Anti-hyperuricemic triterpene saponins from the roots of Achyranthes bidentata.

IF 1.6 3区 化学 Q3 CHEMISTRY, APPLIED
Jinqian Yu, Tong Niu, Tao Yue, Xiao Wang, Galabada Arachchige Sirimal Premakumara, Lei Zhao
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Abstract

Three new triterpene saponins (1-3) were obtained from Achyranthes bidentata, which were further assayed for the anti-hyperuricemic activities. Their structures were determined through HRESI-MS, NMR data and chemical method. As for the anti-hyperuricemic evaluation, 1-3 were evaluated against the adenosine/xanthine oxidase induced HK-2 cell model. Compound 1 showed the most effective activity at 50.0 μM, 2 and 3 showed moderate anti-hyperuricemic activities at 50.0 μM and 12.5 μM, respectively, with 1 and 2 concentration-dependent, while 3 on the contrary. Western blot analysis was carried out to investigate the mechanism of 1, demonstrating that 1 reduced uric acid levels partly by regulating the renal urate transporters (OAT1, URAT1 and GLUT9).

牛膝根抗高尿酸三萜皂苷。
从牛膝中分离得到3个新的三萜皂苷(1-3),并对其抗高尿酸血症活性进行了进一步的测定。通过HRESI-MS、NMR数据和化学方法确定了它们的结构。在抗高尿酸血症评价方面,采用腺苷/黄嘌呤氧化酶诱导的HK-2细胞模型评价1-3。化合物1在50.0 μM时表现出最有效的抗高尿酸活性,化合物2和化合物3在50.0 μM和12.5 μM时表现出中等的抗高尿酸活性,化合物1和化合物2具有浓度依赖性,化合物3则相反。Western blot分析1的作用机制,发现1降低尿酸水平部分是通过调节肾尿酸转运蛋白(OAT1、URAT1和GLUT9)。
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来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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