Biro-Sauveur B, Eeckhoutte C, Baeza E, Boulard C, Galtier P
Laboratoire de Pharmacologie-Toxicologie INRA, Toulouse, France.
Int J Parasitol. 1995 Oct;25(10):1193-200. doi: 10.1016/0020-7519(95)00035-z.
The activity of drug-metabolizing enzymes was compared in liver, kidneys and lungs of rats given single or repetitive fluke infections. Fascioliasis was induced by oral administration of 20 metacercariae of F. hepatica to rats, either 6, or 12 and 6, or 12, 9 and 6 weeks before sacrifice. In the liver of mono-infected rats, significant reductions (24-67%) were observed in microsomal content of cytochrome P450 and all P450-dependent monooxygenases investigated. Conjugations to glutathione or acetate were lowered by 34-50% in these animals. In multiply infected animals, a majority of specific enzymatic activities were unchanged, while some monooxygenase activities such as aminopyrine demethylation or benzo(a)pyrene hydroxylation were increased by 26-76% in the liver of tri-infected rats. A renal compensatory process occurred in all infected groups, since cytochrome P450, benzphetamine demethylation and glutathione conjugation were significantly increased. By contrast, dealkylation of benzphetamine and pentoxyresorufin were decreased in the lungs of monoinfected rats. The development of parasite resistance would account for the recovery of liver drug metabolizing capabilities in multi-infected animals.
在单次或反复感染吸虫的大鼠的肝脏、肾脏和肺中比较了药物代谢酶的活性。通过在处死前6周、或12周和6周、或12周、9周和6周给大鼠口服20个肝片形吸虫囊蚴来诱发肝片吸虫病。在单次感染大鼠的肝脏中,观察到细胞色素P450的微粒体含量以及所研究的所有P450依赖性单加氧酶均显著降低(24%-67%)。这些动物中与谷胱甘肽或乙酸盐的结合降低了34%-50%。在多次感染的动物中,大多数特异性酶活性未发生变化,而在三重感染大鼠的肝脏中,一些单加氧酶活性如氨基比林去甲基化或苯并(a)芘羟基化增加了26%-76%。所有感染组均出现肾脏代偿过程,因为细胞色素P450、苄非他明去甲基化和谷胱甘肽结合均显著增加。相比之下,单次感染大鼠肺中苄非他明和戊氧基试卤灵的脱烷基作用降低。寄生虫抗性的发展可以解释多次感染动物肝脏药物代谢能力的恢复。