dependent plasticity (STDP) and simulates the experimental outcomes of four different conditioning protocols that produce cortical plasticity. The original conditioning experiments were performed in freely moving non-human primates (NHPs) with an autonomous head-fixed bidirectional brain-computer interface (BCI). Three protocols involved closed-loop stimulation triggered from (1) spike activity of single cortical neurons, (2) electromyographic (EMG) activity from forearm muscles, and (3) cycles of spontaneous cortical beta activity. A fourth protocol involved open-loop delivery of pairs of stimuli at neighboring cortical sites. The IF network that replicates the experimental results consists of 360 units with simulated membrane potentials produced by synaptic inputs and triggering a spike when reaching threshold. The 240 cortical units produce either excitatory or inhibitory postsynaptic potentials (PSPs) in their target units. In addition to the experimentally observed conditioning effects, the model also allows computation of underlying network behavior not originally documented. Furthermore, the model makes predictions about outcomes from protocols not yet investigated, including spike-triggered inhibition, γ-triggered stimulation and disynaptic conditioning. The success of the simulations suggests that a simple voltage-based IF model incorporating STDP can capture the essential mechanisms mediating targeted plasticity with closed-loop stimulation. Society for Neuroscience 2021-03-11 /pmc/articles/PMC7986529/ /pubmed/33632810 http://dx.doi.org/10.1523/ENEURO.0333-20.2021 Text en Copyright © 2021 Shupe and Fetz https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: New Research
Shupe, Larry
Fetz, Eberhard
An Integrate-and-Fire Spiking Neural Network Model Simulating Artificially Induced Cortical Plasticity
title An Integrate-and-Fire Spiking Neural Network Model Simulating Artificially Induced Cortical Plasticity
title_full An Integrate-and-Fire Spiking Neural Network Model Simulating Artificially Induced Cortical Plasticity
title_fullStr An Integrate-and-Fire Spiking Neural Network Model Simulating Artificially Induced Cortical Plasticity
title_full_unstemmed An Integrate-and-Fire Spiking Neural Network Model Simulating Artificially Induced Cortical Plasticity
title_short An Integrate-and-Fire Spiking Neural Network Model Simulating Artificially Induced Cortical Plasticity
title_sort integrate-and-fire spiking neural network model simulating artificially induced cortical plasticity
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986529/
https://www.ncbi.nlm.nih.gov/pubmed/33632810
http://dx.doi.org/10.1523/ENEURO.0333-20.2021
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