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Inhibitory Effects of Calf Thymus DNA on Metabolism Activity of CYP450 Enzyme in Human Liver Microsomes

机译:小牛胸腺DNA对人肝微粒体CYP450酶代谢活性的抑制作用

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The present study investigated the effect of calf thymus DNA (ctDNA) on human hepatic cytochrome P450s (CYP450s) in vitro. Specific substrate probes for each isoform, CYP1A2, 2C9, 2C19, 2D6 and 3A4, were incubated using pooled human liver microsomes with or without ctDNA, and liquid chromatography coupled tandem mass spectrometry (LC-MS/MS) method was developed for the analysis of probe metabolites. Enzyme kinetics parameters K-i and IC50 values were estimated to determine the types and strength of inhibition. ctDNA could specifically inhibit the metabolism of CYP2C9 probe substrates, with the IC50 = 0.9955 mu g/ml, while it was not able to inhibit CYP1A2, CYP2C19, CYP2D6 or CYP3A4 (IC50 > 100 pg/ml). The results showed that ctDNA was a potent inhibitor of CYP2C9 enzyme, and has the metabolic interaction potential with the model drugs which are metabolism substrates of CYP2C9. The inhibition mechanism study suggested ctDNA may inhibit CYP2C9 by decreasing the activity of CYP450 reductase. These findings indicated that when the medical agents catalyzed mainly by CYP2C9 were co-administered in vivo with adsorptive material in vitro, the potential inhibitory effect of ctDNA on enzyme activity and the following metabolism character changes of the former should be highly focused on.
机译:本研究调查了小牛胸腺DNA(ctDNA)对人肝细胞色素P450(CYP450s)的影响。使用合并或不合并ctDNA的人肝微粒体孵育每种同工酶CYP1A2、2C9、2C19、2D6和3A4的特异性底物探针,并开发了液相色谱-串联质谱(LC-MS / MS)方法来分析探测代谢产物。估计酶动力学参数K-1和IC50值以确定抑制的类型和强度。 ctDNA可以特异性抑制CYP2C9探针底物的代谢,IC50 = 0.9955μg / ml,而不能抑制CYP1A2,CYP2C19,CYP2D6或CYP3A4(IC50> 100 pg / ml)。结果表明,ctDNA是一种有效的CYP2C9酶抑制剂,与作为CYP2C9代谢底物的模型药物具有代谢相互作用的潜力。抑制机制研究表明ctDNA可能通过降低CYP450还原酶的活性来抑制CYP2C9。这些发现表明,当以CYP2C9为主要催化活性的药物在体外与吸附性材料共同给药时,应高度关注ctDNA对酶活性的潜在抑制作用以及前者随后的代谢特性变化。

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