Phloretin exhibits potential food-drug interactions by inhibiting human UDP-glucuronosyltransferases in vitro

韧皮部 化学 体外 药理学 药品 生物化学 立体化学 生物
作者
Jinqian Chen,Hao Zhang,Xia Hu,Maowen Xu,Yanjun Su,Chunze Zhang,Yuan Yue,Xiaomin Zhang,Xinyu Wang,Wei Cui,Zhenyu Zhao,Xichuan Li
出处
期刊:Toxicology in Vitro [Elsevier BV]
卷期号:84: 105447-105447 被引量:5
标识
DOI:10.1016/j.tiv.2022.105447
摘要

Phloretin is a well-known apple polyphenol possessing a wide variety of biological effects and has been widely used in many fields. However, it's unclear whether phloretin has an effect on the activity of human UGT enzymes. Our study indicated that phloretin inhibited human UGTs on a broad spectrum. Further kinetic analysis revealed that phloretin inhibited UGT1A1, 1A6, 1A9, 2B7, and 2B15 in a noncompetitive manner, with calculated Ki of 8.34 μM, 16.69 μM, 10.58 μM, 17.74 μM and 2.46μΜ, respectively, whereas phloretin inhibited UGT1A7 in an un-competitive manner, with calculated Ki of 5.70 μM. According to the quantitative risk prediction, co-administration of phloretin with drugs primarily metabolized by UGT1A7 and/or UGT2B15 may result in potential food-drug interactions. To sum up, when phloretin or phloretin-rich food is administered with medications metabolized by UGT1A7 and/or UGT2B15, concern should be exercised.

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