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Ricardo Jorge Dinis-Oliveira

IINFACTS-Institute of Research and Advanced Training in Health Sciences and Technologies, Department of Sciences, University Institute of Health Sciences (IUCS), CESPU, CRL, 4585-116 Gandra, Portugal.

5 papers in the library · 221 citations · publishing 2017-2026

Papers

Metabolism of psilocybin and psilocin: clinical and forensic toxicological relevance

Drug Metabolism Reviews January 2, 2017 Ricardo Jorge Dinis-Oliveira 221 citations

Psilocybin and psilocin, the main hallucinogenic compounds in magic mushrooms, act as agonists or partial agonists at 5-HT2A receptors. Psilocybin is a pro-drug dephosphorylated by alkaline phosphatase to the active metabolite psilocin, which is further metabolized; psilocin-O-glucuronide is the main urinary metabolite with clinical and forensic relevance. Considerable physiological variability between individuals influences dose-response and toxicological profiles. The review presents all major and minor psychoactive metabolites of psilocybin and psilocin.

Impact of psilocybin and Psilocybe cubensis extract on gut microbiota in Wistar Han rats

Science Letters April 17, 2026 Francisco Sacadura, Cláudia Marques, Andreia Machado Brito-Da-Costa et al.

Both pure psilocybin and a Psilocybe cubensis extract altered the gut microbiota of male Wistar Han rats over two weeks. Fecal samples analyzed by 16S rRNA amplicon sequencing showed that microbial community structure shifted away from baseline and control profiles at day 7 and diverged further by day 14. The effect was more pronounced in rats given pure psilocybin than in those given the whole mushroom extract, suggesting the extract's additional compounds may modulate the impact. The results indicate a time-dependent modulation of gut microbiota by both treatments, with differential magnitude between the pure compound and the whole extract.

Investigating Psychedelic Tryptamines: Extraction and Quantification from Psilocybe Mushrooms

Science Letters April 17, 2026 Beatriz P. Senra, Ricardo Jorge Dinis-Oliveira, Carlos J. A. Ribeiro

Psilocybe cubensis mushrooms contain psilocybin (0.5%–1.5% in dried mushrooms) and psilocin, which have therapeutic potential and are used recreationally. An optimized extraction method using cold methanol with 10% water and kinetic maceration yielded 1.98% psilocybin and 0.10% psilocin. A thin-layer chromatography (TLC) method with Ehrlich's reagent was developed for rapid identification of these tryptamines, suitable for forensic applications.

Psilocybin and Psilocybe cubensis extract exhibit divergent behavioural and toxicological effects in rats

Science Letters April 17, 2026 Diana Dias Da Silva, Andreia Machado Brito-Da-Costa, Francisco Sacadura et al.

Pure psilocybin and whole Psilocybe cubensis extract produce distinct behavioral and toxicological effects in male Wistar Han rats. Pure psilocybin decreased conditioned place preference scores at days 1 and 7, indicating aversive or non-reinforcing effects, and reduced exploratory activity. The extract did not significantly alter preference but transiently increased exploratory behavior at day 7. Peripherally, pure psilocybin increased relative liver weight, suggesting hepatic stress, while the extract reduced renal lipid peroxidation, indicating a protective or antioxidant effect likely from other compounds. These differences highlight the importance of matrix effects in psychedelic research.

Neurotoxic and Neuroprotective Effects of Psychedelics in a Human Neuroblastoma Cell Model

RevSALUS - Revista Científica da Rede Académica das Ciências da Saúde da Lusofonia January 1, 2025 Andreia Machado Brito Da Costa, Ricardo Jorge Dinis-Oliveira, Áurea Madureira-Carvalho et al.

Psychedelic compounds such as LSD, psilocin, psilocybin, 5-MeO-DMT, and mescaline show distinct neurotoxicity profiles in human neuroblastoma cells. LSD was the most cytotoxic, with EC50 values of 0.23 mM (MTT) and 0.57 mM (NR), while psilocin showed moderate toxicity (EC50 0.42 mM MTT, 0.69 mM NR). Psilocybin did not reach an EC50 within the tested range, indicating minimal toxicity. 5-MeO-DMT and mescaline affected cell viability only at higher concentrations (EC50 1.17–1.69 mM). Pre-treatment with any of these compounds did not significantly protect against glutamate-induced toxicity, suggesting limited neuroprotective potential in this model.