Global increases in brain glucose metabolism following acute N,N-dimethyltryptamine and harmine administration in healthy volunteers: A randomised [ 18 F]FDG-PET study
Klemens Egger, Robert Bozsak, Helena D Aicher, Hasan Sari, Sandra N. Poetzsch, Axel Rominger, C. Martin-Soelch, John W Smallridge, Dario Dornbierer, Boris B. Quednow, Milan Scheidegger, P. Cumming
Universität Zürich, ZORA June 1, 2026 DOI: 10.5167/uzh-434709 via OpenAlex
Summary
AI-generated from the abstractA psychedelic dose of DMT combined with the MAO-A inhibitor harmine, mimicking ayahuasca, globally increased cerebral glucose metabolism by 12.5% compared to placebo in 14 healthy males. Scans acquired during peak drug effects using FDG-PET showed widespread cortical increases, particularly in higher-order brain networks. Higher harmine plasma levels correlated with greater global glucose metabolism, while DMT levels and subjective intensity did not. This metabolic signature recapitulates a classic finding for psilocybin, suggesting a potential hallmark of the psychedelic state.
Study at a glance
| Characteristics | Single-blind crossover study Randomized Peer reviewed |
|---|---|
| Sample size | 14 |
| Population | Healthy males |
| Keywords | Harmine Placebo Neuroimaging Metabolite Electroencephalography |
| Registration | NCT06252506 |
| Key finding | DMT plus harmine globally increased cerebral glucose metabolism by 12.5% versus placebo, with harmine plasma levels positively correlating with the increase. |
Abstract
Classical psychedelics such as N,N -dimethyltryptamine (DMT) modulate consciousness via serotonergic receptor agonism, and are increasingly investigated for their psychotherapeutic potential. When combined with the monoamine oxidase A (MAO-A) inhibitor harmine—mimicking the pharmacological profile of ayahuasca—oral DMT induces a psychedelic experience lasting 4–5 h. While some neuroimaging studies have characterized effects of DMT on functional connectivity and electroencephalography its impact on cerebral energy metabolism remains largely unexplored. We assessed the cerebral metabolic rate for glucose consumption (CMRglc) with [ $^{18}$ F]fluorodeoxyglucose positron emission tomography ([ $^{18}$ F]FDG-PET) and linear graphic analysis following buccal DMT + harmine (90 mg DMT, 120 mg harmine) versus placebo in a single-blind, crossover design in 14 healthy males. Scans were acquired during peak drug effects (100–170 min post-administration). Global CMRglc increased by 12.5% under DMT+harmine versus placebo ( t = 2.58, p = 0.011). Vertex- and network-wise analyses revealed widespread cortical increases, particularly in higher-order brain networks. Exploratory analyses found a significant positive correlation between global CMRglc and harmine plasma levels, but not with DMT plasma levels, subjective intensity ratings. A psychedelic dose of DMT + harmine globally increased cerebral glucose metabolism, recapitulating a classic finding for psilocybin, and suggesting a potential metabolic signature of the psychedelic state. Clinical trial registry name and URL incl. registration number: Molecular Imaging Study of Harmine/DMT: a Basic Research Approach (HaD-PET) https://clinicaltrials.gov/study/NCT06252506 .