LC-MS-Based Metabolomic Study of Oleanolic Acid-Induced Hepatotoxicity in Mice

被引:18
作者
Feng, Hong [1 ,2 ]
Wu, Ying-Qiu [1 ,2 ]
Xu, Ya-Sha [1 ,2 ]
Wang, Ke-Xin [3 ]
Qin, Xue-Mei [3 ]
Lu, Yuan-Fu [1 ,2 ]
机构
[1] Zunyi Med Univ, Minist Educ, Key Lab Basic Pharmacol, Zunyi, Peoples R China
[2] Zunyi Med Univ, Minist Educ, Joint Int Res Lab Ethnomed, Zunyi, Peoples R China
[3] Shanxi Univ, Modern Res Ctr Tradit Chinese Med, Taiyuan, Peoples R China
关键词
oleanolic acid; metabolomics; hepatotoxicity; bile acid metabolism; LC-MS; CHOLESTATIC LIVER-INJURY; CHROMATOGRAPHY-MASS SPECTROMETRY; BILE-ACIDS; SERUM; PLASMA; TARGET; RATS; FXR;
D O I
10.3389/fphar.2020.00747
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Oleanolic acid (OA), a natural triterpenoid, which has the development prospects in anti-tumor therapy is a widely used hepatoprotective drug in China. It has been reported that OA can cause liver toxicity after higher doses or longer-term use. Therefore, the study aims to explore the possible hepatotoxicity mechanism based on liver metabolic profiles. Liver metabolic profiles were obtained from untargeted ultrahigh performance liquid chromatography (UHPLC)-Q Exactive Orbitrap mass spectrometry (MS) technique. It was found that altered bile acid, amino acid, and energy metabolism might be at least partly responsible for OA-induced hepatotoxicity. Bile acid metabolism, as the most important pathway, was verified by using UHPLC-TSQ-MS, indicating that conjugated bile acids were the main contributors to OA-induced liver toxicity. Our findings confirmed that increased bile acids were the key element of OA hepatotoxicity, which may open new insights for OA hepatotoxicity in-depth investigations, as well as provide a reference basis for more hepatotoxic drug mechanism research.
引用
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页数:12
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