化学
代谢物
葡萄糖醛酸
生物转化
新陈代谢
色谱法
药代动力学
排泄
代谢途径
毒物动力学
体内
硫酸化
生物化学
药理学
生物
多糖
生物技术
酶
作者
Wenlin Yuan,Zheng-Rui Huang,Sijia Xiao,Ji Ye,Weidong Zhang,Yunheng Shen
出处
期刊:PubMed
日期:2021-12-01
卷期号:46 (23): 6278-6288
被引量:1
标识
DOI:10.19540/j.cnki.cjcmm.20210902.201
摘要
Ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry(UPLC-Q-TOF-MS) was used to investigate the metabolites of maackiain in rats based on the prediction function of UNIFI data processing system and liver microsomal incubation in vitro. Ten metabolites of maackiain after oral absorption were reasonably deduced and characterized. It was found that the biotransformation of maackiain mainly included phase Ⅰ oxidation, dehydrogenation, phase Ⅱ sulfate conjugation, glucosylation conjugation, and glucuronic acid conjugation. Among them, the product of glucosylation conjugation, trifolirhizin, was identified by comparison with the reference for the first time. Liver microsomal incubation in vitro further confirmed the metabolites and metabolic pathways of maackiain in rats. The metabolites in the blood, urine, and feces complemented each other, which revealed the migration, metabolism, and excretion modes of maackiain in rats. This study lays a foundation for the further investigation of the metabolic mechanism of maackiain in vivo and the in-depth research on the mechanism of pharmacodynamics and toxicity.
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