1H NMR-based metabonomics study of the urinary biochemical changes in Kansui treated rat

被引:49
作者
Tang, Bingwen [2 ]
Ding, Jiajia [2 ]
Wu, Fuhai [3 ]
Chen, Lei [4 ]
Yang, Yongxia [1 ]
Song, Fenyun [2 ]
机构
[1] Guangdong Pharmaceut Univ, Dept Basic Course, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangdong Pharmaceut Univ, Dept Pharm, Guangzhou 510006, Guangdong, Peoples R China
[3] Guangdong Pharmaceut Univ, Sch Publ Hlth, Guangdong Key Lab Mol Epidemiol, Guangzhou 510310, Guangdong, Peoples R China
[4] Chinese Acad Sci, Wuhan Inst Phys & Math, Wuhan Ctr Magnet Resonance, State Key Lab Magnet Resonance & Atom & Mol Phys, Wuhan 430071, Peoples R China
基金
中国国家自然科学基金;
关键词
Kansui; Toxicity; Metabonomics; H-1; NMR; Principal component analysis; MAGNETIC-RESONANCE SPECTROSCOPY; TRADITIONAL CHINESE MEDICINE; AMP-ACTIVATED PROTEIN; EUPHORBIA-KANSUI; H-1-NMR SPECTROSCOPY; CELL-DIVISION; TAURINE; 2-BROMOETHANAMINE; METABOLOMICS; METABOLITES;
D O I
10.1016/j.jep.2012.02.011
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: The dried root of Kansui (Euphorbia kansui L) is a commonly used and effective traditional Chinese medicine (TCM). Aim of the study: We combined the urinary metabolites alteration and traditional assays of Kansui-induced rats to discuss the mechanism of toxicity of Kansui. Materials and methods: The Sprague-Dawley rats were dosed with 7.875 g Kansui/kg weight and 15.75 g Kansui/kg weight. Urine samples were collected at day -1 (before treatment), and days 7, 14 and 21 for NMR analysis. Plasma and liver and kidney tissues were collected at day 14 for biochemical assays and histopathological examination, respectively. Results: The metabonome of rats treated with Kansui differed markedly from that of the controls. This was confirmed by the histopathology of liver and kidney tissue and clinical biochemistry analysis. The toxicity of Kansui accumulated with dosing time, and persisted even when treatment was stopped. The corresponding biochemical pathways alterations included inhibited TCA cycle, increased anaerobic glycolysis, and perturbed amino acids metabolism. Conclusion: The biochemical pathways disorder conjunction with histopathology changes provides new clues to evaluate the toxicity of Kansui from a systematic and holistic view. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:134 / 142
页数:9
相关论文
共 57 条
[1]   1H NMR-based metabonomic analysis of urine from young spontaneously hypertensive rats [J].
Akira, Kazuki ;
Masu, Shigenori ;
Imachi, Misako ;
Mitome, Hidemichi ;
Hashimoto, Miho ;
Hashimoto, Takao .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2008, 46 (03) :550-556
[2]  
[Anonymous], CHINA J MODERN MED
[3]   Metabonomics in Ulcerative Colitis: Diagnostics, Biomarker Identification, And Insight into the Pathophysiology [J].
Bjerrum, Jacob T. ;
Nielsen, Ole H. ;
Hao, Fuhua ;
Tang, Huiru ;
Nicholson, Jeremy K. ;
Wang, Yulan ;
Olsen, Jorgen .
JOURNAL OF PROTEOME RESEARCH, 2010, 9 (02) :954-962
[4]   NMR-Based Metabolic Profiling Identifies Biomarkers of Liver Regeneration Following Partial Hepatectomy in the Rat [J].
Bollard, Mary E. ;
Contel, Nancy R. ;
Ebbels, Timothy M. D. ;
Smith, Leon ;
Beckonert, Olaf ;
Cantor, Glenn H. ;
Lehman-McKeeman, Lois ;
Holmes, Elaine C. ;
Lindon, John C. ;
Nicholson, Jeremy K. ;
Keun, Hector C. .
JOURNAL OF PROTEOME RESEARCH, 2010, 9 (01) :59-69
[5]   Metabolic Signatures of Lung Cancer in Biofluids: NMR-Based Metabonomics of Urine [J].
Carrola, Joana ;
Rocha, Claudia M. ;
Barros, Antonio S. ;
Gil, Ana M. ;
Goodfellow, Brian J. ;
Carreira, Isabel M. ;
Bernardo, Joao ;
Gomes, Ana ;
Sousa, Vitor ;
Carvalho, Lina ;
Duarte, Iola F. .
JOURNAL OF PROTEOME RESEARCH, 2011, 10 (01) :221-230
[6]  
Chinese Pharmacopoeia Committee, 2010, PHARM CHIN
[7]   An hypothesis for a mechanism underlying hepatotoxin-induced hypercreatinuria [J].
Clayton, TA ;
Lindon, JC ;
Everett, JR ;
Charuel, C ;
Hanton, G ;
Le Net, JL ;
Provost, JP ;
Nicholson, JK .
ARCHIVES OF TOXICOLOGY, 2003, 77 (04) :208-217
[8]   Taurine attenuates calcium-dependent, Fas-mediated neutrophil apoptosis [J].
Condron, C ;
Neary, P ;
Toomey, D ;
Redmond, HP ;
Bouchier-Hayes, D .
SHOCK, 2003, 19 (06) :564-569
[9]  
Deng Y., 2008, TRAD CHIN MED P
[10]  
Diao Y. P., 2007, ADVERSE DRUG REACT J, V9, P243