Aruoma O I, Halliwell B, Laughton M J, Quinlan G J, Gutteridge J M
Department of Biochemistry, University of London King's College, Strand, U.K.
Biochem J. 1989 Mar 1;258(2):617-20. doi: 10.1042/bj2580617.
When Fe2+ ions are added to rat-liver microsomes, lipid peroxidation begins after a short lag period. Fe2+-dependent peroxidation in the first few minutes of the incubation can be increased by adding Fe3+, ascorbic acid or Pb2+ ions; these stimulations are not additive. By contrast, Pb2+ ions inhibit peroxidation of microsomes in the presence of Fe3+/ascorbate or Fe3+-ADP/NADPH. In liposomes made from ox-brain phospholipids, Fe2+-dependent peroxidation is stimulated slightly by Fe3+, but much more so by ascorbic acid, Al3+ or Pb2+; these stimulations are not additive. Liposomal peroxidation in the presence of Fe3+/ascorbate is inhibited by Pb2+ or Al3+. These results argue against the participation of an Fe2+-Fe3+-O2 complex, or a critical 1:1 ratio of Fe2+ to Fe3+, in the initiation of lipid peroxidation in liposomes and rat-liver microsomes.
当向大鼠肝脏微粒体中添加Fe2+离子时,脂质过氧化在短暂的延迟期后开始。孵育最初几分钟内依赖Fe2+的过氧化反应可通过添加Fe3+、抗坏血酸或Pb2+离子而增强;这些刺激作用并非累加的。相比之下,在存在Fe3+/抗坏血酸盐或Fe3+-ADP/NADPH的情况下,Pb2+离子会抑制微粒体的过氧化反应。在用牛脑磷脂制成的脂质体中,Fe3+对依赖Fe2+的过氧化反应有轻微刺激作用,但抗坏血酸、Al3+或Pb2+的刺激作用更强;这些刺激作用并非累加的。在存在Fe3+/抗坏血酸盐的情况下,脂质体的过氧化反应会被Pb2+或Al3+抑制。这些结果表明,Fe2+-Fe3+-O2复合物或Fe2+与Fe3+的关键1:1比例并不参与脂质体和大鼠肝脏微粒体中脂质过氧化的起始过程。