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哺乳动物CYP3A诱导剂对草鱼(Ctenopharyngodon idellus)中CYP3A相关酶活性的影响:对建立鱼类CYP3A诱导模型的潜在意义。

Effects of mammalian CYP3A inducers on CYP3A-related enzyme activities in grass carp (Ctenopharyngodon idellus): Possible implications for the establishment of a fish CYP3A induction model.

作者信息

Li Dan, Yang Xian-Le, Zhang Shu-Jun, Lin Mao, Yu Wen-Juan, Hu Kun

机构信息

Aquatic Pathogen Collection Centre of Ministry of Agriculture, Shanghai Fisheries University, 334 Jungong Road, Shanghai 200090, China.

出版信息

Comp Biochem Physiol C Toxicol Pharmacol. 2008 Jan;147(1):17-29. doi: 10.1016/j.cbpc.2007.07.003. Epub 2007 Jul 21.

Abstract

Unexpected drug-drug interactions in fish are generally associated with the induction of CYP3A activity and may lead to the formation of drug residues and thus threaten the safety of fishery products. However, little information is available about CYP3A induction in fish. In the present study, we determined the in vivo and in vitro effects of typical mammalian CYP3A inducers (rifampicin, phenobarbital and dexamethasone) on CYP3A-related enzyme activities in a freshwater teleost, the grass carp (Ctenopharyngodon idellus). Our results showed that the response to rifampicin was similar for grass carp liver cell line (GCL), liver microsomes and the primary hepatocytes of grass carp, as indicated by the activity of aminopyrine N-demethylase (APND). When erythromycin N-demethylase (ERND) and 6beta-testosterone hydroxylase (6beta-TOH) were taken into consideration, the GCL displayed a greater capacity for conducting CYP3A metabolism and induction than the C. idellus kidney cell line (CIK). Using erythromycin and testosterone as substrates, we demonstrated that CYP3A catalysis exhibited non-Michaelis-Menten kinetics in GCL cells, and that V(max)/K(m) values were significantly increased due to rifampicin-treatment. Overall, this study may have implications for the use of GCL as a CYP3A induction model to identify physiological changes in fish as well as the similarities or differences between fish and mammals.

摘要

鱼类中意外的药物相互作用通常与细胞色素P450 3A(CYP3A)活性的诱导有关,可能导致药物残留的形成,从而威胁到渔业产品的安全。然而,关于鱼类中CYP3A诱导的信息很少。在本研究中,我们测定了典型的哺乳动物CYP3A诱导剂(利福平、苯巴比妥和地塞米松)对淡水硬骨鱼草鱼(Ctenopharyngodon idellus)体内和体外CYP3A相关酶活性的影响。我们的结果表明,草鱼肝细胞系(GCL)、肝微粒体和草鱼原代肝细胞对利福平的反应相似,以氨基比林N-脱甲基酶(APND)的活性为指标。当考虑红霉素N-脱甲基酶(ERND)和6β-睾酮羟化酶(6β-TOH)时,GCL显示出比草鱼肾细胞系(CIK)更强的进行CYP3A代谢和诱导的能力。以红霉素和睾酮为底物,我们证明CYP3A催化在GCL细胞中表现出非米氏动力学,并且由于利福平处理,V(max)/K(m)值显著增加。总体而言,本研究可能对将GCL用作CYP3A诱导模型以识别鱼类的生理变化以及鱼类与哺乳动物之间的异同具有启示意义。

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