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Synaptic Plasticity Controls Sensory Responses through Frequency-Dependent Gamma Oscillation Resonance
Synchronized gamma frequency oscillations in neural networks are thought to be important to sensory information processing, and their effects have been intensively studied. Here we describe a mechanism by which the nervous system can readily control gamma oscillation effects, depending selectively o...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936516/ https://www.ncbi.nlm.nih.gov/pubmed/20838581 http://dx.doi.org/10.1371/journal.pcbi.1000927 |
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author | Paik, Se-Bum Glaser, Donald A. |
author_facet | Paik, Se-Bum Glaser, Donald A. |
author_sort | Paik, Se-Bum |
collection | PubMed |
description | Synchronized gamma frequency oscillations in neural networks are thought to be important to sensory information processing, and their effects have been intensively studied. Here we describe a mechanism by which the nervous system can readily control gamma oscillation effects, depending selectively on visual stimuli. Using a model neural network simulation, we found that sensory response in the primary visual cortex is significantly modulated by the resonance between “spontaneous” and “stimulus-driven” oscillations. This gamma resonance can be precisely controlled by the synaptic plasticity of thalamocortical connections, and cortical response is regulated differentially according to the resonance condition. The mechanism produces a selective synchronization between the afferent and downstream neural population. Our simulation results explain experimental observations such as stimulus-dependent synchronization between the thalamus and the cortex at different oscillation frequencies. The model generally shows how sensory information can be selectively routed depending on its frequency components. |
format | Text |
id | pubmed-2936516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29365162010-09-13 Synaptic Plasticity Controls Sensory Responses through Frequency-Dependent Gamma Oscillation Resonance Paik, Se-Bum Glaser, Donald A. PLoS Comput Biol Research Article Synchronized gamma frequency oscillations in neural networks are thought to be important to sensory information processing, and their effects have been intensively studied. Here we describe a mechanism by which the nervous system can readily control gamma oscillation effects, depending selectively on visual stimuli. Using a model neural network simulation, we found that sensory response in the primary visual cortex is significantly modulated by the resonance between “spontaneous” and “stimulus-driven” oscillations. This gamma resonance can be precisely controlled by the synaptic plasticity of thalamocortical connections, and cortical response is regulated differentially according to the resonance condition. The mechanism produces a selective synchronization between the afferent and downstream neural population. Our simulation results explain experimental observations such as stimulus-dependent synchronization between the thalamus and the cortex at different oscillation frequencies. The model generally shows how sensory information can be selectively routed depending on its frequency components. Public Library of Science 2010-09-09 /pmc/articles/PMC2936516/ /pubmed/20838581 http://dx.doi.org/10.1371/journal.pcbi.1000927 Text en Paik, Glaser. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Paik, Se-Bum Glaser, Donald A. Synaptic Plasticity Controls Sensory Responses through Frequency-Dependent Gamma Oscillation Resonance |
title | Synaptic Plasticity Controls Sensory Responses through Frequency-Dependent Gamma Oscillation Resonance |
title_full | Synaptic Plasticity Controls Sensory Responses through Frequency-Dependent Gamma Oscillation Resonance |
title_fullStr | Synaptic Plasticity Controls Sensory Responses through Frequency-Dependent Gamma Oscillation Resonance |
title_full_unstemmed | Synaptic Plasticity Controls Sensory Responses through Frequency-Dependent Gamma Oscillation Resonance |
title_short | Synaptic Plasticity Controls Sensory Responses through Frequency-Dependent Gamma Oscillation Resonance |
title_sort | synaptic plasticity controls sensory responses through frequency-dependent gamma oscillation resonance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936516/ https://www.ncbi.nlm.nih.gov/pubmed/20838581 http://dx.doi.org/10.1371/journal.pcbi.1000927 |
work_keys_str_mv | AT paiksebum synapticplasticitycontrolssensoryresponsesthroughfrequencydependentgammaoscillationresonance AT glaserdonalda synapticplasticitycontrolssensoryresponsesthroughfrequencydependentgammaoscillationresonance |