Psilocybin-induced EEG spectral changes of functional networks in healthy subjects.

Poster No:

1353 

Submission Type:

Late-Breaking Abstract Submission 

Authors:

Vidushani Dhanawansa1, Devon Stoliker2, Leonardo Novelli2, Mana Biabani1, Adeel Razi1, Levin Kuhlmann2

Institutions:

1Monash University, Melbourne, VIC, 2Monash University, Melbourne, Victoria

First Author:

Vidushani Dhanawansa  
Monash University
Melbourne, VIC

Co-Author(s):

Devon Stoliker, PhD  
Monash University
Melbourne, Victoria
Leonardo Novelli  
Monash University
Melbourne, Victoria
Mana Biabani  
Monash University
Melbourne, VIC
Adeel Razi  
Monash University
Melbourne, VIC
Levin Kuhlmann  
Monash University
Melbourne, Victoria

Late Breaking Reviewer(s):

Jean Chen  
Rotman Research Institute, Baycrest
Toronto, Ontario
Marta Garrido  
The University of Melbourne
Melbourne, Australia
Nicola Palomero-Gallagher  
Research Centre Jülich
Jülich, Jülich

Introduction:

Psilocybin, a serotonergic psychedelic, is valuable in studying altered states of consciousness and has shown efficacy in alleviating depressive symptoms(Haikazian et al., 2023). Since brain region inhibition and engagement are mediated by different frequency bands(Jensen & Mazaheri, 2010), studying psilocybin-induced broadband neural changes via EEG imaging could improve understanding of its subjective effects. Also, exploring functional connectivity (FC) between functionally relevant cortical regions rather than anatomical divisions could offer new insights(Kometer et al., 2015; Pallavicini et al., 2019). Major depressive disorder (MDD) patients exhibit higher alpha and beta coherence, but psilocybin's modulation of this remains unclear. To address this gap, we computed frequency specific resting-state FC using source-reconstructed EEG on the current largest non-clinical psychedelic imaging dataset.

Methods:

Eyes-closed resting-state EEG scans of baseline and post-administration(19mg psilocybin) were acquired from 56 participants using a 64-electrode cap. EEG preprocessing was followed by Minimum Norm Estimation (MNE) based EEG source reconstruction(Baillet et al., 2001). Electrode positions were co-registered with head anatomies, and Boundary Element Models (BEM) were generated. Source estimation resulted in 15002 electric dipoles constrained normal to the cortical surface. The Welch periodogram was computed with Hanning tapers on 2s epochs with 50% overlap. Source power maps generated within six canonical frequency bands were projected to the default anatomical surface and smoothened. Paired t-tests between baseline and psilocybin sessions analyzed group effects.
Resting-state functional connectivity (RSFC) was inferred via magnitude-squared coherence (MSC) within Yeo17 atlas networks using 100 Schaefer cortical parcellations. MSC was computed between principal components of each region, and time-frequency decomposition was achieved via Hilbert transform. Paired tests assessed the differences of the mean within-network MSC of all networks and frequency bands between sessions. All tests applied 5000 permutations and FDR correction at 0.05.

Results:

Psilocybin increased frontal delta power and decreased occipital delta power, induced widespread theta power decreases, reduced alpha power in DMN and visual networks, and increased gamma power(Fig.1). DMN-A (core DMN) engaged in self-referential processing, and DMN-B linked to planning showed FC decreases in the alpha and beta bands, but did not survive multiple comparison correction. FC decreased in the salience networks in the same bands. Psilocybin significantly increased FC in central and peripheral visual networks across all frequency bands except alpha(Fig.2).
Supporting Image: OHBM_3672_Fig1.jpg
Supporting Image: OHBM_3672_Fig2.jpg
 

Conclusions:

