Szabados G, Andó A, Tretter L, Horváth I
J Bioenerg Biomembr. 1987 Feb;19(1):21-30. doi: 10.1007/BF00769729.
Lipid peroxidation in isolated rat liver mitochondria, mitoplast, and mitochondrial inner membrane fragments was induced either by ferrous ions, or in an NADPH-dependent process by complexing with adenine nucleotides (ADP or ATP) iron. The Fe2+-induced lipid peroxidation is nonenzymic when inner membrane fragments are used, while the differences in the inhibitory effect of Mn2+ ions and the stimulatory effect of the ionophore A-23187 in mitochondria and inner membrane fragments suggest an enzymic mechanism for ferrous ion-induced lipid peroxidation in intact mitochondria. Contrary to this the ADP/Fe/NADPH-dependent lipid peroxidation is an enzymic process both in mitochondria and inner membrane preparations. We have shown that cytochrome P450 is involved in the ADP/Fe/NADPH-induced lipid peroxidation. Succinate, a known inhibitor of NADPH-dependent lipid peroxidation, inhibited the Fe2+-induced process also, and there was no difference in this effect when inner membrane preparations, mitochondria, or mitoplasts were used.
在分离的大鼠肝线粒体、线粒体膜间腔和线粒体内膜片段中,脂质过氧化作用可由亚铁离子诱导产生,或者在一个依赖于NADPH的过程中,通过与腺嘌呤核苷酸(ADP或ATP)形成络合物的铁来诱导产生。当使用内膜片段时,Fe2+诱导的脂质过氧化是非酶促的,而线粒体和内膜片段中Mn2+离子的抑制作用以及离子载体A-23187的刺激作用的差异表明,完整线粒体中亚铁离子诱导的脂质过氧化存在酶促机制。与此相反,ADP/Fe/NADPH依赖的脂质过氧化在线粒体和内膜制剂中都是酶促过程。我们已经表明细胞色素P450参与了ADP/Fe/NADPH诱导的脂质过氧化。琥珀酸是一种已知的NADPH依赖的脂质过氧化抑制剂,它也抑制Fe2+诱导的过程,并且当使用内膜制剂、线粒体或线粒体膜间腔时,这种作用没有差异。