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The Study on Biotransformation of Paeonol and Interrelation with Cytochrome P450 Enzymes

机译:丹皮酚的生物转化及其与细胞色素P450酶的相互关系的研究

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Objective: Metabolic enzymes and biotransformation of paeonol were studied by extraorgan incubation method in homogenized liver, and rational clinical administration method of paeonol was provided with scientific evidences. Methods: The content of surplus paeonol in the homogenized liver incubation solution was detected by HPLC, and the effects of inductors and inhibitors in metabolism of paeonol were analyzed, besides metabolites and metabolic pathways of paeonol were investigated by HPLC/MS/MS. Results: The metabolic rate of paeonol in Dexamethasone (DEX) group which is the main CYP3A inductor, was significantly higher than it of the control group, however, the Phenobarbital (PB) group which is the main CYP2B inductor, had no significant difference in the metabolic rate of paeonol with control group,moreover, Meletin, the specific CYP3A inhibitor, could significantly inhibit the metabolism of paeonol; the metabolites of paeonol in rat homogenized liver were 4-methoxyacetophenone-2-O-glucuronide and 2,4-dihydroxyacetophenone-5-O-sulphate. Conclusion: CYP3A is the main enzyme taking part in the biotransformation of paeonol in rats, and the paenol administrating simultaneously with the medicines, which have inducing and inhibiting effects on CYP3A, may probably have interactions.
机译:目的:通过器官外匀培养法研究pa药的代谢酶和Meta药的生物转化,为合理的eon药临床给药方法提供科学依据。方法:采用高效液相色谱法测定均质肝培养液中多余的丹皮酚含量,分析诱导剂和抑制剂对丹皮酚代谢的影响,并通过HPLC / MS / MS研究丹皮酚的代谢产物和代谢途径。结果:地塞米松(DEX)组是主要的CYP3A诱导剂,其丹皮酚的代谢速率显着高于对照组,而苯巴比妥(PB)组是主要的CYP2B诱导剂,在代谢组中无显着差异。 pa药的代谢率与对照组相比,CYP3A特异抑制剂Meletin能显着抑制pa药的代谢。大鼠均质肝中丹皮酚的代谢产物为4-甲氧基苯乙酮-2-O-葡糖醛酸和2,4-二羟基苯乙酮-5-O-硫酸盐。结论:CYP3A是参与大鼠丹皮酚生物转化的主要酶,与该药同时使用对大鼠CYP3A有诱导和抑制作用,可能具有相互作用。

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