Feng Hong, Wu Ying-Qiu, Xu Ya-Sha, Wang Ke-Xin, Qin Xue-Mei, Lu Yuan-Fu
Key Laboratory of Basic Pharmacology of the Ministry of Education and Joint International Research Laboratory of Ethnomedicine of the Ministry of Education, Zunyi Medical University, Zunyi, China.
Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan, China.
Front Pharmacol. 2020 May 26;11:747. doi: 10.3389/fphar.2020.00747. eCollection 2020.
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.
齐墩果酸(OA)是一种天然三萜类化合物,在中国是一种广泛使用的保肝药物,在抗肿瘤治疗方面具有发展前景。据报道,高剂量或长期使用OA会导致肝脏毒性。因此,本研究旨在基于肝脏代谢谱探索可能的肝毒性机制。肝脏代谢谱通过非靶向超高效液相色谱(UHPLC)-Q Exactive Orbitrap质谱(MS)技术获得。研究发现,胆汁酸、氨基酸和能量代谢的改变可能至少部分导致了OA诱导的肝毒性。作为最重要的途径,胆汁酸代谢通过UHPLC-TSQ-MS得到验证,表明结合型胆汁酸是OA诱导肝脏毒性的主要因素。我们的研究结果证实,胆汁酸增加是OA肝毒性的关键因素,这可能为深入研究OA肝毒性开辟新的思路,并为更多肝毒性药物机制研究提供参考依据。