Kawamoto T, Hobara T, Nakamura K, Imamura A, Ogino K, Kobayashi H, Iwamoto S, Sakai T
Department of Public Health, Yamaguchi University School of Medicine, Ube, Japan.
Toxicology. 1988 Dec 30;53(2-3):239-49. doi: 10.1016/0300-483x(88)90217-x.
Several reports have described the effects of trichloroethylene (TCE) on the microsomal mixed function oxidase system (MFOS). These studies suggest that repeated TCE administration induces MFOS, especially cytochrome P-450 and NADPH-cytochrome c reductase. However, it is uncertain what isozymes are induced by TCE treatment, and it is not clear how microsomal enzymes or cytochrome P-450 isozymes are altered when TCE is administered for a duration longer than 28 days. We investigated the changes of MFOS by long-term TCE treatment. Male Wistar rats were injected with TCE, 1.0 g/kg body weight once a day for 5 continuous days or 2.0 g/kg body weight twice a week for 15 days. The mean body weight of the rats treated with TCE for 15 weeks was slightly, but not significantly, less than that of the control rats. Relative liver weights (liver wt/body wt) of the TCE-treated group were however significantly larger (21%) than those of the control group. The weights of the other organs were not changed by long-term TCE treatment. Trichloroethylene treatments for 5 days and 15 weeks caused significant increases in microsomal protein, cytochrome P-450, cytochrome b-5 and NADPH-cytochrome c reductase. TCE treatments produced an increase in a polypeptide band at 52,000 molecular weight range observed with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). This increase in similar to, but less pronounced than that induced by phenobarbital (PB) treatment. There were no remarkable changes at 56,000 molecular weight range where a band appeared after the treatment with 3-methylcholanthrene (MC). It is likely that the induction of cytochrome P-450 by TCE is relatively similar to that by PB.
有几份报告描述了三氯乙烯(TCE)对微粒体混合功能氧化酶系统(MFOS)的影响。这些研究表明,反复给予TCE可诱导MFOS,尤其是细胞色素P-450和NADPH-细胞色素c还原酶。然而,尚不确定TCE处理诱导的是哪些同工酶,并且当TCE给药时间超过28天时微粒体酶或细胞色素P-450同工酶如何改变也不清楚。我们研究了长期TCE处理对MFOS的影响。雄性Wistar大鼠每天注射1.0 g/kg体重的TCE,连续5天,或每周两次注射2.0 g/kg体重的TCE,共15天。经TCE处理15周的大鼠平均体重略低于对照组,但差异不显著。然而,TCE处理组的相对肝脏重量(肝脏重量/体重)比对照组显著大(21%)。长期TCE处理未改变其他器官的重量。TCE处理5天和15周导致微粒体蛋白、细胞色素P-450、细胞色素b-5和NADPH-细胞色素c还原酶显著增加。TCE处理使十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)观察到的分子量在52,000范围内的一条多肽带增加。这种增加与苯巴比妥(PB)处理诱导的增加相似,但不太明显。在用3-甲基胆蒽(MC)处理后出现条带的56,000分子量范围内没有显著变化。TCE对细胞色素P-450的诱导可能与PB相对相似。