Bilirubin and glutathione have complementary antioxidant and cytoprotective roles

被引:464
作者
Sedlak, Thomas W. [1 ,2 ]
Saleh, Masoumeh [2 ]
Higginson, Daniel S. [2 ]
Paul, Bindu D. [2 ]
Juluri, Krishna R. [2 ]
Snyder, Solomon H. [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
关键词
apoptosis; biliverdin; cell death; heme oxygenase; neuroprotection; HUMAN BILIVERDIN REDUCTASE; HEME OXYGENASE-2 PROTECTS; OXIDATIVE STRESS; SERUM BILIRUBIN; CARBON-MONOXIDE; BIOLOGICAL SAMPLES; METAANALYSIS; DISEASE; INJURY; SUPPLEMENTATION;
D O I
10.1073/pnas.0813132106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
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.
引用
收藏
页码:5171 / 5176
页数:6
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