A single psilocybin dose is associated with long-term increased mindfulness, preceded by a proportional change in neocortical 5-HT2A receptor binding

This open-label study (n=10) found a significant increase in mindfulness (MAAS) and openness (NEO PI-R) after a single high dose (14-21mg) of psilocybin.

Abstract

“A single dose of the serotonin 2A receptor (5-HT2AR) agonist psilocybin can have long-lasting beneficial effects on mood, personality, and potentially on mindfulness, but underlying mechanisms are unknown. Here, we for the first time conduct a study that assesses psilocybin effects on cerebral 5-HT2AR binding with [11C]Cimbi-36 positron emission tomography (PET) imaging and on personality and mindfulness. Ten healthy and psychedelic-naïve volunteers underwent PET neuroimaging of 5-HT2AR at baseline (BL) and one week (1W) after a single oral dose of psilocybin (0.2–0.3 mg/kg). Personality (NEO PI-R) and mindfulness (MAAS) questionnaires were completed at BL and at three-months follow-up (3M). Paired t-tests revealed statistically significant increases in personality Openness (p-uncorrected = 0.04, mean change [95%CI]: 4.2[0.4;∞]).”

Authors: Martin Korsbak Madsen, Patrick MacDonald Fisher, Dea Siggaard Stenbæk, Sara Kristiansen, Daniel Burmester, Szabolcs Lehel, Tomas Páleníček, Martin Kuchar, Claus Svarer, Brice Ozenne & Gitte M. Knudsen

Notes

This paper gives further evidence for psychedelics having the ability to change your personality (at 3 months follow-up in this case). This is corroborated by Maclean et al. (2011), who found a similar result.

Noted should be that although it’s statistically significant, the change is from 127 (16.6 standard deviation), to 131 (17.2), so the total change is quite small (3%).

Summary

Psilocybin can have long-lasting beneficial effects on mood, personality, and potentially on mindfulness. Here, we assess psilocybin effects on cerebral 5-HT2AR binding with [ 11 C]Cimbi-36 positron emission tomography and on personality and mindfulness.

2.1. Participants

Ten healthy volunteers without prior intake of psychedelic drugs were recruited from a list of participants that expressed interest in participating in a psilocybin brain scanning study. They underwent screening for somatic illness, neurological condition/disease, significant somatic condition/disease, and psychiatric disorders.

2.2. Procedures

Participants were informed about the study, its safety precautions, potential effects and side-effects of psilocybin, and filled out questionnaires before undergoing neuroimaging with [ 11 C]Cimbi-36 PET and MRI. One week after psilocybin, participants underwent neuroimaging with [ 11 C]Cimbi-36 PET and MRI.

2.3. Psychometric evaluations

Participants completed the 11-dimension Altered States of Consciousness questionnaire, the revised Mystical Experiences Questionnaire, and the Ego-Dissolution Inventory at the end of psilocybin session days, and the Persistent Effects Questionnaire at three-months follow-up.

2.4. [ 11 C]Cimbi-36 PET acquisition

[11 C]Cimbi-36 PET imaging was acquired for 120 min after a bolus injection on a high-resolution research tomograph (HRRT) PET-scanner (CTI/Siemens, Knoxville, USA).

2.5. [ 11 C]Cimbi-36 PET image processing and kinetic modeling

We extracted regional time-activity curves from 42 cortical and subcortical regions and used the simplified reference tissue model (SRTM) for kinetic modeling. The non-displaceable binding potential (BP ND) is proportional to the number of 5-HT2ARs available for binding.

2.6. Magnetic resonance imaging

MRI data was acquired on a 3T Prisma scanner using a 64-channel head coil. High resolution 3D T1- and T2-weighted images were acquired for the purpose of PET-image processing as recently described.

2.7. Data analysis

Neocortex was selected as region of interest in the statistical evaluation of changes in [ 11 C]Cimbi-36 BP ND following psilocybin due to the high expression of 5-HT2ARs in cortex. Post hoc exploratory paired t-tests were performed on the 14 bilateral cortical regions.

Openness, Conscientiousness, Extraversion, Agreeableness and Neuroticism were tested for increase after psilocybin, and the relationship between change in [ 11 C]Cimbi-36 BP ND and change in MAAS and Openness was evaluated using post hoc linear regressions.

Authors

Authors associated with this publication with profiles on Blossom

Tomáš Páleníček
Tomas Palinek is a researcher and psychiatrist in the Czech Republic where he studies a variety of psychedelics at the NIHM.

Linked Research Papers

Notable research papers that build on or are influenced by this paper

Subacute effects of a single dose of psilocybin on biomarkers of inflammation in healthy humans: An open-label preliminary investigation
This open-label study (n=16) assessed the effects of a single dose of psilocybin (15mg/70kg) on biomarkers of inflammation in healthy participants. Blood samples before and one day after the administration revealed that psilocybin did not significantly impact any of the selected biomarkers.

Lasting increases in trait mindfulness after psilocybin correlate positively with the mystical-type experience in healthy individuals
This open-label study (n=39) assessed the association between psilocybin lasting increases in trait mindfulness and the mystical-type experience using the Mystical Experience Questionnaire (MEQ). The MEQ was administered after psilocybin sessions (16-22mg/70kg), and mindfulness was measured three months post-session using the Mindful Attention and Awareness Scale (MAAS). MAAS score was significantly increased at the 3-month follow-up. It was positively associated with the MEQ score (p = 0.035), indicating that the phenomenology of the psilocybin experience induces a shift toward mindful living.