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Induction of CYP3As in HepG2 Cells by Several Drugs.-Association between Induction of CYP3A4 and Expression of Glucocorticoid Receptor-

机译:几种药物诱导HepG2细胞中CYP3A的表达-CYP3A4的诱导与糖皮质激素受体表达的相关性

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The cytochrome P-450 3A (CYP3A) enzyme family is responsible for most of the drug metabolism in the human liver. In this study, we demonstrated the inductive effects of phenobarbital, rifampicin, carbamazepine, phenytoin, prednisolone, ciclosporin and clotrimazole on CYP3A4, CYP3A5 and CYP3A7 mRNA expression, and established the relationship between the expression of human glucocorticoid receptor α (hGR) and the induction of CYP3A4 mRNA in cultured HepG2 cells by reverse transcription polymerase chain reaction (RT-PCR). Treatment with prednisolone, rifampicin and carbamazepine rapidly induced the level of CYP3A4 mRNA expression by 3- to 6-fold. The induction of CYP3A4 mRNA expression by clotrimazole and ciclosporin was negligible. Treatment with phenytoin, rifampicin, carbamazepine and ciclosporin induced approximately 2-fold increases in the expression of CYP3A5 mRNA, although prednisolone, phenytoin and clotrimazole had no effect. Treatment with rifampicin, phenytoin, clotrimazole and ciclosporin resulted in approximately a 2-fold induction of the CYP3A7 mRNA level. Treatment with rifampicin and ciclosporin induced the expression of hGRα mRNA significantly in comparison with controls, although the induction of hGRα mRNA following treatment with other drugs was negligible. In cluster analysis, the induced level of CYP3A4, CYP3A5, CYP3A7 and hGRα mRNA by these drugs could be classified into four major clusters. This suggested that each cluster might be associated with different mechanism(s) of induction by these drugs. Further, we studied the associations between the expression of hGRα mRNA and the induced levels of CYP3A4 mRNA by prednisolone and ciclosporin. Treatment with both prednisolone and ciclosporin showed synergistic effects on induction of CYP3A4 mRNA and, following treatment with both drugs, the expression level of CYP3A4 mRNA was 2-fold greater compared with prednisolone alone after then fifth day. Positive correlations were observed between the levels of hGRα mRNA expression and those of CYP3A4 mRNA. This observation shows that the regulation of CYP3A4 gene expression was hGRα-dependent and that ciclosporin may function as a regulator of expression via hGRα.
机译:细胞色素P-450 3A(CYP3A)酶家族负责人类肝脏中的大部分药物代谢。在这项研究中,我们证明了苯巴比妥,利福平,卡马西平,苯妥英钠,泼尼松龙,环孢素和克霉唑对CYP3A4,CYP3A5和CYP3A7 mRNA的诱导作用,并建立了人糖皮质激素受体α(hGR)的表达与诱导的关系。逆转录聚合酶链反应(RT-PCR)检测HepG2细胞中CYP3A4 mRNA的表达。用泼尼松龙,利福平和卡马西平治疗可迅速诱导CYP3A4 mRNA表达水平增加3至6倍。克霉唑和环孢菌素对CYP3A4 mRNA表达的诱导可忽略不计。尽管泼尼松龙,苯妥英钠和克霉唑没有作用,但苯妥英钠,利福平,卡马西平和环孢素的治疗诱导CYP3A5 mRNA表达增加约2倍。用利福平,苯妥英钠,克霉唑和环孢菌素治疗可引起CYP3A7 mRNA水平升高约2倍。与利福平和环孢菌素处理相比,与对照组相比,hGRαmRNA的表达显着提高,尽管用其他药物治疗后hGRαmRNA的诱导可以忽略不计。在聚类分析中,这些药物对CYP3A4,CYP3A5,CYP3A7和hGRαmRNA的诱导水平可分为四大类。这表明每个簇可能与这些药物的诱导机制不同。此外,我们研究了泼尼松龙和环孢素对hGRαmRNA表达与CYP3A4 mRNA诱导水平的关系。泼尼松龙和环孢素的治疗均表现出对CYP3A4 mRNA诱导的协同作用,并且在两种药物治疗后,第五天后CYP3A4 mRNA的表达水平均比单独泼尼松龙高2倍。观察到hGRαmRNA表达水平与CYP3A4 mRNA水平呈正相关。该观察结果表明CYP3A4基因表达的调节是hGRα依赖性的,环孢菌素可能通过hGRα起表达调节剂的作用。

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