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Bidirectionally Regulating Gamma Oscillations in Wilson-Cowan Model by Self-Feedback Loops: A Computational Study

The Wilson-Cowan model can emulate gamma oscillations, and thus is extensively used to research the generation of gamma oscillations closely related to cognitive functions. Previous studies have revealed that excitatory and inhibitory inputs to the model can modulate its gamma oscillations. Inhibito...

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Autores principales: Li, XiuPing, Li, ZhengHong, Yang, WanMei, Wu, Zhen, Wang, JunSong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900601/
https://www.ncbi.nlm.nih.gov/pubmed/35264933
http://dx.doi.org/10.3389/fnsys.2022.723237
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author Li, XiuPing
Li, ZhengHong
Yang, WanMei
Wu, Zhen
Wang, JunSong
author_facet Li, XiuPing
Li, ZhengHong
Yang, WanMei
Wu, Zhen
Wang, JunSong
author_sort Li, XiuPing
collection PubMed
description The Wilson-Cowan model can emulate gamma oscillations, and thus is extensively used to research the generation of gamma oscillations closely related to cognitive functions. Previous studies have revealed that excitatory and inhibitory inputs to the model can modulate its gamma oscillations. Inhibitory and excitatory self-feedback loops are important structural features of the model, however, its functional role in the regulation of gamma oscillations in the model is still unclear. In the present study, bifurcation analysis and spectrum analysis are employed to elucidate the regulating mechanism of gamma oscillations underlined by the inhibitory and excitatory self-feedback loops, especially how the two self-feedback loops cooperate to generate the gamma oscillations and regulate the oscillation frequency. The present results reveal that, on one hand, the inhibitory self-feedback loop is not conducive to the generation of gamma oscillations, and increased inhibitory self-feedback strength facilitates the enhancement of the oscillation frequency. On the other hand, the excitatory self-feedback loop promotes the generation of gamma oscillations, and increased excitatory self-feedback strength leads to the decrease of oscillation frequency. Finally, theoretical analysis is conducted to provide explain on how the two self-feedback loops play a crucial role in the generation and regulation of neural oscillations in the model. To sum up, Inhibitory and excitatory self-feedback loops play a complementary role in generating and regulating the gamma oscillation in Wilson-Cowan model, and cooperate to bidirectionally regulate the gamma-oscillation frequency in a more flexible manner. These results might provide testable hypotheses for future experimental research.
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spelling pubmed-89006012022-03-08 Bidirectionally Regulating Gamma Oscillations in Wilson-Cowan Model by Self-Feedback Loops: A Computational Study Li, XiuPing Li, ZhengHong Yang, WanMei Wu, Zhen Wang, JunSong Front Syst Neurosci Neuroscience The Wilson-Cowan model can emulate gamma oscillations, and thus is extensively used to research the generation of gamma oscillations closely related to cognitive functions. Previous studies have revealed that excitatory and inhibitory inputs to the model can modulate its gamma oscillations. Inhibitory and excitatory self-feedback loops are important structural features of the model, however, its functional role in the regulation of gamma oscillations in the model is still unclear. In the present study, bifurcation analysis and spectrum analysis are employed to elucidate the regulating mechanism of gamma oscillations underlined by the inhibitory and excitatory self-feedback loops, especially how the two self-feedback loops cooperate to generate the gamma oscillations and regulate the oscillation frequency. The present results reveal that, on one hand, the inhibitory self-feedback loop is not conducive to the generation of gamma oscillations, and increased inhibitory self-feedback strength facilitates the enhancement of the oscillation frequency. On the other hand, the excitatory self-feedback loop promotes the generation of gamma oscillations, and increased excitatory self-feedback strength leads to the decrease of oscillation frequency. Finally, theoretical analysis is conducted to provide explain on how the two self-feedback loops play a crucial role in the generation and regulation of neural oscillations in the model. To sum up, Inhibitory and excitatory self-feedback loops play a complementary role in generating and regulating the gamma oscillation in Wilson-Cowan model, and cooperate to bidirectionally regulate the gamma-oscillation frequency in a more flexible manner. These results might provide testable hypotheses for future experimental research. Frontiers Media S.A. 2022-02-21 /pmc/articles/PMC8900601/ /pubmed/35264933 http://dx.doi.org/10.3389/fnsys.2022.723237 Text en Copyright © 2022 Li, Li, Yang, Wu and Wang. https://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
Li, XiuPing
Li, ZhengHong
Yang, WanMei
Wu, Zhen
Wang, JunSong
Bidirectionally Regulating Gamma Oscillations in Wilson-Cowan Model by Self-Feedback Loops: A Computational Study
title Bidirectionally Regulating Gamma Oscillations in Wilson-Cowan Model by Self-Feedback Loops: A Computational Study
title_full Bidirectionally Regulating Gamma Oscillations in Wilson-Cowan Model by Self-Feedback Loops: A Computational Study
title_fullStr Bidirectionally Regulating Gamma Oscillations in Wilson-Cowan Model by Self-Feedback Loops: A Computational Study
title_full_unstemmed Bidirectionally Regulating Gamma Oscillations in Wilson-Cowan Model by Self-Feedback Loops: A Computational Study
title_short Bidirectionally Regulating Gamma Oscillations in Wilson-Cowan Model by Self-Feedback Loops: A Computational Study
title_sort bidirectionally regulating gamma oscillations in wilson-cowan model by self-feedback loops: a computational study
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900601/
https://www.ncbi.nlm.nih.gov/pubmed/35264933
http://dx.doi.org/10.3389/fnsys.2022.723237
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