The DMN, integral to self-referential thought, exhibits hyperconnectivity in MDD(Broyd et al., 2009), highlighting its importance in interventions. MDD patients show higher alpha and beta coherence, critical for top-down control(Klimesch et al., 2007) and this increased alpha coherence may reflect impaired top-down regulation. Our findings show psilocybin acutely decreases RSFC in DMN, salience, and somatomotor networks in alpha and beta bands, key in top-down control. While studied in healthy subjects, psilocybin could modulate MDD-related coherence abnormalities, particularly in lower frequencies, normalizing dysfunctional top-down regulation.
Conversely, we found increased gamma FC, associated with neuronal excitation. This decrease in alpha and increase in gamma power supports the idea of a psilocybin-induced shift in excitation/inhibition balance toward excitation, contributing to altered states of consciousness. Additionally, increased visual network FC in non-alpha bands suggests a loss of alpha dominance, possibly linked to psychedelic-induced visual effects.
We contribute to the understanding how psilocybin could modulate neural markers of depression, such as dysfunctional DMN hyperconnectivity and impaired top-down control.

Higher Cognitive Functions:

Executive Function, Cognitive Control and Decision Making

Modeling and Analysis Methods:

Connectivity (eg. functional, effective, structural)
EEG/MEG Modeling and Analysis 1
Task-Independent and Resting-State Analysis 2

Keywords:

Electroencephaolography (EEG)
Other - Resting state functional connectivity; Psilocybin; Default Mode Network

1|2Indicates the priority used for review

Abstract Information

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Please indicate below if your study was a "resting state" or "task-activation” study.

Resting state

Healthy subjects only or patients (note that patient studies may also involve healthy subjects):

Healthy subjects

Was this research conducted in the United States?

No

Were any human subjects research approved by the relevant Institutional Review Board or ethics panel? NOTE: Any human subjects studies without IRB approval will be automatically rejected.

Yes

Were any animal research approved by the relevant IACUC or other animal research panel? NOTE: Any animal studies without IACUC approval will be automatically rejected.

Not applicable

Please indicate which methods were used in your research:

EEG/ERP

Which processing packages did you use for your study?

Other, Please list  -   Brainstorm, OpenMEEG

Provide references using APA citation style.

1. Baillet, S., Mosher, J. C., & Leahy, R. M. (2001). Electromagnetic brain mapping. IEEE Signal processing magazine, 18, 14-30.
2. Broyd, S. J., Demanuele, C., Debener, S., Helps, S. K., James, C. J., & Sonuga-Barke, E. J. (2009). Default-mode brain dysfunction in mental disorders: a systematic review. Neurosci Biobehav Rev, 33(3), 279-296. https://doi.org/10.1016/j.neubiorev.2008.09.002
3. Haikazian, S., Chen-Li, D. C. J., Johnson, D. E., Fancy, F., Levinta, A., Husain, M. I., Mansur, R. B., McIntyre, R. S., & Rosenblat, J. D. (2023). Psilocybin-assisted therapy for depression: A systematic review and meta-analysis. Psychiatry Res, 329, 115531. https://doi.org/10.1016/j.psychres.2023.115531
4. Jensen, O., & Mazaheri, A. (2010). Shaping functional architecture by oscillatory alpha activity: gating by inhibition. Front Hum Neurosci, 4, 186. https://doi.org/10.3389/fnhum.2010.00186
5. Klimesch, W., Sauseng, P., & Hanslmayr, S. (2007). EEG alpha oscillations: the inhibition-timing hypothesis. Brain Res Rev, 53(1), 63-88. https://doi.org/10.1016/j.brainresrev.2006.06.003
6. Kometer, M., Pokorny, T., Seifritz, E., & Volleinweider, F. X. (2015). Psilocybin-induced spiritual experiences and insightfulness are associated with synchronization of neuronal oscillations. Psychopharmacology (Berl), 232(19), 3663-3676. https://doi.org/10.1007/s00213-015-4026-7
7. Pallavicini, C., Vilas, M. G., Villarreal, M., Zamberlan, F., Muthukumaraswamy, S., Nutt, D., Carhart-Harris, R., & Tagliazucchi, E. (2019). Spectral signatures of serotonergic psychedelics and glutamatergic dissociatives. Neuroimage, 200, 281-291. https://doi.org/10.1016/j.neuroimage.2019.06.053

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