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Multisensory Flicker Modulates Widespread Brain Networks and Reduces Interictal Epileptiform Discharges in Humans
Modulating brain oscillations has strong therapeutic potential. However, commonly used non-invasive interventions such as transcranial magnetic or direct current stimulation have limited effects on deeper cortical structures like the medial temporal lobe. Repetitive audio-visual stimulation, or sens...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055448/ https://www.ncbi.nlm.nih.gov/pubmed/36993248 http://dx.doi.org/10.1101/2023.03.14.23286691 |
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author | Blanpain, Lou T. Chen, Emily. Park, James Walelign, Michael Y. Gross, Robert E. Cabaniss, Brian T. Willie, Jon T. Singer, Annabelle C. |
author_facet | Blanpain, Lou T. Chen, Emily. Park, James Walelign, Michael Y. Gross, Robert E. Cabaniss, Brian T. Willie, Jon T. Singer, Annabelle C. |
author_sort | Blanpain, Lou T. |
collection | PubMed |
description | Modulating brain oscillations has strong therapeutic potential. However, commonly used non-invasive interventions such as transcranial magnetic or direct current stimulation have limited effects on deeper cortical structures like the medial temporal lobe. Repetitive audio-visual stimulation, or sensory flicker, modulates such structures in mice but little is known about its effects in humans. Using high spatiotemporal resolution, we mapped and quantified the neurophysiological effects of sensory flicker in human subjects undergoing presurgical intracranial seizure monitoring. We found that flicker modulates both local field potential and single neurons in higher cognitive regions, including the medial temporal lobe and prefrontal cortex, and that local field potential modulation is likely mediated via resonance of involved circuits. We then assessed how flicker affects pathological neural activity, specifically interictal epileptiform discharges, a biomarker of epilepsy also implicated in Alzheimer’s and other diseases. In our patient population with focal seizure onsets, sensory flicker decreased the rate interictal epileptiform discharges. Our findings support the use of sensory flicker to modulate deeper cortical structures and mitigate pathological activity in humans. |
format | Online Article Text |
id | pubmed-10055448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100554482023-03-30 Multisensory Flicker Modulates Widespread Brain Networks and Reduces Interictal Epileptiform Discharges in Humans Blanpain, Lou T. Chen, Emily. Park, James Walelign, Michael Y. Gross, Robert E. Cabaniss, Brian T. Willie, Jon T. Singer, Annabelle C. medRxiv Article Modulating brain oscillations has strong therapeutic potential. However, commonly used non-invasive interventions such as transcranial magnetic or direct current stimulation have limited effects on deeper cortical structures like the medial temporal lobe. Repetitive audio-visual stimulation, or sensory flicker, modulates such structures in mice but little is known about its effects in humans. Using high spatiotemporal resolution, we mapped and quantified the neurophysiological effects of sensory flicker in human subjects undergoing presurgical intracranial seizure monitoring. We found that flicker modulates both local field potential and single neurons in higher cognitive regions, including the medial temporal lobe and prefrontal cortex, and that local field potential modulation is likely mediated via resonance of involved circuits. We then assessed how flicker affects pathological neural activity, specifically interictal epileptiform discharges, a biomarker of epilepsy also implicated in Alzheimer’s and other diseases. In our patient population with focal seizure onsets, sensory flicker decreased the rate interictal epileptiform discharges. Our findings support the use of sensory flicker to modulate deeper cortical structures and mitigate pathological activity in humans. Cold Spring Harbor Laboratory 2023-03-17 /pmc/articles/PMC10055448/ /pubmed/36993248 http://dx.doi.org/10.1101/2023.03.14.23286691 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Blanpain, Lou T. Chen, Emily. Park, James Walelign, Michael Y. Gross, Robert E. Cabaniss, Brian T. Willie, Jon T. Singer, Annabelle C. Multisensory Flicker Modulates Widespread Brain Networks and Reduces Interictal Epileptiform Discharges in Humans |
title | Multisensory Flicker Modulates Widespread Brain Networks and Reduces Interictal Epileptiform Discharges in Humans |
title_full | Multisensory Flicker Modulates Widespread Brain Networks and Reduces Interictal Epileptiform Discharges in Humans |
title_fullStr | Multisensory Flicker Modulates Widespread Brain Networks and Reduces Interictal Epileptiform Discharges in Humans |
title_full_unstemmed | Multisensory Flicker Modulates Widespread Brain Networks and Reduces Interictal Epileptiform Discharges in Humans |
title_short | Multisensory Flicker Modulates Widespread Brain Networks and Reduces Interictal Epileptiform Discharges in Humans |
title_sort | multisensory flicker modulates widespread brain networks and reduces interictal epileptiform discharges in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055448/ https://www.ncbi.nlm.nih.gov/pubmed/36993248 http://dx.doi.org/10.1101/2023.03.14.23286691 |
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