化学
色谱法
小檗碱
葡萄糖醛酸化
黄连
质谱法
代谢物
硫酸化
羟基化
去甲基化
尿
串联质谱法
高效液相色谱法
代谢途径
代谢组学
新陈代谢
生物化学
微粒体
中医药
医学
基因表达
替代医学
病理
DNA甲基化
基因
酶
作者
Kun Wang,Liwei Chai,Xinchi Feng,Zhongbo Liu,Hongxia Liu,Liqin Ding,Feng Qiu
标识
DOI:10.1016/j.jpba.2017.02.038
摘要
Berberine (BBR), the principle component for many medicinal plants such as Coptis chinensis Franch., Phellodendron chinense Schneid., and Mahonia bealei (Fort.) Carr., possesses diverse pharmacological activities, including anti-bacterial, anti-inflammatory, antitumor, hypolipidemic and antidiabetic activities. In this study, a rapid and reliable method using a five-step strategy based on the ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC/Q-TOF-MS), and metabolynx™ software with mass defect filter (MDF) technique was developed to investigate the metabolism of BBR. Plasma, bile, urine and feces samples were collected from rats after oral administration of BBR with a dose of 100mg/kg/day for three consecutive days and analyzed to characterize the metabolic profile of BBR. By comparing the molecular weights and MS fragmentations of the metabolites with those of the parent drug and reference standards, a total of 97 metabolites were identified, including 68 metabolites in urine, 45 metabolites in plasma, 44 metabolites in bile and 41 metabolites in feces. Demethylation, demethylenation, reduction, hydroxylation, and subsequent glucuronidation, sulfation and methylation were the major metabolic pathways of BBR in vivo.
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