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Ego dissolution as a collapse of integration, not a surge of entropy

Sören van Krunckelsven

Zenodo (CERN European Organization for Nuclear Research) June 18, 2026 DOI: 10.5281/zenodo.20751383 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Computational modeling study (dynamic mean-field model) Peer reviewed
Population Human structural connectomes (empirical)
Topics Ego dissolution
Keywords Nmda receptor Control theory sociology Noise video Agonist Statistical physics Mathematical analysis
Key points In the model, the combined serotonergic–dissociative state is dissociation-dominated: the brain loses its capacity to integrate, not its local richness.

Abstract

AbstractThe “entropic brain” hypothesis holds that psychedelic and other ego-dissolving states correspondto an increase in the entropy or signal diversity of spontaneous brain activity. Motivated by afirst-person report of a combined serotonergic–dissociative state (LSD/DMT together with nitrousoxide, N2O), we asked a sharper question: when a 5-HT2A agonist and an NMDA antagonist acttogether, is the resulting state dominated by a rise in local signal complexity, by a collapse of longrange functional integration, or by both? We address this in a validated whole-brain dynamicmean-field (DMF) model (reduced Wong–Wang, Deco et al. 2014) implemented in The VirtualBrain, on empirical human structural connectomes, with regional excitation/inhibition balancedby analytic Feedback Inhibition Control (FIC). The two drug classes are represented by separable,biophysically motivated parameters: 5-HT2A agonism as a density-weighted increase in excitatoryresponse gain, and sub-anaesthetic NMDA antagonism as interneuron-preferential disinhibition(reduced excitatory→inhibitory NMDA conductance) plus reduced long-range NMDA coupling.Crucially, because both perturbations shift mean firing rate — and both Lempel–Ziv complexity(LZc) and functional connectivity (FC) co-vary with rate — we rate-match every condition backto the ∼3 Hz physiological set-point before reading out the metrics, isolating mechanism from atrivial rate confound. At matched rate, the combination produces a robust, dose-dependent,topology-general collapse of functional integration (mean ΔFC = −56%±12% SD, negative in 6/6 noise seeds and reproduced on a second 192-region connectome) together with a smallbut statistically reproducible increase in signal complexity (ΔLZc = +0.9%±0.5% SD,positive in 6/6 seeds, 𝑡 ≈ 4). These multi-seed values are the canonical results; single-run figuresquoted in the development log are individual noise realisations. The 5-HT2A entropy increase(+5.4%) is largely cancelled by an N2O-driven hypersynchrony (−4.6%), so the net complexitychange is marginal while the integration collapse is large. We conclude that, in this model, thecombined ego-dissolving state is dissociation-dominated rather than entropy-dominated:the brain loses its capacity to integrate, not its local richness. We discuss this as a refinement ofthe entropic-brain framing for combined serotonergic–dissociative states, and report the analysestransparently including a working-point artefact we explicitly reject.Keywords: ego dissolution, entropic brain, dynamic mean-field model, The Virtual Brain, feedback inhibition control, 5-HT2A, NMDA antagonist, nitrous oxide, functional integration, LempelZiv complexity