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Nelson G. M. Gomes

5 papers in the library · 156 citations · publishing 2020-2026

Papers

Toxicokinetics and Toxicodynamics of Ayahuasca Alkaloids N,N-Dimethyltryptamine (DMT), Harmine, Harmaline and Tetrahydroharmine: Clinical and Forensic Impact.

Pharmaceuticals (Basel) October 23, 2020 Andreia Machado Brito-Da-Costa, Diana Dias Da Silva, Nelson G. M. Gomes et al. 111 citations

Ayahuasca's psychoactive effects stem from the interplay of its alkaloids: N,N-dimethyltryptamine (DMT), harmine, harmaline, and tetrahydroharmine. DMT is rapidly absorbed and metabolized, but its oral activity requires monoamine oxidase inhibition by β-carbolines (harmine, harmaline) to prevent breakdown. Harmine and harmaline are quickly metabolized, while tetrahydroharmine has a longer half-life. The pharmacokinetics and pharmacodynamics of these compounds influence the duration and intensity of subjective effects, as well as potential toxicity. Understanding these processes is crucial for clinical management of adverse reactions and for forensic interpretation in cases of intoxication or death.

Pharmacokinetics and Pharmacodynamics of Salvinorin A and Salvia divinorum: Clinical and Forensic Aspects

Pharmaceuticals February 3, 2021 Andreia Machado Brito-Da-Costa, Áurea Madureira-Carvalho, Diana Dias Da Silva et al. 42 citations

Salvia divinorum, a mint from Mexico used for centuries by Mazatecans for divinatory and medicinal purposes, is increasingly used recreationally by adolescents and young adults. Its main psychoactive compound, salvinorin A, is a non-nitrogenous diterpenoid that acts selectively on the κ-opioid receptor. Absorption occurs through oral mucosa or respiratory tract; when swallowed, it is rapidly broken down in the gastrointestinal system to its inactive metabolite salvinorin B. The compound is quickly distributed, accumulates in the brain, and is rapidly eliminated, matching its short-lived effects. No reports of toxicity or serious adverse outcomes were found. Proposed therapeutic applications include treatment of chronic pain, gastrointestinal and mood disorders, neurological diseases, and drug dependence, but clinical acceptance is limited by psychotropic side effects and misuse.

Mexican calea (Calea zacatechichi Schltdl.) interferes with cholinergic and dopaminergic pathways and causes neuroglial toxicity.

Journal of Ethnopharmacology January 30, 2025 Maria Rita Garcia, Federico Ferreres, Tiago Mineiro et al. 3 citations

An aqueous extract of the aerial parts of Calea zacatechichi, a plant traditionally used for its dream-inducing effects, interferes with the cholinergic and dopaminergic systems by inhibiting acetylcholinesterase and tyrosinase, but does not affect monoamine oxidase A. The extract also shows notable cytotoxicity in neuronal and microglial cells at low concentrations, with evidence of apoptosis and necroptosis, though it scavenges free radicals and inhibits lipid peroxidation. Twenty-eight phenolic constituents were identified, 24 previously unreported in this species. The findings highlight the need for a regulatory framework for recreational use and help clarify the plant's psychopharmacological mechanisms.

In vitro neuronal characterization of the entheogenic plant Tagetes lucida Cav.

Science Letters April 11, 2026 Maria Eduarda Bertino Nahim Garcia, Ema Santos, Diana Dias Da Silva et al.

An aqueous extract of Tagetes lucida aerial parts, a plant used traditionally by Mesoamerican tribes and now recreationally for its psychoactivity, contains phenolic acids, coumarins, and flavonoids, mainly scoparone and herniarin. In human neuroblastoma cells, the extract caused mitochondrial depolarization starting at 250 µg/mL and impaired cell metabolism and membrane integrity at the highest concentration tested (1000 µg/mL). However, when cells were exposed to glutamate, the extract showed neuroprotection at concentrations from 62.5 to 250 µg/mL, counteracting excitotoxic effects. The extract also inhibited acetylcholinesterase and monoamine oxidase A in a concentration-dependent manner, suggesting neuromodulatory properties. These results highlight both neurotoxic and neuroprotective effects, warranting further study.

Rare but relevant: MDMA and hyponatraemia

Addiction December 8, 2025 María Rita Concepción García, Nelson G. M. Gomes, Diana Dias Da Silva

MDMA (ecstasy), commonly used for its stimulant and empathogenic effects especially among young adults in recreational settings, can cause hyponatraemia—a low blood sodium concentration that alters mental state and is life-threatening if untreated. Although hyponatraemia is a common electrolyte disorder in clinical care, acute MDMA-induced hyponatraemia was first reported in 1993. Women face higher incidence rates and greater odds of severe effects. This review describes the clinical manifestations, prevalence, pathophysiological mechanisms, and therapeutic approaches for correcting this electrolyte imbalance.