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The investigators wish to investigate neurobiological effects of serotonin 2A receptor modulation in healthy volunteers, contrasting effects of an agonist (psilocybin) and an antagonist (ketanserin). Magnetic resonance imaging (MRI) and positron emission tomography (PET) will be used as neuroimaging tools.
This project applies an experimental medicine strategy coupled with human functional and molecular neuroimaging to elucidate the effects of 5-HT2A receptor (5-HT2AR) modulation on brain function and mood in healthy individuals. We compare psilocybin (5-HT2AR agonist) and ketanserin (5-HT2AR antagonist) effects on brain function to identify neural mechanisms mediating the clinical effects of psilocybin and, more broadly, to establish this comparative strategy as a pathway for delineating pharmacological effects on the brain in humans.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Project 1: Occupancy of psilocybin/ketanserin | Other | After baseline MRI & 5-HT2AR PET-imaging, participants will be allocated to undergo either one oral dose of psilocybine or one oral dose of ketanserin. After drug administration, participants will undergo two CIMBI-36 PET scans. |
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| Project 2: Long term effects of psilocybin | Other | After baseline MRI & CIMBI-36 PET-imaging, participants will receive one dose of oral psilocybine intervention. One and 12 weeks after dosing, participants will undergo post-intervention PET-scan. Subproject B: After baseline MRI & UCB-J PET-imaging, participants will receive one dose of oral psilocybine intervention. One week after dosing, participants will undergo post-intervention UCB-J PET-scan. Subproject C: After baseline MR imaging, participants will receive one dose of oral psilocybine (25 mg) or placebo. One month after dosing, participants will undergo a post-intervention MRI scan. |
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| Project 3: Functional connectivity | Other | After baseline MRI scanning and CIMBI-36 PET, participants will undergo one psilocybine-intervention fMRI scan and one ketanserin-intervention fMRI scan. If P2 shows there are long term effects of psilocybine on 5-HT2AR levels, psilocybine will be fixed as the second intervention. If not, interventions will be randomized. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Psilocybine | Drug | Oral dose of psilocybine. |
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| Measure | Description | Time Frame |
|---|---|---|
| Psilocin/ketanserin blood concentrations and 5-HT2A receptor occupancy (i.e., binding potential). | The investigators aim to model relations psilocin/ketanserin blood drug concentrations and receptor occupancy, using C11-Cimbi-36 PET imaging. | Change in Cimbi-36 binding potential from baseline PET to intervention PET 1 and PET 2 scans (same day for psilocybin, and two consecutive days for ketanserin). |
| Effects of psilocybin on Cimbi-36 binding potential at baseline and at one and twelve weeks | Cimbi-36 PET scan binding potential at baseline and at one-week post psilocybin, and potentially also at 12 weeks post psilocybin. | Change in Cimbi-36 binding potential from baseline to one week post psilocybin (and potentially also at 12 weeks after psilocybin). |
| Effects of psilocybin and ketanserin on brain function assessed with fMRI and PET | Correlations between blood levels of ketanserin and psilocin and the estimated associated receptor occupancy with functional MRI neuroimaging data, including resting state networks. Changes in synaptic density will be assessed with 11C-UCB-J PET scans before and 1 week after psilocybin intervention. | Changes in functional connectivity (fMRI) from Baseline MR to intervention MR scans for ketanserin (one or three weeks after baseline MR) and psilocybin (one or three weeks after baseline) |
| Effects of psilocybin on UCB-J binding potential at baseline and at one week | Project 2, Subproject B. UCB-J PET scan binding potential at baseline and at one-week post psilocybin. | Change in UCB-J binding potential from baseline to one week post psilocybin. |
| Effects of psilocybin on brain function assessed with fMRI at baseline and one month | Project 2, Subproject C. Resting-state and task-based fMRI measures at baseline and one month post psilocybin. |
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Inclusion Criteria:
1) Healthy individuals above 18 years of age.
Exclusion Criteria (For Subprojects 1, 2a, 2b, and 3):
Exclusion Criteria (For Subproject 2c):
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Gitte M Knudsen, Professor | Contact | +45 35456720 | gmk@nru.dk | |
| Patrick M Fisher, PhD | Contact | +45 35456714 | patrick.fisher@nru.dk |
| Name | Affiliation | Role |
|---|---|---|
| Gitte M Knudsen, Professor | Neurobiology Research Unit, Rigshospitalet | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Neurobiology Research Unit, Rigshospitalet | Recruiting | Copenhagen | 2100 | Denmark |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 42212900 | Derived | Brendstrup-Brix K, Ozenne B, Fisher PM, Stenbaek DS, Petersen AS, Armand S, McCulloch DE, Marstrand-Joergensen MR, Ulv Larsen SM, Johansen A, Jensen RH, Knudsen GM, Madsen MK. Effects of psilocybin on sleep quality and brain microstructure in chronic cluster headache. J Psychopharmacol. 2026 May 29:2698811261449380. doi: 10.1177/02698811261449380. Online ahead of print. |
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Via database of Center for Integrated Molecular Brain Imaging (Knudsen et al 2016, NeuroImage) data will be available for neuroscience research community contingent on approval by scientific board.
