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Giulia de Assis Braz

Department of Pharmaceutical Sciences, Institute of Environmental, Chemical and Pharmaceutical Sciences, Universidade Federal de São Paulo, Rua São Nicolau, 210, 1° andar, Diadema, SP, 09913-030, Brazil.

2 papers in the library · 3 citations · publishing 2025

Papers

Ketamine-Ethanol Combination Decreases Reduced Glutathione Levels and Activates both Intrinsic and Extrinsic Apoptotic Pathways Prior to Neuronal Death in SH-SY5Y Cells.

Neurotoxicity research June 7, 2025 Felype Valentim Duarte Castelhano, Carolina Aparecida de Faria Almeida, Giulia de Assis Braz et al. 3 citations

Combining ketamine with ethanol triggers greater nerve cell death than either drug alone, acting through oxidative stress and two programmed-cell-death pathways. In human neuroblastoma cells, the lowest observed adverse-effect levels were 1 mM ketamine and 100 mM ethanol. After 48 hours, the combination produced a possible synergistic increase in late apoptotic cells. Glutathione levels fell within 6 hours, and glutathione-peroxidase activity rose in all groups. Only the combination increased glutathione reductase and glutathione S-transferase activities after 3 hours, along with elevated caspase-8 and Bax expression, signaling both extrinsic and intrinsic apoptosis. The findings suggest heightened neuronal damage risk from combined use, though limitations include enzyme-activity variability, reduced sample size for some markers, and use of an immortalized cell line.

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.