High-order brain interactions in ketamine during rest and task: a double-blinded cross-over design using portable EEG on male participants.


Journal

Translational psychiatry
ISSN: 2158-3188
Titre abrégé: Transl Psychiatry
Pays: United States
ID NLM: 101562664

Informations de publication

Date de publication:
27 Jul 2024
Historique:
received: 13 02 2024
accepted: 17 07 2024
revised: 12 07 2024
medline: 28 7 2024
pubmed: 28 7 2024
entrez: 27 7 2024
Statut: epublish

Résumé

Ketamine is a dissociative anesthetic that induces a shift in global consciousness states and related brain dynamics. Portable low-density EEG systems could be used to monitor these effects. However, previous evidence is almost null and lacks adequate methods to address global dynamics with a small number of electrodes. This study delves into brain high-order interactions (HOI) to explore the effects of ketamine using portable EEG. In a double-blinded cross-over design, 30 male adults (mean age = 25.57, SD = 3.74) were administered racemic ketamine and compared against saline infusion as a control. Both task-driven (auditory oddball paradigm) and resting-state EEG were recorded. HOI were computed using advanced multivariate information theory tools, allowing us to quantify nonlinear statistical dependencies between all possible electrode combinations. Ketamine induced an increase in redundancy in brain dynamics (copies of the same information that can be retrieved from 3 or more electrodes), most significantly in the alpha frequency band. Redundancy was more evident during resting state, associated with a shift in conscious states towards more dissociative tendencies. Furthermore, in the task-driven context (auditory oddball), the impact of ketamine on redundancy was more significant for predictable (standard stimuli) compared to deviant ones. Finally, associations were observed between ketamine's HOI and experiences of derealization. Ketamine appears to increase redundancy and HOI across psychometric measures, suggesting these effects are correlated with alterations in consciousness towards dissociation. In comparisons with event-related potential (ERP) or standard functional connectivity metrics, HOI represent an innovative method to combine all signal spatial interactions obtained from low-density dry EEG in drug interventions, as it is the only approach that exploits all possible combinations between electrodes. This research emphasizes the potential of complexity measures coupled with portable EEG devices in monitoring shifts in consciousness, especially when paired with low-density configurations, paving the way for better understanding and monitoring of pharmacological-induced changes.

Identifiants

pubmed: 39068157
doi: 10.1038/s41398-024-03029-0
pii: 10.1038/s41398-024-03029-0
doi:

Substances chimiques

Ketamine 690G0D6V8H
Anesthetics, Dissociative 0

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

310

Informations de copyright

© 2024. The Author(s).

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Auteurs

Rubén Herzog (R)

Latin American Brain Health Institute, Universidad Adolfo Ibañez, Santiago de Chile, Chile. ruben.herzog@icm-institute.org.
Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, Paris, France. ruben.herzog@icm-institute.org.

Florentine Marie Barbey (FM)

Cumulus Neuroscience Ltd, Dublin, Ireland.

Md Nurul Islam (MN)

Cumulus Neuroscience Ltd, Dublin, Ireland.

Laura Rueda-Delgado (L)

Cumulus Neuroscience Ltd, Dublin, Ireland.

Hugh Nolan (H)

Cumulus Neuroscience Ltd, Dublin, Ireland.

Pavel Prado (P)

Escuela de Fonoaudiología, Facultad de Odontología y Ciencias de la Rehabilitación, Universidad San Sebastián, Santiago, Chile.

Marina Krylova (M)

Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany.

Igor Izyurov (I)

Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany.

Nooshin Javaheripour (N)

Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany.

Lena Vera Danyeli (LV)

Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany.

Zümrüt Duygu Sen (ZD)

Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany.

Martin Walter (M)

Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany.
German Center for Mental Health (DZPG), partner site Halle-Jena-Magdeburg, Jena, Germany.

Patricio O'Donnell (P)

Neuroscience Drug Discovery Unit, Takeda Pharmaceuticals, Cambridge, MA, 02390, USA.

Derek L Buhl (DL)

Neuroscience Drug Discovery Unit, Takeda Pharmaceuticals, Cambridge, MA, 02390, USA.

Brian Murphy (B)

Cumulus Neuroscience Ltd, Dublin, Ireland.

Agustin Ibanez (A)

Latin American Brain Health Institute, Universidad Adolfo Ibañez, Santiago de Chile, Chile. agustin.ibanez@gbhi.org.
Global Brain Health Institute, UCSF and Trinity College Dublin, Dublin, Ireland. agustin.ibanez@gbhi.org.

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