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Application of metabonomic strategy to discover an unreported active ingredient in LiuWeiDiHuang pills suppressing beta-glucuronidase

机译:代谢组学策略在发现六味地黄丸中抑制β-葡萄糖醛酸苷酶的有效成分中的应用

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Identification of the bioactive ingredient from traditional Chinese medicine (TCM) remains a challenging task by traditional approach that focuses on chemical isolation coupled with biological activity screening. Here, we present a metabonomics-based approach for bioactive ingredient discovery in LiuWeiDiHuang pills (LWPs). First, a non-targeted high-performance liquid chromatography ultraviolet (HPLC-UV) profiling of rat urine was used to discriminate urinary profiling intervened by LWPs. Orthogonal partial least-squares discriminant analysis (OPLS-DA) revealed that eight chromatographic peaks made a significant contribution to the classification of the LWPs group and the control group. Five of these chromatographic peaks were successfully isolated and identified as hippurate, genistein (GT), daidzein (DZ), and glucuronide conjugate of GT and that of DZ by mass spectroscopy (MS). Subsequently, we found that LWPs significantly decreased the activity of intestinal beta-glucuronidase by 18 % and exerted a dose-dependent inhibitory effect on rat liver lysosomal fraction, suggesting that LWPs were a beta-glucuronidase inhibitor. In the end, by inhibiting beta-glucuronidase-guided isolation, d-glucaro-1,4-lactone, a previously unreported ingredient of LWPs, was identified by MS, MS/MS, and nuclear magnetic resonance spectroscopy. Our findings indicated that metabonomics might increase research productivity toward the drug targets and/or bioactive compounds from TCM.
机译:传统方法集中于化学分离和生物活性筛选,从中药(TCM)中鉴定生物活性成分仍然是一项艰巨的任务。在这里,我们提出了一种基于代谢组学的方法来研究六味地黄丸(LWPs)中的生物活性成分。首先,使用大鼠尿液的非靶向高效液相色谱紫外(HPLC-UV)分析来区分LWP介入的尿液分析。正交偏最小二乘判别分析(OPLS-DA)显示,八个色谱峰对LWPs组和对照组的分类做出了重要贡献。已成功分离出其中五个色谱峰,并通过质谱(MS)将其鉴定为马尿酸盐,染料木黄酮(GT),大豆苷元(DZ)和GT和DZ的葡萄糖醛酸苷共轭物。随后,我们发现LWPs显着降低了肠道β-葡萄糖醛酸苷酶的活性18%,并且对大鼠肝溶酶体组分具有剂量依赖性的抑制作用,表明LWPs是β-葡萄糖醛酸苷酶的抑制剂。最后,通过抑制β-葡萄糖醛酸苷酶引导的分离,通过MS,MS / MS和核磁共振波谱鉴定了d-glucaro-1,4-内酯(一种以前未报道的LWPs成分)。我们的发现表明,代谢组学可能会提高针对中药的药物靶标和/或生物活性化合物的研究效率。

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