Kawai K, Shiojiri H, Nakamaru T, Nozawa Y, Sugie S, Mori H, Kato T, Ogihara Y
Department of Biochemistry, Gifu University School of Medicine, Japan.
Cell Biol Toxicol. 1985 Jan;1(2):1-10. doi: 10.1007/BF00717786.
The duclauxin derivatives xenoclauxin and desacetylduclauxin were examined for their effects on the growth of L-1210 murine leukemia cells, on the induction of DNA repair in the rat and mouse hepatocyte primary culture (HPC/DNA repair test), and on oxidative phosphorylation in mitochondria from rat livers in comparison to duclauxin. Both derivatives inhibited the growth of L-1210 culture cells as strongly as duclauxin. Duclauxin derivatives were negative in the HPC/DNA repair test. Xenoclauxin exhibited a potent uncoupling effect accompanying a marked depression of state 3 respiration of mitochondria in a similar fashion to that of duclauxin. Desacetylduclauxin significantly inhibited the state 3 respiration without causing uncoupling of oxidative phosphorylation in mitochondria. These results strongly suggest that xenoclauxin and desacetylduclauxin from Penicillium duclauxii are not genotoxic but are cytotoxic mainly due to their potent inhibition of ATP synthesis in mitochondria.
检测了杜克洛辛衍生物异杜克洛辛和去乙酰杜克洛辛对L - 1210小鼠白血病细胞生长的影响、对大鼠和小鼠肝细胞原代培养物中DNA修复的诱导作用(HPC/DNA修复试验)以及与杜克洛辛相比对大鼠肝脏线粒体氧化磷酸化的影响。两种衍生物对L - 1210培养细胞生长的抑制作用与杜克洛辛一样强烈。杜克洛辛衍生物在HPC/DNA修复试验中呈阴性。异杜克洛辛表现出强大的解偶联作用,同时线粒体状态3呼吸显著降低,其方式与杜克洛辛相似。去乙酰杜克洛辛显著抑制状态3呼吸,而不引起线粒体氧化磷酸化解偶联。这些结果有力地表明,来自杜氏青霉的异杜克洛辛和去乙酰杜克洛辛没有遗传毒性,但具有细胞毒性,主要是因为它们对线粒体ATP合成有强大的抑制作用。