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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2021
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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. |
format | Online Article Text |
id | pubmed-7986529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
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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