Tert-butylhydroperoxide bioactivation to methyl radical in rat liver mitochondria and submitochondrial particles.

A Iannone, A Bini, Y G Jin, V Vannini, A Tomasi
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引用次数: 7

Abstract

Electron paramagnetic resonance spectroscopy (EPR) coupled to the spin trapping technique was used to detect carbon-centered radicals in rat liver mitochondria and submitochondrial particles exposed to t-butyl-hydroperoxide (TBH), using the spin trapping agent 3,5-dibromo-4-nitroso-benzenesulfonic acid (DBNBS). The signal recorded was unambiguously assigned to the methyl radical adduct. DBNBS was added to isolated rat liver mitochondria energized with succinate, and the methyl radical adduct was observed. The addition of NADH, NADPH, inhibitors of the respiratory chain, and of monoaminoxidase (MAO) inhibitors did not cause any relevant modification in the yield of radical adduct formation. Boiling and the addition of a non-ionic detergent inhibited the formation of the radical adduct, while experiments carried out under hypoxic conditions generated a significant increase in methyl radical formation. Further experiments were carried out on sub-mitochondrial particles (SMP) giving rise to, basically, the same results. From the above results, we are proposing that haem prosthetic groups are the likely source of TBH bioactivation in mitochondria.

叔丁基过氧化氢对大鼠肝脏线粒体和亚线粒体颗粒甲基自由基的生物活性。
采用自旋捕获剂3,5-二溴-4-亚硝基苯磺酸(DBNBS),利用电子顺磁共振波谱(EPR)和自旋捕获技术检测暴露于t-丁基氢过氧化物(TBH)的大鼠肝脏线粒体和亚线粒体颗粒中的碳中心自由基。所记录的信号被明确地分配给甲基自由基加合物。将DBNBS加入琥珀酸激活的离体大鼠肝脏线粒体中,观察甲基自由基加合物的变化。煮沸和加入非离子洗涤剂抑制了自由基加合物的形成,而在缺氧条件下进行的实验则显著增加了甲基自由基的形成。在亚线粒体颗粒(SMP)上进行了进一步的实验,基本上得到了相同的结果。根据上述结果,我们提出血红素假基可能是线粒体中TBH生物激活的来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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