Hu Xueyan, Shen Yunbing, Yang Shengnan, Lei Wei, Luo Cheng, Hou Yuanyuan, Bai Gang
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Tianjin Key Laboratory of Molecular Drug Research, Nankai University Tianjin 300350 China
RSC Adv. 2018 Feb 8;8(12):6532-6539. doi: 10.1039/c7ra11856b. eCollection 2018 Feb 6.
Ursolic acid (UA), a pentacyclic terpenoid carboxylic acid widely existing in various medicinal plants, has been reported to have multifarious biological activities such as anti-inflammatory, anticancer and antioxidant activities. In this paper, we analyzed the metabolic profile of UA in mice (including plasma and urine) by using ultra-high performance liquid chromatography (UPLC) coupled with a quadrupole time-of-flight (Q/TOF) method. Principal component analysis (PCA) was applied to differentiate the control and experimental groups. Potential biomarkers were filtered by using loading plots followed by further analysis with UPLC-Q/TOF-MS data. The results showed that 3 metabolites in plasma were identified as markers, one of which was UA and the others were UA epoxides, which belonged to phase I metabolites. Additionally, 5 phase II metabolites were tentatively identified in urine through an accurate mass and characteristic fragment ions. These data suggested that the biotransformation of UA undergoes the major metabolic reactions of the phase I metabolic route of olefin oxidation and phase II metabolic routes of glycine conjugation, glutathione conjugation and glucuronidation. This is the first report of analysis and characterization of the metabolites after the oral administration of UA in mice. The proposed metabolic pathways of UA in mice is also raised for the first time. It might provide further understanding of the potential biological mechanism of UA.
熊果酸(UA)是一种广泛存在于各种药用植物中的五环三萜类羧酸,据报道具有多种生物活性,如抗炎、抗癌和抗氧化活性。在本文中,我们采用超高效液相色谱(UPLC)结合四极杆飞行时间(Q/TOF)方法分析了小鼠体内(包括血浆和尿液)UA的代谢谱。应用主成分分析(PCA)来区分对照组和实验组。通过使用载荷图筛选潜在生物标志物,随后对UPLC-Q/TOF-MS数据进行进一步分析。结果表明,血浆中有3种代谢物被鉴定为标志物,其中一种是UA,其他是UA环氧化物,属于I相代谢物。此外,通过精确质量和特征碎片离子在尿液中初步鉴定出5种II相代谢物。这些数据表明,UA的生物转化经历了烯烃氧化的I相代谢途径的主要代谢反应以及甘氨酸结合、谷胱甘肽结合和葡萄糖醛酸化的II相代谢途径。这是首次报道小鼠口服UA后代谢物的分析和表征。同时也首次提出了UA在小鼠体内的代谢途径。这可能有助于进一步了解UA的潜在生物学机制。