Kitada M, Igarashi T, Kamataki T, Kitagawa H
Jpn J Pharmacol. 1977 Aug;27(4):481-9. doi: 10.1254/jjp.27.481.
There were marked differences among animal species between NADPH-dependent and ascorbic acid-Fe++-dependent lipid peroxidation. In NADPH-dependent lipid peroxidation, this activity occurred to the greatest extent in rats followed by guinea pigs and rabbits and such was much lower in rabbits than in guinea pigs. On the other hand, rabbit microsomes exhibited higher lipid peroxidation activity than guinea pigs in ascorbic acid plus Fe++ or Fe++-dependent lipid peroxidation although the activity was still lower than in rats. The ascorbic acid plus Fe++-stimulated lipid peroxidation produced a decrease in ethylmorphine N-demethylase activity which was closely related to ethylmorphine-enhanced NADPH-cytochrome P-450 reductase activity but was not related to the change of the apparent content of cytochrome P-450 in all animal species. These results indicate that decrease of NADPH-cytochrome P-450 reductase activity induces a decrease in ethylmorphine N-demethylase activity by lipid peroxidation.
在动物物种之间,NADPH依赖性脂质过氧化和抗坏血酸 - Fe++依赖性脂质过氧化存在显著差异。在NADPH依赖性脂质过氧化中,这种活性在大鼠中最为显著,其次是豚鼠和兔子,并且兔子中的活性远低于豚鼠。另一方面,在抗坏血酸加Fe++或Fe++依赖性脂质过氧化中,兔微粒体表现出比豚鼠更高的脂质过氧化活性,尽管该活性仍低于大鼠。抗坏血酸加Fe++刺激的脂质过氧化导致乙基吗啡N - 脱甲基酶活性降低,这与乙基吗啡增强的NADPH - 细胞色素P - 450还原酶活性密切相关,但与所有动物物种中细胞色素P - 450的表观含量变化无关。这些结果表明,NADPH - 细胞色素P - 450还原酶活性的降低通过脂质过氧化诱导乙基吗啡N - 脱甲基酶活性降低。