姜黄素
CYP3A型
药理学
槲皮素
华法林
CYP1A2
CYP2C9
微粒体
化学
药物相互作用
药物代谢
CYP3A4型
细胞色素P450
药品
体外
生物化学
生物
新陈代谢
医学
抗氧化剂
心房颤动
内科学
作者
Viktoriia Burkina,Galia Zamaratskaia,Martin Krøyer Rasmussen
出处
期刊:Xenobiotica
[Taylor & Francis]
日期:2022-05-04
卷期号:52 (5): 435-441
被引量:4
标识
DOI:10.1080/00498254.2022.2089932
摘要
The anticoagulant drug warfarin is used treat atrial fibrillation. Several cases of drug-drug and drug-food interactions have been reported for warfarin.The aim of this study was to investigate the interaction between simultaneous administration of warfarin with the two ubiquitous flavonoids quercetin and curcumin.Using porcine primary hepatocytes we demonstrated that warfarin treatment increased the mRNA and protein expression of CYP3A(29), while no changes in CYP1A2 were observed. Co-treatment with quercetin and/or curcumin decreased the warfarin-induced CYP3A protein expression. Moreover, when quercetin and curcumin were co-administrated to warfarin-exposed hepatocytes the protein expression of CYP1A2 was decreased. In hepatic microsomes, curcumin inhibited the activity of both CYP1A2 and CYP3A, while warfarin had no effect. Both quercetin and curcumin decreased the CYP1A2 and CYP3A activity when co-administrated with warfarin.The results clearly demonstrated that quercetin and curcumin can cause food-drug interactions with warfarin, and that the cocktail effect of exposure to more compounds than one can further enhance these interactions.
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