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Tibor M. Brunt

Trimbos Institute

3 papers in the library · 295 citations · publishing 2010-2025

Papers

Instability of the ecstasy market and a new kid on the block: mephedrone

Journal of Psychopharmacology September 8, 2010 Tibor M. Brunt, Anneke Poortman, Raymond J.m. Niesink et al. 217 citations

The ecstasy market in the Netherlands became unstable in 2009, with more than a 50% drop in tablets containing MDMA. A new substance, mephedrone, partially replaced MDMA in tablets sold as ecstasy, at doses between 96 and 155 mg. Based on reports from 70 regular ecstasy users, mephedrone produced enjoyable effects similar to other amphetamine-type stimulants, including MDMA, but unlike MDMA it induced strong cravings in most users. If the unstable market continues, mephedrone may substantially substitute for MDMA, raising health concerns.

How toxic is ibogaine?

Clinical toxicology (Philadelphia, Pa.) January 1, 2016 Ruud P. W. Litjens, Tibor M. Brunt 74 citations

Ibogaine, a psychoactive alkaloid from the African shrub Tabernanthe iboga, is unlicensed but used to treat addiction. It is metabolized mainly by CYP2D6 to noribogaine, which persists for days. Both compounds interact with multiple neurotransmitter systems. In rats, neurotoxicity occurs at doses above 25 mg/kg intraperitoneal, likely via excitotoxic effects on cerebellar Purkinje cells. Cardiotoxicity arises from blockade of hERG potassium channels, prolonging the QT interval and causing arrhythmias and sudden cardiac arrest. Twenty-seven fatalities have been reported; eight case studies show ventricular tachyarrhythmias in individuals without pre-existing heart conditions. Noribogaine appears at least as cardiotoxic as ibogaine. CYP2D6 polymorphism and concurrent medications increase risks. Without medical supervision, further deaths are likely.

Above the threshold, beyond the trip: the role of the 5-HT2A receptor in psychedelic-induced neuroplasticity and antidepressant effects

Molecular Psychiatry August 23, 2025 Adam J. Drewko, Ron L. P. Habets, Tibor M. Brunt 4 citations

Serotonergic psychedelics like psilocybin and LSD show promise for treatment-resistant depression by rapidly inducing neuroplasticity, but the molecular mechanisms are debated. This narrative review examines evidence on whether the serotonin 5-HT2A receptor, which mediates hallucinogenic effects, is also required for neuroplasticity. It covers how decreased neuroplasticity relates to depression, how psychedelics promote dendrito-, spino-, and synaptogenesis, and whether these effects are regionally selective. The review critically assesses conflicting studies on the necessity of 5-HT2A signaling for neuroplastic effects and presents a model of the molecular mechanisms involved.