Hardej D, Trombetta L D
College of Pharmacy and Allied Health Professions, St. John's University, Toxicology Program, 8000 Utopia Parkway, Jamaica, NY 11439, USA.
Toxicol Lett. 2002 May 28;131(3):215-26. doi: 10.1016/s0378-4274(02)00056-5.
Ebselen is a seleno-organic compound with documented cytoprotective properties. Little work has been done, however, demonstrating ebselen's cytoprotective properties in neural cell lines. In order to examine the effects of this compound and its mechanism of action, astrocytes were exposed to two known neurotoxicants, cisplatin and diethyldithiocarbamate (DDC). Cells were pretreated with 30 microM ebselen and subsequently treated with either 150 microM DDC for 1 h or 250 and 500 microM cisplatin for 24 h. Results indicate significant increases in viability in cells pretreated with ebselen and exposed to cisplatin. Ebselen pretreatment did not significantly increase viability in cells exposed to DDC. Light and scanning electron microscopy studies confirm the viability studies. Gross morphological damage was seen in cells treated with cisplatin, however, cells pretreated with ebselen and then exposed to cisplatin, appeared similar to controls. No differences were noted in cells pretreated with ebselen and then exposed to DDC or cells treated with DDC alone. In order to examine the mechanism of protection of this compound, glutathione status was examined. Results show that ebselen does not significantly increase reduced or oxidized glutathione (GSH, GSSG). All cell groups treated with cisplatin showed an increase in GSH levels. Ebselen showed protection in glutathione depleted cells at the 250 microM cisplatin dose. DDC treatment showed no significant increase in either reduced or oxidized glutathione. We conclude that ebselen significantly protects against cisplatin, but not DDC toxicity. We further conclude that this protection is not related to changes in glutathione status in the rat hippocampal cell line as has been reported in other cell types.
依布硒啉是一种具有细胞保护特性记录的有机硒化合物。然而,关于依布硒啉在神经细胞系中的细胞保护特性的研究较少。为了研究该化合物的作用效果及其作用机制,将星形胶质细胞暴露于两种已知的神经毒素顺铂和二乙基二硫代氨基甲酸盐(DDC)中。细胞先用30微摩尔/升的依布硒啉预处理,随后用150微摩尔/升的DDC处理1小时或用250和500微摩尔/升的顺铂处理24小时。结果表明,用依布硒啉预处理并暴露于顺铂的细胞活力显著增加。依布硒啉预处理并未显著提高暴露于DDC的细胞的活力。光学和扫描电子显微镜研究证实了活力研究结果。在用顺铂处理的细胞中可见明显的形态损伤,然而,先用依布硒啉预处理然后暴露于顺铂的细胞,其外观与对照相似。在用依布硒啉预处理然后暴露于DDC的细胞或单独用DDC处理的细胞中未观察到差异。为了研究该化合物的保护机制,检测了谷胱甘肽状态。结果显示,依布硒啉并未显著增加还原型或氧化型谷胱甘肽(GSH、GSSG)的水平。所有用顺铂处理的细胞组的GSH水平均升高。在250微摩尔/升顺铂剂量下,依布硒啉对谷胱甘肽耗竭的细胞具有保护作用。DDC处理并未使还原型或氧化型谷胱甘肽显著增加。我们得出结论,依布硒啉能显著保护细胞免受顺铂的毒性作用,但不能保护细胞免受DDC的毒性作用。我们进一步得出结论,这种保护作用与大鼠海马细胞系中谷胱甘肽状态的变化无关,而其他细胞类型中曾有相关报道。