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Rodrigo Portes Ureshino

Department of Biological Sciences, Universidade Federal de São Paulo, Diadema, SP, Brazil.

2 papers in the library · 3 citations · publishing 2025-2026

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.

Editorial: Psychedelic substances and neurological diseases: from basics to clinical application

Frontiers in Pharmacology March 16, 2026 Alessandra Linardi, Ariadiny Lima Caetano, Rodrigo Portes Ureshino

Scientific interest in psychedelic substances has revived, offering new perspectives on treating neuropsychiatric and neurological disorders. Psychedelics induce neuroplasticity and alleviate symptoms of depression, anxiety, PTSD, and neurodegenerative diseases like Alzheimer's and Parkinson's. A review of six abused recreational drugs—methamphetamine, cocaine, synthetic cathinones, ketamine, nitrous oxide, and heroin—shows they share convergent neurotoxic mechanisms involving oxidative stress, mitochondrial dysfunction, excitotoxicity, and neuroinflammation. Original research demonstrates that social hierarchy modulates methamphetamine reinforcement in rats and is associated with distinct phosphoproteomic signatures in the nucleus accumbens, with HDAC4 phosphorylation differing between dominant and subordinate rats. A mini-review discusses trace amine-associated receptors, particularly TAAR1, as potential therapeutic targets for anxiety and depression.