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Daniela Aparecida Chagas‐paula

Universidade Federal de Alfenas

2 papers in the library · 9 citations · publishing 2022-2025

Papers

Immunological Modulation and Control of Parasitaemia by Ayahuasca Compounds: Therapeutic Potential for Chagas's Disease

Chemistry & Biodiversity September 26, 2022 Albert Katchborian‐neto, Mário F. C. Santos, Diego Fernandes Vilas Boas et al. 9 citations

Ayahuasca, a psychoactive beverage made from Banisteriopsis caapi and Psychotria viridis, showed moderate activity against Trypanosoma cruzi trypomastigotes in vitro (IC50 95.78 μg/mL), compared to the reference drug benznidazole (IC50 2.03 μg/mL). The β-carboline alkaloid harmine, isolated from B. caapi, was active (IC50 6.37 μg/mL), while the tryptamine DMT from P. viridis was moderately active (IC50 21.02 μg/mL). In vivo, harmine alone reduced parasitemia in a dose-responsive manner (10 and 100 mg/kg) without toxic effects. Ayahuasca and the harmine-DMT combination worsened parasitemia, suggesting immune modulation via increased IgG and IgG1 antibodies. Molecular docking indicated harmine binds to trypanothione reductase, a promising drug target absent in humans. The findings support ayahuasca's potential against Chagas disease and internal parasites.

Dimethyltryptamine and harmine, components of ayahuasca, prevented cocaine-induced apoptosis in SH-SY5Y human neuroblastoma cells

Archives of Toxicology November 12, 2025 Gilles Salles, Carolina Aparecida de Faria Almeida, Isabella de Carvalho Alves et al.

Ayahuasca compounds N,N-dimethyltryptamine (DMT) and harmine (HRE), both alone and combined, partially protected human SH-SY5Y neuroblastoma cells from cocaine-induced toxicity. Cells exposed to cocaine with DMT and/or HRE showed increased viability compared to cocaine-only groups. Flow cytometry indicated partial to complete protection against apoptosis, and western blot revealed reduced expression of the apoptosis marker caspase-8 in co-treated cells. These findings suggest Ayahuasca-derived alkaloids merit further research for neuroprotection and treatment of substance use disorders.