Cargando…

Theta-burst stimulation entrains frequency-specific oscillatory responses

BACKGROUND: Brain stimulation has emerged as a powerful tool in human neuroscience, becoming integral to next-generation psychiatric and neurologic therapeutics. Theta-burst stimulation (TBS), in which electrical pulses are delivered in rhythmic bouts of 3–8 Hz, seeks to recapitulate neural activity...

Descripción completa

Detalles Bibliográficos
Autores principales: Solomon, Ethan A., Sperling, Michael R., Sharan, Ashwini D., Wanda, Paul A., Levy, Deborah F., Lyalenko, Anastasia, Pedisich, Isaac, Rizzuto, Daniel S., Kahana, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161680/
https://www.ncbi.nlm.nih.gov/pubmed/34428553
http://dx.doi.org/10.1016/j.brs.2021.08.014
_version_ 1784719536557129728
author Solomon, Ethan A.
Sperling, Michael R.
Sharan, Ashwini D.
Wanda, Paul A.
Levy, Deborah F.
Lyalenko, Anastasia
Pedisich, Isaac
Rizzuto, Daniel S.
Kahana, Michael J.
author_facet Solomon, Ethan A.
Sperling, Michael R.
Sharan, Ashwini D.
Wanda, Paul A.
Levy, Deborah F.
Lyalenko, Anastasia
Pedisich, Isaac
Rizzuto, Daniel S.
Kahana, Michael J.
author_sort Solomon, Ethan A.
collection PubMed
description BACKGROUND: Brain stimulation has emerged as a powerful tool in human neuroscience, becoming integral to next-generation psychiatric and neurologic therapeutics. Theta-burst stimulation (TBS), in which electrical pulses are delivered in rhythmic bouts of 3–8 Hz, seeks to recapitulate neural activity seen endogenously during cognitive tasks. A growing literature suggests that TBS can be used to alter or enhance cognitive processes, but little is known about how these stimulation events influence underlying neural activity. OBJECTIVE: Our study sought to investigate the effect of direct electrical TBS on mesoscale neural activity in humans by asking (1) whether TBS evokes persistent theta oscillations in cortical areas, (2) whether these oscillations occur at the stimulated frequency, and (3) whether stimulation events propagate in a manner consistent with underlying functional and structural brain architecture. METHODS: We recruited 20 neurosurgical epilepsy patients with indwelling electrodes and delivered direct cortical TBS at varying locations and frequencies. Simultaneous iEEG was recorded from non-stimulated electrodes and analyzed to understand how TBS influences mesoscale neural activity. RESULTS: We found that TBS rapidly evoked theta rhythms in widespread brain regions, preferentially at the stimulation frequency, and that these oscillations persisted for hundreds of milliseconds post stimulation offset. Furthermore, the functional connectivity between recording and stimulation sites predicted the strength of theta response, suggesting that underlying brain architecture guides the flow of stimulation through the brain. CONCLUSIONS: By demonstrating that cortical TBS induces frequency-specific oscillatory responses, our results suggest this technology can be used to directly and predictably influence the activity of cognitively-relevant brain networks.
format Online
Article
Text
id pubmed-9161680
institution National Center for Biotechnology Information
language English
publishDate 2021
record_format MEDLINE/PubMed
spelling pubmed-91616802022-06-02 Theta-burst stimulation entrains frequency-specific oscillatory responses Solomon, Ethan A. Sperling, Michael R. Sharan, Ashwini D. Wanda, Paul A. Levy, Deborah F. Lyalenko, Anastasia Pedisich, Isaac Rizzuto, Daniel S. Kahana, Michael J. Brain Stimul Article BACKGROUND: Brain stimulation has emerged as a powerful tool in human neuroscience, becoming integral to next-generation psychiatric and neurologic therapeutics. Theta-burst stimulation (TBS), in which electrical pulses are delivered in rhythmic bouts of 3–8 Hz, seeks to recapitulate neural activity seen endogenously during cognitive tasks. A growing literature suggests that TBS can be used to alter or enhance cognitive processes, but little is known about how these stimulation events influence underlying neural activity. OBJECTIVE: Our study sought to investigate the effect of direct electrical TBS on mesoscale neural activity in humans by asking (1) whether TBS evokes persistent theta oscillations in cortical areas, (2) whether these oscillations occur at the stimulated frequency, and (3) whether stimulation events propagate in a manner consistent with underlying functional and structural brain architecture. METHODS: We recruited 20 neurosurgical epilepsy patients with indwelling electrodes and delivered direct cortical TBS at varying locations and frequencies. Simultaneous iEEG was recorded from non-stimulated electrodes and analyzed to understand how TBS influences mesoscale neural activity. RESULTS: We found that TBS rapidly evoked theta rhythms in widespread brain regions, preferentially at the stimulation frequency, and that these oscillations persisted for hundreds of milliseconds post stimulation offset. Furthermore, the functional connectivity between recording and stimulation sites predicted the strength of theta response, suggesting that underlying brain architecture guides the flow of stimulation through the brain. CONCLUSIONS: By demonstrating that cortical TBS induces frequency-specific oscillatory responses, our results suggest this technology can be used to directly and predictably influence the activity of cognitively-relevant brain networks. 2021 2021-08-21 /pmc/articles/PMC9161680/ /pubmed/34428553 http://dx.doi.org/10.1016/j.brs.2021.08.014 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Solomon, Ethan A.
Sperling, Michael R.
Sharan, Ashwini D.
Wanda, Paul A.
Levy, Deborah F.
Lyalenko, Anastasia
Pedisich, Isaac
Rizzuto, Daniel S.
Kahana, Michael J.
Theta-burst stimulation entrains frequency-specific oscillatory responses
title Theta-burst stimulation entrains frequency-specific oscillatory responses
title_full Theta-burst stimulation entrains frequency-specific oscillatory responses
title_fullStr Theta-burst stimulation entrains frequency-specific oscillatory responses
title_full_unstemmed Theta-burst stimulation entrains frequency-specific oscillatory responses
title_short Theta-burst stimulation entrains frequency-specific oscillatory responses
title_sort theta-burst stimulation entrains frequency-specific oscillatory responses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161680/
https://www.ncbi.nlm.nih.gov/pubmed/34428553
http://dx.doi.org/10.1016/j.brs.2021.08.014
work_keys_str_mv AT solomonethana thetaburststimulationentrainsfrequencyspecificoscillatoryresponses
AT sperlingmichaelr thetaburststimulationentrainsfrequencyspecificoscillatoryresponses
AT sharanashwinid thetaburststimulationentrainsfrequencyspecificoscillatoryresponses
AT wandapaula thetaburststimulationentrainsfrequencyspecificoscillatoryresponses
AT levydeborahf thetaburststimulationentrainsfrequencyspecificoscillatoryresponses
AT lyalenkoanastasia thetaburststimulationentrainsfrequencyspecificoscillatoryresponses
AT pedisichisaac thetaburststimulationentrainsfrequencyspecificoscillatoryresponses
AT rizzutodaniels thetaburststimulationentrainsfrequencyspecificoscillatoryresponses
AT kahanamichaelj thetaburststimulationentrainsfrequencyspecificoscillatoryresponses