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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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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 |
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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 |
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