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Awakening: Predicting external stimulation to force transitions between different brain states

A fundamental problem in systems neuroscience is how to force a transition from one brain state to another by external driven stimulation in, for example, wakefulness, sleep, coma, or neuropsychiatric diseases. This requires a quantitative and robust definition of a brain state, which has so far pro...

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Autores principales: Deco, Gustavo, Cruzat, Josephine, Cabral, Joana, Tagliazucchi, Enzo, Laufs, Helmut, Logothetis, Nikos K., Kringelbach, Morten L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731634/
https://www.ncbi.nlm.nih.gov/pubmed/31427539
http://dx.doi.org/10.1073/pnas.1905534116
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author Deco, Gustavo
Cruzat, Josephine
Cabral, Joana
Tagliazucchi, Enzo
Laufs, Helmut
Logothetis, Nikos K.
Kringelbach, Morten L.
author_facet Deco, Gustavo
Cruzat, Josephine
Cabral, Joana
Tagliazucchi, Enzo
Laufs, Helmut
Logothetis, Nikos K.
Kringelbach, Morten L.
author_sort Deco, Gustavo
collection PubMed
description A fundamental problem in systems neuroscience is how to force a transition from one brain state to another by external driven stimulation in, for example, wakefulness, sleep, coma, or neuropsychiatric diseases. This requires a quantitative and robust definition of a brain state, which has so far proven elusive. Here, we provide such a definition, which, together with whole-brain modeling, permits the systematic study in silico of how simulated brain stimulation can force transitions between different brain states in humans. Specifically, we use a unique neuroimaging dataset of human sleep to systematically investigate where to stimulate the brain to force an awakening of the human sleeping brain and vice versa. We show where this is possible using a definition of a brain state as an ensemble of “metastable substates,” each with a probabilistic stability and occurrence frequency fitted by a generative whole-brain model, fine-tuned on the basis of the effective connectivity. Given the biophysical limitations of direct electrical stimulation (DES) of microcircuits, this opens exciting possibilities for discovering stimulation targets and selecting connectivity patterns that can ensure propagation of DES-induced neural excitation, potentially making it possible to create awakenings from complex cases of brain injury.
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spelling pubmed-67316342019-09-18 Awakening: Predicting external stimulation to force transitions between different brain states Deco, Gustavo Cruzat, Josephine Cabral, Joana Tagliazucchi, Enzo Laufs, Helmut Logothetis, Nikos K. Kringelbach, Morten L. Proc Natl Acad Sci U S A PNAS Plus A fundamental problem in systems neuroscience is how to force a transition from one brain state to another by external driven stimulation in, for example, wakefulness, sleep, coma, or neuropsychiatric diseases. This requires a quantitative and robust definition of a brain state, which has so far proven elusive. Here, we provide such a definition, which, together with whole-brain modeling, permits the systematic study in silico of how simulated brain stimulation can force transitions between different brain states in humans. Specifically, we use a unique neuroimaging dataset of human sleep to systematically investigate where to stimulate the brain to force an awakening of the human sleeping brain and vice versa. We show where this is possible using a definition of a brain state as an ensemble of “metastable substates,” each with a probabilistic stability and occurrence frequency fitted by a generative whole-brain model, fine-tuned on the basis of the effective connectivity. Given the biophysical limitations of direct electrical stimulation (DES) of microcircuits, this opens exciting possibilities for discovering stimulation targets and selecting connectivity patterns that can ensure propagation of DES-induced neural excitation, potentially making it possible to create awakenings from complex cases of brain injury. National Academy of Sciences 2019-09-03 2019-08-19 /pmc/articles/PMC6731634/ /pubmed/31427539 http://dx.doi.org/10.1073/pnas.1905534116 Text en Copyright © 2019 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle PNAS Plus
Deco, Gustavo
Cruzat, Josephine
Cabral, Joana
Tagliazucchi, Enzo
Laufs, Helmut
Logothetis, Nikos K.
Kringelbach, Morten L.
Awakening: Predicting external stimulation to force transitions between different brain states
title Awakening: Predicting external stimulation to force transitions between different brain states
title_full Awakening: Predicting external stimulation to force transitions between different brain states
title_fullStr Awakening: Predicting external stimulation to force transitions between different brain states
title_full_unstemmed Awakening: Predicting external stimulation to force transitions between different brain states
title_short Awakening: Predicting external stimulation to force transitions between different brain states
title_sort awakening: predicting external stimulation to force transitions between different brain states
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731634/
https://www.ncbi.nlm.nih.gov/pubmed/31427539
http://dx.doi.org/10.1073/pnas.1905534116
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