Sedlak Thomas W, Saleh Masoumeh, Higginson Daniel S, Paul Bindu D, Juluri Krishna R, Snyder Solomon H
Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Proc Natl Acad Sci U S A. 2009 Mar 31;106(13):5171-6. doi: 10.1073/pnas.0813132106. Epub 2009 Mar 13.
Glutathione (GSH) and bilirubin are prominent endogenous antioxidant cytoprotectants. Despite tissue levels that are thousands of times lower than GSH, bilirubin is effective because of the biosynthetic cycle wherein it is generated from biliverdin by biliverdin reductase (BVR). When bilirubin acts as an antioxidant, it is oxidized to biliverdin, which is immediately reduced by BVR to bilirubin. Why does the body employ both of these 2 distinct antioxidant systems? We show that the water-soluble GSH primarily protects water soluble proteins, whereas the lipophilic bilirubin protects lipids from oxidation. Mice with deletion of heme oxygenase-2, which generates biliverdin, display greater lipid than protein oxidation, while the reverse holds for GSH depletion. RNA interference depletion of BVR increases oxidation of lipids more than protein. Depletion of BVR or GSH augments cell death in an oxidant-specific fashion.
谷胱甘肽(GSH)和胆红素是重要的内源性抗氧化细胞保护剂。尽管组织中的胆红素水平比谷胱甘肽低数千倍,但由于其生物合成循环,胆红素仍具有抗氧化作用,在该循环中,胆红素由胆绿素还原酶(BVR)从胆绿素生成。当胆红素作为抗氧化剂起作用时,它被氧化为胆绿素,而胆绿素会立即被BVR还原为胆红素。为什么身体会同时使用这两种不同的抗氧化系统呢?我们发现,水溶性的谷胱甘肽主要保护水溶性蛋白质,而亲脂性的胆红素则保护脂质免受氧化。缺乏生成胆绿素的血红素加氧酶-2的小鼠,脂质氧化比蛋白质氧化更严重,而谷胱甘肽耗竭的小鼠则相反。通过RNA干扰使BVR缺失,脂质氧化比蛋白质氧化增加得更多。BVR或谷胱甘肽的耗竭以氧化剂特异性方式增强细胞死亡。