Protective effects of tiopronin on oxidatively challenged human lung carcinoma cells (A549)

被引:5
作者
Beltz, Justin [1 ]
Chernatynskaya, Anna [1 ]
Pfaff, Annalise [1 ]
Ercal, Nuran [1 ]
机构
[1] Missouri Univ Sci & Technol, Dept Chem, 230 Schrenk Hall,400 W 11th St, Rolla, MO 65409 USA
基金
美国国家卫生研究院;
关键词
Thiols; antioxidant; oxidative stress; reactive oxygen species; glutathione; tiopronin; TERT-BUTYL HYDROPEROXIDE; HYDROGEN-PEROXIDE; INDUCED CATARACT; D-PENICILLAMINE; ANTIOXIDANT; 2-MERCAPTOPROPIONYLGLYCINE; PHARMACOKINETICS; SEQUESTRATION; DELIVERY; CYSTEINE;
D O I
10.1080/10715762.2020.1763332
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tiopronin (MPG) is a thiol antioxidant drug that has been explored as a treatment for various oxidative stress-related disorders. However, many of its antioxidant capabilities remain untested in well-validated cell models. To more thoroughly understand the action of this promising pharmaceutical compound against acute oxidative challenge, A549 human lung carcinoma cells were exposed totert-butyl hydroperoxide (tBHP) and treated with MPG. Analyses of cell viability, intracellular glutathione (GSH) levels, and the prevalence of reactive oxygen species (ROS) and mitochondrial superoxide were used to examine the effects of MPG ontBHP-challenged cells. MPG treatment suppressed intracellular ROS and mitochondrial superoxide and preventedtBHP-induced GSH depletion and apoptosis. These results indicate that MPG is effective at preserving redox homeostasis against acute oxidative insult in A549 cells if present at sufficient concentrations during exposure to oxidants such astBHP. The effects of treatment gleaned from this study can inform experimental design for futurein vivowork on the therapeutic potential of MPG.
引用
收藏
页码:319 / 329
页数:11
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