Comprehensive analysis of dihydromyricetin metabolites in rats using ultra-high-performance liquid chromatography coupled with high-resolution mass spectrometry

被引:6
|
作者
Xu Jing [1 ,2 ]
Dong Pingping [2 ]
Cui Yifang [2 ]
Li Huajian [2 ]
Jiang Shan [3 ]
Wang Yong [4 ]
Zhang Jiayu [1 ]
机构
[1] Binzhou Med Univ, Sch Pharm, 346 Guanhai Rd, Yantai 264003, Shandong, Peoples R China
[2] Shandong Univ Tradit Chinese Med, Sch Pharmaceut Sci, 4655 Univ Rd, Jinan 250355, Shandong, Peoples R China
[3] China Acad Chinese Med Sci, Inst Chinese Mat Med, 16 Nanxiao St, Beijing 100700, Peoples R China
[4] Shandong First Med Univ, Shandong Prov Hosp, Dept Tuina, 324 Jingwu Weiqi Rd, Jinan 250098, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
dihydromyricetin; metabolic profile; ultra-high-performance liquid chromatography; Q-Exactive Orbitrap mass spectrometry; AMPELOPSIS-GROSSEDENTATA; IN-VITRO; IDENTIFICATION; APOPTOSIS; MYRICETIN; PROTECTS; PLASMA;
D O I
10.1002/jssc.202200319
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
As the most abundant and bioactive constituent in vine tea (Ampelopsis grossedentata), dihydromyricetin possesses numerous biological activities. A rapid profiling and identification method for dihydromyricetin metabolites in rats after the oral administration has been established using ultra-high-performance liquid chromatography-Q-Exactive Orbitrap mass spectrometry coupled with multiple data-mining methods. Herein, an efficient analytical strategy characterized by a parallel reaction monitoring mode combining diagnostic fragment ions filtering techniques was developed for the comprehensive identification of dihydromyricetin metabolites in rat plasma, urine, and feces. And then, the biotransformation pathways of dihydromyricetin were further revealed. As a result, a total of 49 metabolites were finally identified by comparing diagnostic fragment ions, chromatographic retention times, neutral loss fragment ions, and accurate mass measurement with those of the dihydromyricetin reference standard. These metabolites were presumed to be dominantly generated through hydroxylation, dehydroxylation, methylation, reduction, sulfation, decarbonylation, glucuronidation, glucosylation, and their composite reactions. In a word, our present results not only supplied a solid foundation to better understand the action mechanism of dihydromyricetin, but also provided some models for the metabolism study of the other compounds in traditional Chinese medicines or natural plants.
引用
收藏
页码:3930 / 3941
页数:12
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