Correlative analysis of metabolite profiling of Danggui Buxue Tang in rat biological fluids by rapid resolution LC-TOF/MS

被引:42
作者
Li, Chang-Yin [1 ]
Qi, Lian-Wen [1 ]
Li, Ping [1 ]
机构
[1] China Pharmaceut Univ, Key Lab Modern Chinese Med, Minist Educ, Nanjing 210009, Peoples R China
关键词
Metabolite profiling; Correlative analysis; Rapid resolution LC-TOF/MS; Danggui Buxue Tang; Plasma; Bile; FLIGHT MASS-SPECTROMETRY; BIOACTIVE COMPONENTS; COMBINED PRESCRIPTION; ISOFLAVONE METABOLITES; CELL EXTRACTION; HUMAN URINE; MS ANALYSIS; IN-VITRO; IDENTIFICATION; DECOCTION;
D O I
10.1016/j.jpba.2010.12.034
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
In this work, the metabolite profiles of Danggui Buxue Tang (DBT) in rat bile and plasma were qualitatively described, and the possible metabolic pathways of DBT were subsequently proposed. Emphasis was put on correlative analysis of metabolite profiling in different biological fluids. After oral administration of DBT, bile and plasma samples were collected and pretreated by solid phase extraction. Rapid resolution liquid chromatography coupled to time-of-flight mass spectrometry (RRLC-TOFMS) was used for characterization of DBT-related compounds (parent compounds and metabolites) in biological matrices. A total of 142 metabolites were detected and tentatively identified from the drug-containing bile and plasma samples. Metabolite profiling shows that rat bile contained relatively more glutathione-derived conjugates, more saponins compounds and more diverse forms of metabolites than urine. The metabolite profile in plasma revealed that glucuronide conjugates of isoflavonoids, dimmers, acetylcysteine conjugates and parent form of phthalides, as well as saponin aglycones were the major circulating forms of DBT. Collectively, the metabolite profile analysis of DBT in different biological matrices provided a comprehensive understanding of the in vivo metabolic fates of constituents in DBT. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 160
页数:15
相关论文
共 31 条
[1]
Comparison of genistein metabolism in rats and humans using liver microsomes and hepatocytes [J].
Bursztyka, Julian ;
Perdu, Elisabeth ;
Tulliez, Jacques ;
Debrauwer, Laurent ;
Delous, Georges ;
Canlet, Cecile ;
De Sousa, Georges ;
Rahmani, Roger ;
Benfenati, Emilio ;
Cravedi, Jean-Pierre .
FOOD AND CHEMICAL TOXICOLOGY, 2008, 46 (03) :939-948
[2]
LC-MS-based metabolomics in drug metabolism [J].
Chen, Chi ;
Gonzalez, Frank J. ;
Idle, Jeffrey R. .
DRUG METABOLISM REVIEWS, 2007, 39 (2-3) :581-597
[3]
Measurement of intact sulfate and glucuronide phytoestrogen conjugates in human urine using isotope dilution liquid chromatography-tandem mass spectrometry with [13C3]isoflavone internal standards [J].
Clarke, DB ;
Lloyd, AS ;
Botting, NP ;
Oldfield, MF ;
Needs, PW ;
Wiseman, H .
ANALYTICAL BIOCHEMISTRY, 2002, 309 (01) :158-172
[4]
Identification and Comparison of Metabolites After Oral Administration of Essential Oil of Ligusticum chuanxiong or its Major Constituent Ligustilide in Rats [J].
Ding, Chunguang ;
Sheng, Yuxin ;
Zhang, Yinghao ;
Zhang, Jinlan ;
Du, Guanhua .
PLANTA MEDICA, 2008, 74 (14) :1684-1692
[5]
A chinese herbal decoction prepared from radix astragali and radix angelicae sinensis induces the expression of erythropoietin in cultured Hep3B cells [J].
Gao, Qiu T. ;
Cheung, Jerry K. H. ;
Choi, Roy C. Y. ;
Cheung, Anna W. H. ;
Lv, Jun ;
Jiang, Zhi Y. ;
Duan, Ran ;
Zhao, Kui J. ;
Ding, An W. ;
Dong, Tina T. X. ;
Tsim, Karl W. K. .
PLANTA MEDICA, 2008, 74 (04) :392-395
[6]
Verification of the formulation and efficacy of Danggui Buxue Tang (a decoction of Radix Astragali and Radix Angelicae Sinensis): An exemplifying systematic approach to revealing the complexity of Chinese herbal medicine formulae [J].
Gao Q. ;
Li J. ;
Cheung J.K.H. ;
Duan J. ;
Ding A. ;
Cheung A.W.H. ;
Zhao K. ;
Li W.Z. ;
Dong T.T. ;
Tsim K.W.K. .
Chinese Medicine, 2 (1)
[7]
Identification of isoflavone metabolites dihydrodaidzein, dihydrogenistein, 6′-OH-O-dma, and cis-4-OH-equol in human urine by gas chromatography-mass spectroscopy using authentic reference compounds [J].
Heinonen, S ;
Wähälä, K ;
Adlercreutz, H .
ANALYTICAL BIOCHEMISTRY, 1999, 274 (02) :211-219
[8]
Metabolism of the soy isoflavones daidzein, genistein and glycitein in human subjects.: Identification of new metabolites having an intact isoflavonoid skeleton [J].
Heinonen, SM ;
Hoikkala, A ;
Wähälä, K ;
Adlercreutz, H .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2003, 87 (4-5) :285-299
[9]
Isoflavone metabolites and their in vitro dual functions:: They can act as an estrogenic agonist or antagonist depending on the estrogen concentration [J].
Hwang, Chang Sun ;
Kwak, Ho Seok ;
Lim, Hwa Jae ;
Lee, Su Hee ;
Kang, Young Soon ;
Choe, Tae Boo ;
Hur, Hor Gil ;
Han, Ki Ok .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2006, 101 (4-5) :246-253
[10]
Metabolism of 5-Isopropyl-6-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(2-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine (BMS-645737): Identification of an Unusual N-Acetylglucosamine Conjugate in the Cynomolgus Monkey [J].
Johnson, Benjamin M. ;
Kamath, Amrita V. ;
Leet, John E. ;
Liu, Xiaohong ;
Bhide, Rajeev S. ;
Tejwani, Ravindra W. ;
Zhang, Yueping ;
Qian, Ligang ;
Wei, Donna D. ;
Lombardo, Louis J. ;
Shu, Yue-Zhong .
DRUG METABOLISM AND DISPOSITION, 2008, 36 (12) :2475-2483