Back

EEG microstate dynamics during psilocybin intoxication relate to acute experience and persisting psychological changes

Jajcay, N.; Vejmola, C.; Korcak, J.; Tyls, F.; Viktorinova, M.; Viktorin, V.; Bravermanova, A.; Androvicova, R.; Balikova, M.; Horacek, J.; Brunovsky, M.; Hlinka, J.; Palenicek, T.

2026-06-12 neuroscience
10.64898/2026.06.09.731183 bioRxiv
Show abstract

Psilocybin and other serotonergic psychedelics show therapeutic promise for psychiatric disorders, yet objective neural correlates linking the acute psychedelic state to persisting psychological outcomes remain limited. Electroencephalography (EEG) microstate analysis characterizes the rapid spatiotemporal organization of large-scale brain activity, offering a millisecond-resolution window into neural dynamics. Here, we examined resting-state EEG microstates in 15 healthy volunteers who participated in a double-blind, randomized, placebo-controlled crossover study of psilocybin, using both data-driven (three-microstate) and canonical (four-microstate) analysis solutions. EEG was recorded at five time points spanning pre-drug baseline, peak intoxication, and recovery. Psilocybin significantly increased the number of global field power (GFP) peaks and reduced microstate lifespan while increasing frequency of occurrence during peak intoxication (50-100 min post-administration), consistent with accelerated transitions between brain states. Notably, microstate coverage was largely preserved, with only a transient difference at peak intoxication in the 2-20 Hz band-width, suggesting that access to the repertoire of canonical brain states is broadly maintained despite altered temporal dynamics. Critically, individual differences in microstate dynamics during peak intoxication correlated with both acute subjective experience intensity and self-reported psychological changes measured 28 days post-administration, providing exploratory evidence for a link between acute neural dynamics and longer-term experiential outcomes in healthy volunteers. These findings suggest that psilocybin is associated with altered temporal organization of large-scale brain dynamics with largely preserved microstate coverage, and identify EEG microstates as candidate neural markers for psychedelic-induced alterations in consciousness with potential relevance to therapeutic research.

Matching journals

The top 7 journals account for 50% of the predicted probability mass.

1
Neuropsychopharmacology
153 papers in training set
Top 0.2%
11.7%
2
Translational Psychiatry
260 papers in training set
Top 0.3%
11.7%
3
Psychopharmacology
69 papers in training set
Top 0.2%
6.6%
4
NeuroImage
903 papers in training set
Top 2%
6.6%
5
Molecular Psychiatry
282 papers in training set
Top 1.0%
6.6%
6
The Journal of Neuroscience
1025 papers in training set
Top 3%
5.4%
7
Biological Psychiatry: Cognitive Neuroscience and Neuroimaging
71 papers in training set
Top 0.4%
4.8%
50% of probability mass above
8
Journal of Psychopharmacology
17 papers in training set
Top 0.1%
3.2%
9
Scientific Reports
3612 papers in training set
Top 38%
2.7%
10
Progress in Neuro-Psychopharmacology and Biological Psychiatry
48 papers in training set
Top 0.3%
2.4%
11
Nature Communications
5641 papers in training set
Top 42%
2.1%
12
European Neuropsychopharmacology
20 papers in training set
Top 0.1%
2.1%
13
Psychological Medicine
88 papers in training set
Top 1%
1.9%
14
Neuropharmacology
68 papers in training set
Top 0.5%
1.7%
15
Biological Psychiatry Global Open Science
60 papers in training set
Top 0.8%
1.7%
16
eLife
5828 papers in training set
Top 49%
1.7%
17
Biological Psychiatry
137 papers in training set
Top 2%
1.7%
18
Imaging Neuroscience
282 papers in training set
Top 3%
1.5%
19
ACS Chemical Neuroscience
67 papers in training set
Top 0.8%
1.5%
20
Psychophysiology
77 papers in training set
Top 1%
1.0%
21
Communications Biology
993 papers in training set
Top 25%
1.0%
22
Proceedings of the National Academy of Sciences
2444 papers in training set
Top 37%
1.0%
23
Advanced Science
286 papers in training set
Top 8%
1.0%
24
Neurobiology of Disease
148 papers in training set
Top 3%
0.9%
25
Addiction Biology
51 papers in training set
Top 0.6%
0.8%
26
eneuro
439 papers in training set
Top 8%
0.8%
27
American Journal of Psychiatry
24 papers in training set
Top 0.6%
0.8%
28
Journal of Affective Disorders
92 papers in training set
Top 2%
0.6%
29
British Journal of Pharmacology
40 papers in training set
Top 1%
0.6%
30
PLOS ONE
5266 papers in training set
Top 65%
0.6%