1. Selected ebselen analogs reduce mechlorethamine toxicity in vitro.
- Author
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Pino MA, Pietka-Ottlik M, and Billack B
- Subjects
- Antioxidants chemistry, Azoles chemistry, Cell Line, Tumor, Cell Survival drug effects, Humans, Isoindoles, Lipid Peroxidation drug effects, Malondialdehyde metabolism, Microscopy, Phase-Contrast, Molecular Structure, Organoselenium Compounds chemistry, Skin metabolism, Skin pathology, Structure-Activity Relationship, Antioxidants pharmacology, Azoles pharmacology, Mechlorethamine toxicity, Mustard Gas toxicity, Organoselenium Compounds pharmacology, Skin drug effects
- Abstract
Sulfur mustard (SM) is a potent vesicant. The lack of an effective antidote makes SM a continued threat to both military and civilian settings. A surrogate agent, namely mechlorethamine (HN2), was used here to mimic the toxicity of SM, and the main objective of this study was to demonstrate if selected organoselenium analogs could protect cultured A-431 skin cells from HN2 toxicity. Test compounds included ebselen (EB-1) and three related organoselenium analogs (EB-2, EB-3 and EB-4). In the absence of test compound, a reproducible and robust cell death was observed in the cells following incubation with HN2 (25 µM, 24 or 48 h) while cells treated with test compound alone (15, 30 or 60 µM) for similar periods of time were generally not affected. When incubated in the presence of both HN2 and test compound for 24 or 48 h, it was found that EB-1, EB-2, EB-3 and EB-4 could spare the cells from death, with the EB-4 compound being the most effective at reducing HN2 toxicity. Light microscopy confirmed these findings. The organoseleniums were also examined for their effects on reducing lipid peroxidation in the A-431 skin cells. Among the test compounds, EB-4 reduced lipid peroxidation by HN2 to the greatest extent. These studies, taken together, validate that the organoselenium antioxidants tested here may serve a purpose in the discovery of medical countermeasures to vesicants.
- Published
- 2014
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