Cargando…

Medial temporal lobe functional connectivity predicts stimulation-induced theta power

Focal electrical stimulation of the brain incites a cascade of neural activity that propagates from the stimulated region to both nearby and remote areas, offering the potential to control the activity of brain networks. Understanding how exogenous electrical signals perturb such networks in humans...

Descripción completa

Detalles Bibliográficos
Autores principales: Solomon, E. A., Kragel, J. E., Gross, R., Lega, B., Sperling, M. R., Worrell, G., Sheth, S. A., Zaghloul, K. A., Jobst, B. C., Stein, J. M., Das, S., Gorniak, R., Inman, C. S., Seger, S., Rizzuto, D. S., Kahana, M. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202342/
https://www.ncbi.nlm.nih.gov/pubmed/30361627
http://dx.doi.org/10.1038/s41467-018-06876-w
_version_ 1783365657496125440
author Solomon, E. A.
Kragel, J. E.
Gross, R.
Lega, B.
Sperling, M. R.
Worrell, G.
Sheth, S. A.
Zaghloul, K. A.
Jobst, B. C.
Stein, J. M.
Das, S.
Gorniak, R.
Inman, C. S.
Seger, S.
Rizzuto, D. S.
Kahana, M. J.
author_facet Solomon, E. A.
Kragel, J. E.
Gross, R.
Lega, B.
Sperling, M. R.
Worrell, G.
Sheth, S. A.
Zaghloul, K. A.
Jobst, B. C.
Stein, J. M.
Das, S.
Gorniak, R.
Inman, C. S.
Seger, S.
Rizzuto, D. S.
Kahana, M. J.
author_sort Solomon, E. A.
collection PubMed
description Focal electrical stimulation of the brain incites a cascade of neural activity that propagates from the stimulated region to both nearby and remote areas, offering the potential to control the activity of brain networks. Understanding how exogenous electrical signals perturb such networks in humans is key to its clinical translation. To investigate this, we applied electrical stimulation to subregions of the medial temporal lobe in 26 neurosurgical patients fitted with indwelling electrodes. Networks of low-frequency (5–13 Hz) spectral coherence predicted stimulation-evoked increases in theta (5–8 Hz) power, particularly when stimulation was applied in or adjacent to white matter. Stimulation tended to decrease power in the high-frequency broadband (HFB; 50–200 Hz) range, and these modulations were correlated with HFB-based networks in a subset of subjects. Our results demonstrate that functional connectivity is predictive of causal changes in the brain, capturing evoked activity across brain regions and frequency bands.
format Online
Article
Text
id pubmed-6202342
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-62023422018-10-29 Medial temporal lobe functional connectivity predicts stimulation-induced theta power Solomon, E. A. Kragel, J. E. Gross, R. Lega, B. Sperling, M. R. Worrell, G. Sheth, S. A. Zaghloul, K. A. Jobst, B. C. Stein, J. M. Das, S. Gorniak, R. Inman, C. S. Seger, S. Rizzuto, D. S. Kahana, M. J. Nat Commun Article Focal electrical stimulation of the brain incites a cascade of neural activity that propagates from the stimulated region to both nearby and remote areas, offering the potential to control the activity of brain networks. Understanding how exogenous electrical signals perturb such networks in humans is key to its clinical translation. To investigate this, we applied electrical stimulation to subregions of the medial temporal lobe in 26 neurosurgical patients fitted with indwelling electrodes. Networks of low-frequency (5–13 Hz) spectral coherence predicted stimulation-evoked increases in theta (5–8 Hz) power, particularly when stimulation was applied in or adjacent to white matter. Stimulation tended to decrease power in the high-frequency broadband (HFB; 50–200 Hz) range, and these modulations were correlated with HFB-based networks in a subset of subjects. Our results demonstrate that functional connectivity is predictive of causal changes in the brain, capturing evoked activity across brain regions and frequency bands. Nature Publishing Group UK 2018-10-25 /pmc/articles/PMC6202342/ /pubmed/30361627 http://dx.doi.org/10.1038/s41467-018-06876-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Solomon, E. A.
Kragel, J. E.
Gross, R.
Lega, B.
Sperling, M. R.
Worrell, G.
Sheth, S. A.
Zaghloul, K. A.
Jobst, B. C.
Stein, J. M.
Das, S.
Gorniak, R.
Inman, C. S.
Seger, S.
Rizzuto, D. S.
Kahana, M. J.
Medial temporal lobe functional connectivity predicts stimulation-induced theta power
title Medial temporal lobe functional connectivity predicts stimulation-induced theta power
title_full Medial temporal lobe functional connectivity predicts stimulation-induced theta power
title_fullStr Medial temporal lobe functional connectivity predicts stimulation-induced theta power
title_full_unstemmed Medial temporal lobe functional connectivity predicts stimulation-induced theta power
title_short Medial temporal lobe functional connectivity predicts stimulation-induced theta power
title_sort medial temporal lobe functional connectivity predicts stimulation-induced theta power
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202342/
https://www.ncbi.nlm.nih.gov/pubmed/30361627
http://dx.doi.org/10.1038/s41467-018-06876-w
work_keys_str_mv AT solomonea medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT kragelje medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT grossr medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT legab medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT sperlingmr medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT worrellg medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT shethsa medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT zaghloulka medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT jobstbc medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT steinjm medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT dass medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT gorniakr medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT inmancs medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT segers medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT rizzutods medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower
AT kahanamj medialtemporallobefunctionalconnectivitypredictsstimulationinducedthetapower