Sun E, Xu Fengjuan, Qian Qian, Cui Li, Tan Xiaobin, Jia Xiaobin
Key Laboratory of New Drug Delivery System of Chinese Materia Medica, Jiangsu Provincial Academy of Chinese Medicine, Nanjing 210028, China.
Key Laboratory of New Drug Delivery System of Chinese Materia Medica, Jiangsu Provincial Academy of Chinese Medicine, Nanjing 210028, China Department of Pharmaceutics, Jiangsu University, Zhenjiang 212013, China.
J Chromatogr Sci. 2016 Feb;54(2):158-64. doi: 10.1093/chromsci/bmv121.
In this work, the metabolite profiles of icariin in rat feces, bile and urine were qualitatively investigated, and the possible metabolic pathways of icariin were subsequently proposed. After oral administration of icariin at a single dose of 100 mg/kg, rat biological samples were collected and pretreated. Then, these pretreated samples were detected by ultraperformance liquid chromatography/quadrupole-time-of-flight mass spectrometry (UPLC-Q-TOF-MS). In all, 17 metabolites were identified in the biosamples. Of these, 5, including F8-F9 (icariside I), D3-D4 (isopentenyl alcohol-icaritin-3-O-rha-7-O-gluA) and N3 (1,3-isoprene icariside II), were to our knowledge reported for the first time. The results indicated that icariin was metabolized via desugarization, dehydrogenation, hydroxylation, demethylation and glucuronidation pathways in vivo. This study revealed the possible metabolite profiles of icariin in rats.
在本研究中,对大鼠粪便、胆汁和尿液中淫羊藿苷的代谢物谱进行了定性研究,并随后提出了淫羊藿苷可能的代谢途径。以100mg/kg的单剂量口服给予淫羊藿苷后,收集大鼠生物样品并进行预处理。然后,通过超高效液相色谱/四极杆-飞行时间质谱(UPLC-Q-TOF-MS)对这些预处理样品进行检测。总共在生物样品中鉴定出17种代谢物。其中,据我们所知,5种代谢物,包括F8-F9(淫羊藿次苷I)、D3-D4(异戊烯醇-淫羊藿苷-3-O-鼠李糖-7-O-葡萄糖醛酸)和N3(1,3-异戊二烯淫羊藿次苷II)是首次报道。结果表明,淫羊藿苷在体内通过去糖基化、脱氢、羟基化、去甲基化和葡萄糖醛酸化途径进行代谢。本研究揭示了大鼠体内淫羊藿苷可能的代谢物谱。