Characterization of oxygenated metabolites of ginsenoside Rg1 in plasma and urine of rat

被引:10
作者
Wang, Jing-Rong [1 ,2 ]
Tong, Tian-Tian [1 ]
Yau, Lee-Fong [1 ]
Chen, Cheng-yu [1 ]
Bai, Li-Ping [1 ,2 ]
Ma, Jing [2 ]
Hu, Ming [3 ]
Liu, Liang [1 ,2 ]
Jiang, Zhi-Hong [1 ,2 ]
机构
[1] Macau Univ Sci & Technol, Macau Inst Appl Res Med & Hlth, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Hongkong Baptist Univ, Sch Chinese Med, Kowloon Tong, Hong Kong, Peoples R China
[3] Univ Houston, Coll Pharm, Dept Pharmacol & Pharmaceut Sci, Houston, TX 77030 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2016年 / 1026卷
基金
美国国家卫生研究院;
关键词
Ginseng; Ginsenoside Rg(1); Oxygenation; Metabolites; PANAX-NOTOGINSENG; GLUCOCORTICOID-RECEPTOR; ALZHEIMERS-DISEASE; MOUSE MODEL; IN-VITRO; RG1; SAPONINS; ABSORPTION; EXCRETION; RB-1;
D O I
10.1016/j.jchromb.2015.12.028
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This study describes the characterization of oxygenated metabolites of ginsenoside Rg(1) in rat urine and plasma. These in vivo metabolites were profiled by using UHPLC-QTOF MS-based method. On the basis of high-resolution MS/MS data, and comparison with chemically synthesized authentic compounds, nine oxygenated metabolites of Rg(1) were characterized as vinaginsenosides 21 and 22 (M1 and M2), vinaginsenoside R15 (M3), 6-O-(beta-D-glucopyranosyl)-20-O-(beta-D-glucopyranosyl) 3 beta, 6 alpha, 12 beta, 20(S)-tetrahydroxy-24-hydroxydammar-25-ene (M4 and M5), floralginsenoside A (M7 and M8), floralginsenoside B (M9) and epoxyginsenoside Rg(1) (M13), respectively. Among these metabolites, M4, M5 and M13 are new ginsenosides and others were detected as in vivo metabolites of Rg(1) for the first time. In addition, a series of oxygenated metabolites of Rh-1 and deglycosylated metabolite of Rg(1), were observed and characterized by comparing with compounds synthesized by us, which revealed an association between C-20 configuration and the extent of oxidation metabolism. Appearance of all these metabolites in blood stream and urine after i.v. dosing and oral administration of Rg(1) was further examined, which clearly showed that mono-oxygenated metabolites of Rg(1) were major circulating metabolites at the early stage after dosing. Characterization of exact chemical structures of these circulating metabolites contribute greatly to our understanding of chemical exposure after consumption of ginseng products, and provide valuable information for explaining multiple bioactivities of ginseng products. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 86
页数:12
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