Literature DB >> 22282765

Ingenuity pathways analysis of urine metabolomics phenotypes toxicity of Chuanwu in Wistar rats by UPLC-Q-TOF-HDMS coupled with pattern recognition methods.

Hui Dong1, Aihua Zhang, Hui Sun, Huiyu Wang, Xin Lu, Mo Wang, Bei Ni, Xijun Wang.   

Abstract

Chuanwu (CW), a valuable traditional Chinese medicine (TCM), is the mother root of Aconitum carmichaelii Debx. The cause of CW-induced toxicity is still under ongoing research, although this is limited by the lack of sensitive and reliable biomarkers. Ingenuity pathway analysis (IPA) was performed to analyzing global metabolomics in order to characterize the phenotypically biochemical perturbations and potential mechanisms of the CW-induced toxicity. CW was administered to Wistar rats (0.027 g/200 g and 0.108 g/200 g bw, oral) for 6 months and urine samples were collected. The urinary metabolomics was performed by UPLC-Q-TOF-HDMS, and the mass spectra signals of the detected metabolites were systematically deconvoluted and analyzed by pattern recognition methods (PCA, PLS-DA, and OPLS-DA), revealing a time- and dose-dependency of the biochemical perturbations induced by CW toxicity. As a result, several metabolites responsible for pentose and glucuronate interconversions, alanine, aspartate and glutamate metabolism, starch and sucrose metabolism, amino sugar and nucleotide sugar metabolism, purine metabolism, tryptophan metabolism, taurine and hypotaurine metabolism, fructose and mannose metabolism, fatty acid metabolism were characterized, and it was confirmed that biochemical perturbations can be foreseen from these biomarkers. The urinary metabolomics based IPA with pattern recognition methods also revealed that CW produced serious heart and liver toxicity, consistent with clinical biochemistry and histopathology. Significant changes of 17 metabolites were identified and validated as phenotypic biomarkers of CW toxicity. Overall, our work demonstrated the metabolomics has brought enormous opportunities for improved detection of toxicity and biomarker discovery, highlighting the powerful predictive potential of the IPA to study of drug toxicity.

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Year:  2012        PMID: 22282765     DOI: 10.1039/c1mb05366c

Source DB:  PubMed          Journal:  Mol Biosyst        ISSN: 1742-2051


  20 in total

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Journal:  Pharmacogn Mag       Date:  2014-10       Impact factor: 1.085

7.  A Comparative Metabolomics Approach Reveals Early Biomarkers for Metabolic Response to Acute Myocardial Infarction.

Authors:  Sara E Ali; Mohamed A Farag; Paul Holvoet; Rasha S Hanafi; Mohamed Z Gad
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Authors:  Yi-Fei Li; Jia-Sheng Wu; Yuan-Yuan Li; Yan Dai; Min Zheng; Jia-Kai Zeng; Guo-Feng Wang; Tian-Ming Wang; Wen-Kai Li; Xue-Yan Zhang; Ming Gu; Cheng Huang; Li Yang; Zheng-Tao Wang; Yue-Ming Ma
Journal:  Oncotarget       Date:  2017-09-27

9.  Chemopreventive effects of Ku-jin tea against AOM-induced precancerous colorectal lesions in rats and metabolomic analysis.

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10.  A Metabolomics Profiling Study in Hand-Foot-and-Mouth Disease and Modulated Pathways of Clinical Intervention Using Liquid Chromatography/Quadrupole Time-of-Flight Mass Spectrometry.

Authors:  Cheng Lu; Xinru Liu; Xiaorong Ding; Xiao Chen; Haiwei Fan; Yunqiang Liu; Ning Xie; Yong Tan; Joshua Ko; Weidong Zhang; Aiping Lu
Journal:  Evid Based Complement Alternat Med       Date:  2013-02-19       Impact factor: 2.629

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