Ramsay R R, Singer T P
Molecular Biology Division, Veterans Affairs Medical Center, San Francisco, CA 94121.
Biochem Biophys Res Commun. 1992 Nov 30;189(1):47-52. doi: 10.1016/0006-291x(92)91523-s.
The addition of NADH to submitochondrial particles inhibited by agents which interrupt electron transport from NADH-Q oxidoreductase (Complex I) to Q10 (rotenone, piericidin A, and MPP+) results in superoxide formation and lipid peroxidation. A study of the quantitative relations now shows that oxyradical formation does not appear to be the direct result of the inhibition. Although tetraphenyl boron (TPB) greatly enhances the inhibition by MPP+, it has no effect on O2. formation or lipid peroxidation. When submitochondrial particles completely inhibited by rotenone or piericidin A are treated with bovine serum albumin to remove spuriously bound inhibitor molecules without affecting those bound at the specific inhibition site, NADH-Q activity remains inhibited and lipid peroxidation occurs but superoxide formation ceases. Thus oxyradical formation may be the result of the binding of inhibitors at sites in the membrane other than those related to the inhibition of electron transport.
向被能中断从NADH-Q氧化还原酶(复合体I)到辅酶Q10的电子传递的试剂(鱼藤酮、杀粉蝶菌素A和MPP+)抑制的亚线粒体颗粒中添加NADH会导致超氧化物的形成和脂质过氧化。一项关于定量关系的研究现在表明,氧自由基的形成似乎不是抑制作用的直接结果。尽管四苯基硼(TPB)极大地增强了MPP+的抑制作用,但它对超氧阴离子的形成或脂质过氧化没有影响。当用鱼藤酮或杀粉蝶菌素A完全抑制的亚线粒体颗粒用牛血清白蛋白处理以去除虚假结合的抑制剂分子而不影响在特异性抑制位点结合的分子时,NADH-Q活性仍然受到抑制且脂质过氧化发生,但超氧化物的形成停止。因此,氧自由基的形成可能是抑制剂在膜上与抑制电子传递无关的位点结合的结果。