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Marcus Herdener

9 papers in the library · 123 citations · publishing 2017-2026

Papers

Serotonin 2A Receptor Signaling Underlies LSD-induced Alteration of the Neural Response to Dynamic Changes in Music

Cerebral Cortex September 12, 2017 Frederick S. Barrett, Katrin H. Preller, Marcus Herdener et al. 52 citations

Classic psychedelic drugs that activate serotonin 2A receptors alter how the brain responds to the changing tonal structure of music. In 25 healthy adults, brain imaging after placebo, LSD, and LSD combined with a serotonin 2A blocker showed that serotonin 2A signaling changes neural activity in regions for basic and higher-level music processing, memory, emotion, and self-referential thought. This signaling appears critical for tracking musical tonality and for the heightened emotionality, connectedness, and meaningfulness people often report after taking psychedelics. The findings clarify the neuropsychopharmacology of music perception and why music can feel profoundly altered during psychedelic experiences.

Psilocybin-assisted therapy for relapse prevention in alcohol use disorder: a phase 2 randomized clinical trial

EClinicalMedicine March 14, 2025 Raoul Bitar, Simon Halm, Christina Rossgoderer et al. 42 citations

A randomized controlled trial investigated whether psilocybin-assisted therapy could reduce relapse in patients with alcohol use disorder. The study compared psilocybin therapy against a control condition, finding that the psilocybin group showed a significantly lower rate of heavy drinking days over the follow-up period. The results suggest that psilocybin, when combined with psychotherapy, may be a promising intervention for relapse prevention in alcohol dependence, though further research is needed to confirm these findings.

Neural underpinnings of prosexual effects induced by gamma-hydroxybutyrate in healthy male humans

European Neuropsychopharmacology March 8, 2017 Oliver G. Bosch, Michael M. Havranek, A Baumberger et al. 22 citations

Gamma-hydroxybutyrate (GHB), a drug used for narcolepsy and abused recreationally, has prosexual effects in healthy men. In two double-blind, placebo-controlled experiments, GHB increased subjective sexual arousal and desire, and made sexually neutral images of people seem arousing. Brain scans showed that GHB boosted activity in reward regions like the nucleus accumbens when viewing erotic pictures, and increased connectivity between the nucleus accumbens and the ventromedial prefrontal cortex. The findings indicate GHB enhances hedonic sexual functioning and lowers the threshold for perceiving erotic cues by sensitizing mesolimbic reward pathways.

The emotional architecture of the psychedelic brain

Trends in Cognitive Sciences August 18, 2025 Flora Moujaes, Nathalie M. Rieser, L. Belinger et al. 5 citations

Serotonergic psychedelics are being investigated as treatments for psychiatric conditions, with promising results in mood disorders suggesting their effects on emotional processing may be central to therapeutic potential. However, mechanistic and clinical studies reveal a complex picture of how psychedelics impact emotions and mood. This review covers recent findings on psychedelics' effects on emotion, emotional empathy, and mood, discussing their influence on long-term emotion management strategies, the role of challenging experiences, and neuroplastic changes. The authors argue that more precise characterization of emotional states and attention to temporal dynamics of psychedelic-induced effects are critical for clarifying mechanisms and optimizing therapeutic impact.

Epigenome-wide association study of psilocybin-induced methylome changes in alcohol use disorder.

Translational psychiatry May 26, 2026 Marvin M Urban, Lea Zillich, Nathalie M Rieser et al. 1 citation

In a pilot study of 37 detoxified patients with alcohol use disorder, psilocybin (25 mg) produced changes in DNA methylation across the genome compared to placebo. One methylation site in the TLE4 gene and a differentially methylated region in RASGRP4 were linked to psilocybin treatment. Co-methylation networks related to psilocybin were associated with reductions in depressive symptoms and drinking behavior, and gene analysis pointed to involvement in neuroplasticity and immune functions. The primary trial endpoints—duration of abstinence and mean alcohol use—were not reached, so the analysis focused on secondary psychometrics. The findings suggest immunomodulatory actions of psilocybin but are limited by the modest sample size.

Co-Boost: boosting and guiding neuroplasticity by combining ketamine with neurofeedback-assisted learning—towards an individualised and integrated pharmaco-psychotherapy for cocaine addiction: study protocol for a randomised, placebo-controlled, double-blind, parallel-group, single-centre trial

Trials September 25, 2025 Anna Trippel, Ladina P Gubser, Etna Engeli et al. 1 citation

Cocaine is the most frequently used stimulant worldwide, with increasing consumption in Europe. Psychotherapeutic interventions for cocaine use disorder (CUD) show only modest effects, and no pharmacotherapy has been approved. A novel target, glutamatergic neurotransmission, emerged from animal models: after chronic cocaine, glutamate concentrations in the nucleus accumbens are reduced, with overflow during cue-induced cocaine-seeking. This imbalance has also been observed in humans. Neurofeedback training (NFT) studies using real-time functional magnetic resonance imaging (rt-fMRI) show participants with CUD can learn to regulate brain activity in reward areas using reward imagery.

Epigenome-wide Association Study of Psilocybin-Induced Methylome Changes in Alcohol Use Disorder

July 18, 2025 Marvin M. Urban, Eric Zillich, Nathalie M. Rieser et al. preprint

A single dose of psilocybin (25 mg) was associated with changes in DNA methylation in patients with alcohol use disorder. One methylation site in the TLE4 gene and a region in the RASGRP4 gene showed significant alterations. Co-methylation networks linked to psilocybin treatment were also associated with reduced depressive symptoms and drinking behavior, and involved genes related to neuroplasticity and immune function. Baseline methylation differences between treatment responders and non-responders appeared in genes related to synaptic plasticity and neurotransmitter systems. The findings are preliminary due to the small sample size but align with prior research and suggest possible biological pathways for psilocybin's therapeutic effects.

Ketamine-induced changes in accumbal glutamate and their association with altered states of consciousness.

Brain research bulletin May 1, 2026 Ladina Philomena Gubser, Anna Stefania Trippel, Niklaus Zoelch et al.

A single intravenous dose of R,S-ketamine (0.71 mg/kg bodyweight) administered over 40 minutes to 10 healthy volunteers did not significantly increase glutamate levels in the nucleus accumbens (NAc) when measured by proton magnetic resonance spectroscopy. However, individual changes in glutamate were positively associated with anxious ego dissolution and reductions in vigilance, suggesting that ketamine-induced glutamate alterations in the NAc may underlie specific alterations in perception and consciousness.

Co-Boost: Boosting and guiding neuroplasticity by combining ketamine with neurofeedback-assisted learning – towards an individualised and integrated pharmaco-psychotherapy for cocaine addiction: study protocol for a randomised, placebo-controlled, double-blind, parallel-group, single-centre trial

Anna Stefania Trippel, Ladina Philomena Gubser, Etna Jennifer Elektra Engeli et al.

A randomized, placebo-controlled, double-blind trial will test a single ketamine infusion, three sessions of reward-imagery real-time fMRI neurofeedback training, and their combination in 120 people with cocaine use disorder. The study expects both interventions to reduce the proportion of cocaine use days, with ketamine increasing glutamate in the reward system and lowering craving, and neurofeedback re-sensitizing participants to natural rewards. This neurobiologically informed approach aims to open new treatment avenues through individualized pharmaco-psychotherapy.