Li Xia, Cobb Charles E, May James M
Department of Medicine, Vanderbilt University School of Medicine, 715 Medical Research Building II, Nashville, TN 37232-6303, USA.
Arch Biochem Biophys. 2002 Jul 1;403(1):103-10. doi: 10.1016/S0003-9861(02)00205-9.
Mitochondria can regenerate ascorbic acid from its oxidized forms, which may help to maintain the vitamin both in mitochondria and in the cytoplasm. In this work, we sought to determine the site and mechanism of mitochondrial ascorbate recycling from dehydroascorbic acid. Rat skeletal muscle mitochondria incubated for 3 h at 37 degrees C with 500 microM dehydroascorbic acid and energy substrates maintained ascorbate concentrations more than twice those observed in the absence of substrate. Succinate-dependent mitochondrial reduction of dehydroascorbic acid was blocked by inhibitors of mitochondrial Complexes II and III. Neither cytochrome c nor the outer mitochondrial membrane were necessary for the effect. The ascorbate radical was generated by mitochondria during treatment with dehydroascorbic acid and was abolished by ferricyanide, which does not penetrate the mitochondrial inner membrane. Together, these results show that energy substrate-dependent ascorbate recycling from dehydroascorbic acid involves an externally exposed portion of mitochondrial complex III.
线粒体能够从其氧化形式再生抗坏血酸,这可能有助于在线粒体和细胞质中维持这种维生素。在这项研究中,我们试图确定线粒体从脱氢抗坏血酸中回收抗坏血酸的位点和机制。大鼠骨骼肌线粒体在37℃下与500微摩尔脱氢抗坏血酸和能量底物一起孵育3小时,所维持的抗坏血酸浓度是在无底物情况下观察到的浓度的两倍多。线粒体复合物II和III的抑制剂可阻断琥珀酸依赖性的线粒体对脱氢抗坏血酸的还原作用。细胞色素c和线粒体外膜对该作用均非必需。在用脱氢抗坏血酸处理期间,线粒体产生了抗坏血酸自由基,而铁氰化物可将其消除,铁氰化物无法穿透线粒体内膜。这些结果共同表明,能量底物依赖性的从脱氢抗坏血酸中回收抗坏血酸涉及线粒体复合物III的一个外部暴露部分。