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Suppression of Low-Frequency Gamma Oscillations by Activation of 40-Hz Oscillation

Gamma oscillations have received considerable attention owing to their association with cognitive function and various neuropsychiatric disorders. However, interactions of gamma oscillations at different frequency bands in humans remain unclear. In the present magnetoencephalographic study, brain os...

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Autores principales: Sugiyama, Shunsuke, Taniguchi, Tomoya, Kinukawa, Tomoaki, Takeuchi, Nobuyuki, Ohi, Kazutaka, Shioiri, Toshiki, Nishihara, Makoto, Inui, Koji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9247420/
https://www.ncbi.nlm.nih.gov/pubmed/34689202
http://dx.doi.org/10.1093/cercor/bhab381
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author Sugiyama, Shunsuke
Taniguchi, Tomoya
Kinukawa, Tomoaki
Takeuchi, Nobuyuki
Ohi, Kazutaka
Shioiri, Toshiki
Nishihara, Makoto
Inui, Koji
author_facet Sugiyama, Shunsuke
Taniguchi, Tomoya
Kinukawa, Tomoaki
Takeuchi, Nobuyuki
Ohi, Kazutaka
Shioiri, Toshiki
Nishihara, Makoto
Inui, Koji
author_sort Sugiyama, Shunsuke
collection PubMed
description Gamma oscillations have received considerable attention owing to their association with cognitive function and various neuropsychiatric disorders. However, interactions of gamma oscillations at different frequency bands in humans remain unclear. In the present magnetoencephalographic study, brain oscillations in a wide frequency range were examined using a time-frequency analysis during the 20-, 30-, 40-, and 50-Hz auditory stimuli in 21 healthy subjects. First, dipoles for auditory steady-state response (ASSR) were estimated and interaction among oscillations at 10–60 Hz was examined using the source strength waveforms. Results showed the suppression of ongoing low-gamma oscillations at approximately 30 Hz during stimulation at 40 Hz. Second, multi-dipole analyses suggested that the main dipole for ASSR and dipoles for suppressed low-frequency gamma oscillations were distinct. Third, an all-sensor analysis was performed to clarify the distribution of the 40-Hz ASSR and suppression of low-frequency gamma oscillations. Notably, the area of suppression surrounded the center of the 40-Hz ASSR and showed a trend of extending to the vertex, indicating that different groups of neurons were responsible for these two gamma oscillations and that the 40-Hz oscillation circuit have specific inhibitory innervation to the low-gamma circuit.
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spelling pubmed-92474202022-07-05 Suppression of Low-Frequency Gamma Oscillations by Activation of 40-Hz Oscillation Sugiyama, Shunsuke Taniguchi, Tomoya Kinukawa, Tomoaki Takeuchi, Nobuyuki Ohi, Kazutaka Shioiri, Toshiki Nishihara, Makoto Inui, Koji Cereb Cortex Original Article Gamma oscillations have received considerable attention owing to their association with cognitive function and various neuropsychiatric disorders. However, interactions of gamma oscillations at different frequency bands in humans remain unclear. In the present magnetoencephalographic study, brain oscillations in a wide frequency range were examined using a time-frequency analysis during the 20-, 30-, 40-, and 50-Hz auditory stimuli in 21 healthy subjects. First, dipoles for auditory steady-state response (ASSR) were estimated and interaction among oscillations at 10–60 Hz was examined using the source strength waveforms. Results showed the suppression of ongoing low-gamma oscillations at approximately 30 Hz during stimulation at 40 Hz. Second, multi-dipole analyses suggested that the main dipole for ASSR and dipoles for suppressed low-frequency gamma oscillations were distinct. Third, an all-sensor analysis was performed to clarify the distribution of the 40-Hz ASSR and suppression of low-frequency gamma oscillations. Notably, the area of suppression surrounded the center of the 40-Hz ASSR and showed a trend of extending to the vertex, indicating that different groups of neurons were responsible for these two gamma oscillations and that the 40-Hz oscillation circuit have specific inhibitory innervation to the low-gamma circuit. Oxford University Press 2021-10-23 /pmc/articles/PMC9247420/ /pubmed/34689202 http://dx.doi.org/10.1093/cercor/bhab381 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sugiyama, Shunsuke
Taniguchi, Tomoya
Kinukawa, Tomoaki
Takeuchi, Nobuyuki
Ohi, Kazutaka
Shioiri, Toshiki
Nishihara, Makoto
Inui, Koji
Suppression of Low-Frequency Gamma Oscillations by Activation of 40-Hz Oscillation
title Suppression of Low-Frequency Gamma Oscillations by Activation of 40-Hz Oscillation
title_full Suppression of Low-Frequency Gamma Oscillations by Activation of 40-Hz Oscillation
title_fullStr Suppression of Low-Frequency Gamma Oscillations by Activation of 40-Hz Oscillation
title_full_unstemmed Suppression of Low-Frequency Gamma Oscillations by Activation of 40-Hz Oscillation
title_short Suppression of Low-Frequency Gamma Oscillations by Activation of 40-Hz Oscillation
title_sort suppression of low-frequency gamma oscillations by activation of 40-hz oscillation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9247420/
https://www.ncbi.nlm.nih.gov/pubmed/34689202
http://dx.doi.org/10.1093/cercor/bhab381
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