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In vitro evaluation of cytochrome P450 induction and the inhibition potential of mitragynine, a stimulant alkaloid

CYP1A2 CYP3A4型 药理学 生物碱 化学 酶诱导剂 诱导剂 生物信息学 生物化学 细胞色素P450 生物 立体化学 基因
作者
Ee Lin Lim,Tiong Chai Seah,Xue Fen Koe,Habibah A. Wahab,Mohd Ilham Adenan,Mohd Fadzly Amar Jamil,Mohamed Isa Abdul Majid,Mei Lan Tan
出处
期刊:Toxicology in Vitro [Elsevier BV]
卷期号:27 (2): 812-824 被引量:26
标识
DOI:10.1016/j.tiv.2012.12.014
摘要

CYP450 enzymes are key determinants in drug toxicities, reduced pharmacological effect and adverse drug reactions. Mitragynine, an euphoric compound was evaluated for its effects on the expression of mRNAs encoding CYP1A2, CYP2D6 and CYP3A4 and protein expression and resultant enzymatic activity. The mRNA and protein expression of CYP450 isoforms were carried out using an optimized multiplex qRT-PCR assay and Western blot analysis. CYP1A2 and CYP3A4 enzyme activities were evaluated using P450-Glo™ assays. The effects of mitragynine on human CYP3A4 protein expression were determined using an optimized hCYP3A4-HepG2 cell-based assay. An in silico computational method to predict the binding conformation of mitragynine to the active site of the CYP3A4 enzyme was performed and further validated using in vitro CYP3A4 inhibition assays. Mitragynine was found to induce mRNA and protein expression of CYP1A2. For the highest concentration of 25 μM, induction of mRNA was approximately 70% that of the positive control and was consistent with the increased CYP1A2 enzymatic activity. Thus, mitragynine is a significant in vitro CYP1A2 inducer. However, it appeared to be a weak CYP3A4 inducer at the transcriptional level and a weak CYP3A4 enzyme inhibitor. It is therefore, unlikely to have any significant clinical effects on CYP3A4 activity.

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