Borthiry Griselda R, Antholine William E, Kalyanaraman B, Myers Judith M, Myers Charles R
Department of Pharmacology and Toxicology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.
Free Radic Biol Med. 2007 Mar 15;42(6):738-55; discussion 735-7. doi: 10.1016/j.freeradbiomed.2006.10.055. Epub 2006 Dec 15.
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 b(5) and NADPH:P450 reductase. Under aerobic conditions, the PLs reduced Cr(VI) to Cr(V) which was confirmed by ESR using isotopically pure (53)Cr(VI). When 5-diethoxyphosphoryl-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 (O(2)(-)) adduct. These adducts were observed even at very low Cr(VI) concentrations (10 muM). NADPH, Cr(VI), O(2), and the PLs were all required for significant HO() generation. Superoxide dismutase eliminated the O(2)(-) adduct and resulted in a 30% increase in the HO() adduct. Catalase largely diminished the HO() adduct signal, indicating its dependence on H(2)O(2). 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 H(2)O(2) was not needed, indicating that it was generated by the PLs. Adding exogenous H(2)O(2), however, did increase the amount of DEPMPO/HO() adduct. The inclusion of formate yielded the carbon dioxide radical adduct of DEPMPO, and experiments with dimethyl sulfoxide (DMSO) plus the spin trap alpha-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 b(5) in the generation of HO(). Overall, the simultaneous generation of Cr(V) and H(2)O(2) by the PLs and the resulting generation of HO() at low Cr(VI) concentrations could have important implications for Cr(VI) toxicity.
六价铬(Cr(VI))的还原可产生活性铬中间体和各种类型的氧化应激。使用含有纯化细胞色素b(5)和NADPH:P450还原酶的重组蛋白脂质体(PLs)研究了人微粒体酶在自由基生成中的潜在作用。在有氧条件下,PLs将Cr(VI)还原为Cr(V),这通过使用同位素纯的(53)Cr(VI)的电子顺磁共振(ESR)得到证实。当加入5-二乙氧基磷酰基-5-甲基-1-吡咯啉-N-氧化物(DEPMPO)作为自旋捕获剂时,观察到了非常明显的羟基自由基(HO·)加合物信号以及较小的超氧阴离子(O₂⁻)加合物信号。即使在非常低的Cr(VI)浓度(10 μM)下也能观察到这些加合物。显著的HO·生成需要NADPH、Cr(VI)、O₂和PLs。超氧化物歧化酶消除了O₂⁻加合物,并使HO·加合物增加了30%。过氧化氢酶大大减弱了HO·加合物信号,表明其对H₂O₂的依赖性。发现一些过氧化氢酶来源含有可混淆结果的Cr(VI)还原污染物,但本研究使用了不含这些污染物的过氧化氢酶来源。不需要外源H₂O₂,表明它是由PLs产生的。然而,添加外源H₂O₂确实增加了DEPMPO/HO·加合物的量。加入甲酸盐产生了DEPMPO的二氧化碳自由基加合物,用二甲基亚砜(DMSO)加自旋捕获剂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·的生成。随着时间对各种物质的定量分析与相对于还原的Cr(VI)净量而言HO·的化学计量过量一致。这也首次证明了细胞色素b(5)在HO·生成中的作用。总体而言,PLs同时生成Cr(V)和H₂O₂以及在低Cr(VI)浓度下由此产生的HO·可能对Cr(VI)毒性具有重要意义。