Hodgson P D, Renton K W
Department of Pharmacology, Dalhousie University, Halifax, Nova Scotia, Canada.
Int J Immunopharmacol. 1995 Dec;17(12):995-1000. doi: 10.1016/0192-0561(95)00083-6.
The down-regulation of cytochrome P450 during host defence involves one or more mediators of unknown source and identity. Owing to striking similarities in the features that are involved in the production of NO and the features involved in the down-regulation of cytochrome P450 we hypothesized that NO could be a mediator in the interferon-evoked loss of cytochrome P450. In these experiments the nitric oxide synthase inhibitor L-nitroarginine (5 mg/kg) failed to protect mice from the down-regulation of cytochrome P450, ethoxyresorufin dealkylase and para-nitrophenol hydroxylase in the liver following administration of the interferon inducer polyinosinic.polycytidylic acid. A higher dose of L-nitroarginine (30 mg/kg) given every 12 h for 3 days also did not protect against cytochrome P450 losses. In addition, no down-regulation of the enzyme was observed in animals treated with multiple doses of the NO-generating drugs glyceryl trinitrate (16 and 80 mg/kg given every 4 h for 16 h) and nitroprusside (20 and 100 mg/kg given every 4 h for 16 h). These results indicate that the down-regulation of cytochrome P450 by interferon or its inducers probably does not involve NO as a required intermediary.
宿主防御过程中细胞色素P450的下调涉及一种或多种来源和性质不明的介质。由于一氧化氮(NO)产生过程中涉及的特征与细胞色素P450下调过程中涉及的特征存在显著相似性,我们推测NO可能是干扰素诱发的细胞色素P450缺失的介质。在这些实验中,一氧化氮合酶抑制剂L-硝基精氨酸(5毫克/千克)未能保护小鼠免受干扰素诱导剂多聚肌苷酸-聚胞苷酸给药后肝脏中细胞色素P450、乙氧异吩唑酮脱烷基酶和对硝基苯酚羟化酶下调的影响。每12小时给予一次更高剂量的L-硝基精氨酸(30毫克/千克),持续3天,也不能防止细胞色素P450的损失。此外,在用多剂量的NO生成药物硝酸甘油(每4小时给予16毫克/千克和80毫克/千克,持续16小时)和硝普钠(每4小时给予20毫克/千克和100毫克/千克,持续16小时)处理的动物中,未观察到该酶的下调。这些结果表明,干扰素或其诱导剂对细胞色素P450的下调可能不涉及NO作为必需的中间介质。