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Reduction of Hexavalent Chromium by Human Cytochrome b5: Generation of Hydroxyl Radical and Superoxide

机译:人类细胞色素b5还原六价铬:生成羟基自由基和超氧化物

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摘要

The reduction of hexavalent chromium, Cr(VI), can generate reactive Cr intermediates and various types of oxidative stress. The potential role of human microsomal enzymes in free radical generation was examined using reconstituted proteoliposomes (PLs) containing purified cytochrome b5 and NADPH:P450 reductase. Under aerobic conditions, the PLs reduced Cr(VI) to Cr(V) which was confirmed by ESR using isotopically pure 53Cr(VI). When 5-Diethoxyphos-phoryl-5-methyl-1-pyrroline-N-oxide (DEPMPO) was included as a spin trap, a very prominent signal for the hydroxyl radical (HO) adduct was observed as well as a smaller signal for the superoxide (O2•−) adduct. These adducts were observed even at very low Cr(VI) concentrations (10 μM). NADPH, Cr(VI), O2 and the PLs were all required for significant HO generation. Superoxide dismutase eliminated the O2• − adduct and resulted in a 30% increase in the HO adduct. Catalase largely diminished the HO adduct signal indicating its dependence on H2O2. Some sources of catalase were found to have Cr(VI)-reducing contaminants which could confound results, but a source of catalase free of these contaminants was used for these studies. Exogenous H2O2 was not needed, indicating that it was generated by the PLs. Adding exogenous H2O2, however, did increase the amount of DEPMPO/HO adduct. The inclusion of formate yielded the carbon dioxide radical adduct of DEPMPO, and experiments with dimethylsulfoxide (DMSO) plus the spin trap α-phenyl-N-tert-butylnitrone (PBN) yielded the methoxy and methyl radical adducts of PBN, confirming the generation of HO. Quantification of the various species over time was consistent with a stoichiometric excess of HO relative to the net amount of Cr(VI) reduced. This also represents the first demonstration of a role for cytochrome b5 in the generation of HO. Overall, the simultaneous generation of Cr(V) and H2O2 by the PLs and the resulting generation of HO at low Cr(VI) concentrations could have important implications for Cr(VI) toxicity.
机译:六价铬Cr(VI)的还原可生成活性Cr中间体和各种类型的氧化应力。使用包含纯化的细胞色素b5和NADPH:P450还原酶的重组蛋白脂质体(PLs),检查了人类微粒体酶在自由基产生中的潜在作用。在好氧条件下,PLs将Cr(VI)还原为Cr(V),这是通过ESR使用同位素纯 53 Cr(VI)证实的。当包含5-二乙氧基磷酰基--5-甲基-1-吡咯啉-N-氧化物(DEPMPO)作为自旋阱时,观察到非常明显的羟基自由基(HO )加合物信号以及超氧化物(O2 •-)加合物的较小信号。即使在极低的Cr(VI)浓度(10μM)下也观察到了这些加合物。 NADPH,Cr(VI),O2和PL都是产生大量HO 所必需的。超氧化物歧化酶消除了O2 •-加合物,并使HO 加合物增加了30%。过氧化氢酶大大减少了HO 加合物信号,表明其对H2O2的依赖性。发现过氧化氢酶的某些来源具有降低Cr(VI)的污染物,可能会混淆结果,但是将不含这些污染物的过氧化氢酶来源用于这些研究。不需要外源的H2O2,表明它是由PL生成的。但是,添加外源H2O2确实增加了DEPMPO / HO 加合物的量。甲酸的加入产生了DEPMPO的二氧化碳自由基加合物,用二甲基亚砜(DMSO)加上自旋阱α-苯基-N-叔丁基硝酮(PBN)进行的实验产生了PBN的甲氧基和甲基自由基加合物,证实了HO 。随着时间的推移,各种物种的定量与HO 相对于还原的Cr(VI)净量的化学计量过量是一致的。这也首次证明了细胞色素b5在HO 的产生中的作用。总体而言,PLs同时生成Cr(V)和H2O2以及在低Cr(VI)浓度下生成HO 可能对Cr(VI)毒性具有重要意义。

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