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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...

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Autores principales: Blanpain, Lou T., Chen, Emily., Park, James, Walelign, Michael Y., Gross, Robert E., Cabaniss, Brian T., Willie, Jon T., Singer, Annabelle C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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.
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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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