Upon project completion
All researchers can request access to data from the database by completing a standardized application form to provide detailed information about the specific database request. The application form and guidelines are available here. Please note that there are some formal requirements that must be fulfilled if the data request is from an international researcher. For example we do not have permission for sharing data outside of the EU, so researchers from a non-EU country will have to come here to work on the data instead.
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| ID | Term |
|---|---|
| D011562 | Psilocybin |
| D007650 | Ketanserin |
| ID | Term |
|---|---|
| D026121 | Indole Alkaloids |
| D000470 | Alkaloids |
| D006571 | Heterocyclic Compounds |
| D007211 | Indoles |
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| Ketanserin | Drug | Oral dose of ketanserin. |
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| Change in fMRI measures from baseline to one month post psilocybin |
| Anxiety Outcome Measure 1: Acute psychological effects as assessed using Challenging Experiences Questionnaire (CEQ). | Differences in CEQ scores between groups (psilocybin with music compared to psilocybin without music). Effects are measured on a Likert-scale ranging from 0 (Not all all) to 5 (Extremely; More than ever). Higher scores thus reflect a more challenging experience. Project 2, Subproject C. PsiloZonic. | Immediately post-intervention. |
| Anxiety Outcome Measure 2: Acute psychological effects as assessed using 5D-Altered States of Consciousness (5D-ASC) scale. | Differences in 5D-ASC anxiety scores between groups (psilocybin with music compared to psilocybin without music). Effects are measured on a Visual analogue scale (VAS) scale ranging from 0 (No, not more than usually) to 100 (Yes, much more than usually). Higher scores on dimension anxiety thus reflect more anxiety. Project 2, Subproject C. PsiloZonic. | Immediately post-intervention. |
| Anxiety Outcome Measure 3: Acute psychological effects as assessed using Extended Subjective Drug Intensity (eSDI) scale. | Differences in eSDI anxiety scores between groups (psilocybin with music compared to psilocybin without music). Effects are measured on a Likert-scale ranging from 0 (Not all all) to 10 (Very much). Higher scores on item anxiety thus reflect more anxiety. Project 2, Subproject C. PsiloZonic. | During intervention. |
| Transformative Experiences Outcome Measure 1: Acute psychological effects as assessed using Mystical Type Experiences Questionnaire (MEQ) scale. | Differences in MEQ scores between groups (psilocybin with music compared to psilocybin without music). Effects are measured on a Likert-scale ranging from 0 (Not all all) to 5 (Extremely). Higher scores thus reflect a more profound mystical type experience. Project 2, Subproject C. PsiloZonic. | Immediately post-intervention. |
| Transformative Experiences Outcome Measure 2: Acute psychological effects as assessed using Psychological Insights Questionnaire (PIQ) scale. | Differences in PIQ scores between groups (psilocybin with music compared to psilocybin without music). Effects are measured on a Likert-scale ranging from 0 (Not all all) to 5 (Extremely). Higher scores thus reflect more psychological insight. Project 2, Subproject C. PsiloZonic. | Immediately post-intervention. |
| Transformative Experiences Outcome Measure 3: Acute psychological effects as assessed using Emotional Breakthrough Questionnaire (EBI) scale. | Differences in EBI scores between groups (psilocybin with music compared to psilocybin without music). Effects are measured on a Visual analogue scale (VAS) scale ranging from 0 (No, not more than usually) to 100 (Yes, much more than usually). Higher scores thus reflect more emotional breakthrough. Project 2, Subproject C. PsiloZonic. | Immediately post-intervention. |
| Persisting Effects Outcome Measure 1: Persisting psychological effects as assessed using Persisting Effects Questionnaire (PEQ) scale. | Differences in PEQ scores will be assessed between groups (psilocybin with music compared to psilocybin without music). Effects are measured on a Likert-scale ranging from 0 (Not all all) to 5 (Extremely). Higher scores thus reflect more persisting effects. Project 2, Subproject C. PsiloZonic. | One and three months post-intervention. |
| D006574 |
| Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D014363 | Tryptamines |
| D054836 | Indolizidines |
| D007212 | Indolizines |
| D010880 | Piperidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D052999 | Quinazolinones |
| D011799 | Quinazolines |