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Targeted cortical reorganization using optogenetics in non-human primates
Brain stimulation modulates the excitability of neural circuits and drives neuroplasticity. While the local effects of stimulation have been an active area of investigation, the effects on large-scale networks remain largely unexplored. We studied stimulation-induced changes in network dynamics in t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5986269/ https://www.ncbi.nlm.nih.gov/pubmed/29809133 http://dx.doi.org/10.7554/eLife.31034 |
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author | Yazdan-Shahmorad, Azadeh Silversmith, Daniel B Kharazia, Viktor Sabes, Philip N |
author_facet | Yazdan-Shahmorad, Azadeh Silversmith, Daniel B Kharazia, Viktor Sabes, Philip N |
author_sort | Yazdan-Shahmorad, Azadeh |
collection | PubMed |
description | Brain stimulation modulates the excitability of neural circuits and drives neuroplasticity. While the local effects of stimulation have been an active area of investigation, the effects on large-scale networks remain largely unexplored. We studied stimulation-induced changes in network dynamics in two macaques. A large-scale optogenetic interface enabled simultaneous stimulation of excitatory neurons and electrocorticographic recording across primary somatosensory (S1) and motor (M1) cortex (Yazdan-Shahmorad et al., 2016). We tracked two measures of network connectivity, the network response to focal stimulation and the baseline coherence between pairs of electrodes; these were strongly correlated before stimulation. Within minutes, stimulation in S1 or M1 significantly strengthened the gross functional connectivity between these areas. At a finer scale, stimulation led to heterogeneous connectivity changes across the network. These changes reflected the correlations introduced by stimulation-evoked activity, consistent with Hebbian plasticity models. This work extends Hebbian plasticity models to large-scale circuits, with significant implications for stimulation-based neurorehabilitation. |
format | Online Article Text |
id | pubmed-5986269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59862692018-06-06 Targeted cortical reorganization using optogenetics in non-human primates Yazdan-Shahmorad, Azadeh Silversmith, Daniel B Kharazia, Viktor Sabes, Philip N eLife Neuroscience Brain stimulation modulates the excitability of neural circuits and drives neuroplasticity. While the local effects of stimulation have been an active area of investigation, the effects on large-scale networks remain largely unexplored. We studied stimulation-induced changes in network dynamics in two macaques. A large-scale optogenetic interface enabled simultaneous stimulation of excitatory neurons and electrocorticographic recording across primary somatosensory (S1) and motor (M1) cortex (Yazdan-Shahmorad et al., 2016). We tracked two measures of network connectivity, the network response to focal stimulation and the baseline coherence between pairs of electrodes; these were strongly correlated before stimulation. Within minutes, stimulation in S1 or M1 significantly strengthened the gross functional connectivity between these areas. At a finer scale, stimulation led to heterogeneous connectivity changes across the network. These changes reflected the correlations introduced by stimulation-evoked activity, consistent with Hebbian plasticity models. This work extends Hebbian plasticity models to large-scale circuits, with significant implications for stimulation-based neurorehabilitation. eLife Sciences Publications, Ltd 2018-05-29 /pmc/articles/PMC5986269/ /pubmed/29809133 http://dx.doi.org/10.7554/eLife.31034 Text en © 2018, Yazdan-Shahmorad et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Yazdan-Shahmorad, Azadeh Silversmith, Daniel B Kharazia, Viktor Sabes, Philip N Targeted cortical reorganization using optogenetics in non-human primates |
title | Targeted cortical reorganization using optogenetics in non-human primates |
title_full | Targeted cortical reorganization using optogenetics in non-human primates |
title_fullStr | Targeted cortical reorganization using optogenetics in non-human primates |
title_full_unstemmed | Targeted cortical reorganization using optogenetics in non-human primates |
title_short | Targeted cortical reorganization using optogenetics in non-human primates |
title_sort | targeted cortical reorganization using optogenetics in non-human primates |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5986269/ https://www.ncbi.nlm.nih.gov/pubmed/29809133 http://dx.doi.org/10.7554/eLife.31034 |
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