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Neurotoxicity research

ISSN 1476-3524

2 papers in the library · 3 citations · publishing 2016-2025

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.

Are Alcohol Anti-relapsing and Alcohol Withdrawal Drugs Useful in Cannabinoid Users?

Neurotoxicity research November 1, 2016 Patrycja Kleczkowska, Irena Smaga, Malgorzata Filip et al.

Cannabinoids, despite their illegal status, have recognized therapeutic potential and are often used recreationally by young adults, sometimes as an alternative to other drugs or to enhance pleasure. They are frequently taken alongside medications for alcohol use disorder (AUD) and alcohol withdrawal syndrome (AWS), such as disulfiram, acamprosate, and naltrexone. This paper reviews recent findings on possible beneficial effects and interactions between cannabinoids and these AUD/AWS medications, whether the conditions are comorbid or separate.