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Enhanced Plasticity of Human Evoked Potentials by Visual Noise During the Intervention of Steady-State Stimulation Based Brain-Computer Interface

Neuroplasticity, also known as brain plasticity, is an inclusive term that covers the permanent changes in the brain during the course of an individual's life, and neuroplasticity can be broadly defined as the changes in function or structure of the brain in response to the external and/or inte...

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Autores principales: Xie, Jun, Xu, Guanghua, Zhao, Xingang, Li, Min, Wang, Jing, Han, Chengcheng, Han, Xingliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282004/
https://www.ncbi.nlm.nih.gov/pubmed/30555316
http://dx.doi.org/10.3389/fnbot.2018.00082
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author Xie, Jun
Xu, Guanghua
Zhao, Xingang
Li, Min
Wang, Jing
Han, Chengcheng
Han, Xingliang
author_facet Xie, Jun
Xu, Guanghua
Zhao, Xingang
Li, Min
Wang, Jing
Han, Chengcheng
Han, Xingliang
author_sort Xie, Jun
collection PubMed
description Neuroplasticity, also known as brain plasticity, is an inclusive term that covers the permanent changes in the brain during the course of an individual's life, and neuroplasticity can be broadly defined as the changes in function or structure of the brain in response to the external and/or internal influences. Long-term potentiation (LTP), a well-characterized form of functional synaptic plasticity, could be influenced by rapid-frequency stimulation (or “tetanus”) within in vivo human sensory pathways. Also, stochastic resonance (SR) has brought new insight into the field of visual processing for the study of neuroplasticity. In the present study, a brain-computer interface (BCI) intervention based on rapid and repetitive motion-reversal visual stimulation (i.e., a “tetanizing” stimulation) associated with spatiotemporal visual noise was implemented. The goal was to explore the possibility that the induction of LTP-like plasticity in the visual cortex may be enhanced by the SR formalism via changes in the amplitude of visual evoked potentials (VEPs) measured non-invasively from the scalp of healthy subjects. Changes in the absolute amplitude of P1 and N1 components of the transient VEPs during the initial presentation of the steady-state stimulation were used to evaluate the LTP-like plasticity between the non-noise and noise-tagged BCI interventions. We have shown that after adding a moderate visual noise to the rapid-frequency visual stimulation, the degree of the N1 negativity was potentiated following an ~40-min noise-tagged visual tetani. This finding demonstrated that the SR mechanism could enhance the plasticity-like changes in the human visual cortex.
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spelling pubmed-62820042018-12-14 Enhanced Plasticity of Human Evoked Potentials by Visual Noise During the Intervention of Steady-State Stimulation Based Brain-Computer Interface Xie, Jun Xu, Guanghua Zhao, Xingang Li, Min Wang, Jing Han, Chengcheng Han, Xingliang Front Neurorobot Neuroscience Neuroplasticity, also known as brain plasticity, is an inclusive term that covers the permanent changes in the brain during the course of an individual's life, and neuroplasticity can be broadly defined as the changes in function or structure of the brain in response to the external and/or internal influences. Long-term potentiation (LTP), a well-characterized form of functional synaptic plasticity, could be influenced by rapid-frequency stimulation (or “tetanus”) within in vivo human sensory pathways. Also, stochastic resonance (SR) has brought new insight into the field of visual processing for the study of neuroplasticity. In the present study, a brain-computer interface (BCI) intervention based on rapid and repetitive motion-reversal visual stimulation (i.e., a “tetanizing” stimulation) associated with spatiotemporal visual noise was implemented. The goal was to explore the possibility that the induction of LTP-like plasticity in the visual cortex may be enhanced by the SR formalism via changes in the amplitude of visual evoked potentials (VEPs) measured non-invasively from the scalp of healthy subjects. Changes in the absolute amplitude of P1 and N1 components of the transient VEPs during the initial presentation of the steady-state stimulation were used to evaluate the LTP-like plasticity between the non-noise and noise-tagged BCI interventions. We have shown that after adding a moderate visual noise to the rapid-frequency visual stimulation, the degree of the N1 negativity was potentiated following an ~40-min noise-tagged visual tetani. This finding demonstrated that the SR mechanism could enhance the plasticity-like changes in the human visual cortex. Frontiers Media S.A. 2018-11-29 /pmc/articles/PMC6282004/ /pubmed/30555316 http://dx.doi.org/10.3389/fnbot.2018.00082 Text en Copyright © 2018 Xie, Xu, Zhao, Li, Wang, Han and Han. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Xie, Jun
Xu, Guanghua
Zhao, Xingang
Li, Min
Wang, Jing
Han, Chengcheng
Han, Xingliang
Enhanced Plasticity of Human Evoked Potentials by Visual Noise During the Intervention of Steady-State Stimulation Based Brain-Computer Interface
title Enhanced Plasticity of Human Evoked Potentials by Visual Noise During the Intervention of Steady-State Stimulation Based Brain-Computer Interface
title_full Enhanced Plasticity of Human Evoked Potentials by Visual Noise During the Intervention of Steady-State Stimulation Based Brain-Computer Interface
title_fullStr Enhanced Plasticity of Human Evoked Potentials by Visual Noise During the Intervention of Steady-State Stimulation Based Brain-Computer Interface
title_full_unstemmed Enhanced Plasticity of Human Evoked Potentials by Visual Noise During the Intervention of Steady-State Stimulation Based Brain-Computer Interface
title_short Enhanced Plasticity of Human Evoked Potentials by Visual Noise During the Intervention of Steady-State Stimulation Based Brain-Computer Interface
title_sort enhanced plasticity of human evoked potentials by visual noise during the intervention of steady-state stimulation based brain-computer interface
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282004/
https://www.ncbi.nlm.nih.gov/pubmed/30555316
http://dx.doi.org/10.3389/fnbot.2018.00082
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