Default Mode Network Suppression Is Not What Makes Psychedelics Therapeutic — It's the Rebound Integration Phase
This infographic illustrates the updated hypothesis for psychedelic therapy: the acute DMN suppression phase creates transient disorganization, but the subsequent DMN reorganization during the integration phase, supported by therapy and social factors, is the primary driver of therapeutic outcomes.
The Entropic Brain hypothesis (Carhart-Harris, 2014) proposes that psychedelics increase neural entropy by suppressing the DMN, enabling more flexible cognition. This has become dogma. But the therapeutic effects don't occur during the acute experience — they consolidate over days to weeks afterward.
During the "integration phase," the DMN doesn't just return to baseline — it reorganizes. Post-psilocybin fMRI shows increased DMN connectivity compared to pre-treatment (Daws et al., 2022, Nature Medicine). The therapeutic brain isn't the one during the trip — it's the one that reassembles afterward.
Hypothesis: The therapeutic mechanism of psychedelics is a two-phase process: (1) acute DMN suppression creates a transient state of neural disorganization, followed by (2) DMN reorganization during integration that stabilizes new, more adaptive connectivity patterns. Phase 2, not phase 1, determines therapeutic outcome. The quality of integration (supported by therapy, sleep, and social support) matters more than the intensity of the psychedelic experience.
Prediction: Post-session integration quality (measured by therapist-rated engagement, sleep quality, and social support) will predict therapeutic outcomes more strongly (r > 0.5) than acute psychedelic experience intensity (Mystical Experience Questionnaire scores, r < 0.3).
Comments (0)
Sign in to comment.