In vitro and in silico anti-inflammatory effect of minor constituents from the roots of Polygala arillata Buch.-Ham. ex D. Don.

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED
Bui Thi Thuy Luyen, Tran Anh Quang, Le Xuan Duy, Bui Huu Tai, Nguyen Viet Phong, Do Huu Nghi, Nguyen Minh Khoi, Nguyen Van Chinh, Nguyen Cao Cuong, Trinh Thi Thuy, Tran Thu Huong, Le Ba Vinh, Nguyen Hong Anh, Nguyen Tuan Hiep
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Abstract

Vietnamese traditional medicine has utilised the roots of Polygala arillata Buch.-Ham. ex D. Don to treat acute arthritis, rheumatism, pain, and as a tonic ingredient. In this study, phytochemical analysis of the roots of P. arillata resulted in the isolation of one novel compound, named polygarinolide A (1), along with six known compounds (2-7). High-resolution electrospray ionisation mass spectrometry (HR-ESI-MS) and one- and two-dimensional nuclear magnetic resonance (NMR) spectroscopy were among the spectroscopic techniques used to identify their structures. Additionally, the absolute configuration of compound 1 was determined through ECD calculation. The NO inhibitory activity of purified substances was evaluated. Interestingly, compound 2 exhibited inhibitory activity on NO production in LPS-stimulated RAW264.7 cells (IC50 = 25.37 μM). Moreover, interactions and binding mechanisms of the most active chemical with cyclooxygenase-2 inhibitor (COX-2) and nitric oxide synthase (iNOS) proteins were investigated by molecular docking simulations. Our findings add to our understanding of the secondary metabolites generated by P. arillata and provide a sound scientific basis for future research into the plant's potential anti-inflammatory properties.

远志根部次要成分的体外和体内抗炎作用
越南传统医学利用远志(Polygala arillata Buch.-Ham. ex D. Don)的根来治疗急性关节炎、风湿病和疼痛,并将其作为一种滋补成分。在这项研究中,通过对 arillata 远志的根进行植物化学分析,分离出一种新型化合物,命名为远志内酯 A(1),以及六种已知化合物(2-7)。高分辨率电喷雾离子化质谱(HR-ESI-MS)以及一维和二维核磁共振(NMR)光谱等光谱技术被用来确定它们的结构。此外,还通过 ECD 计算确定了化合物 1 的绝对构型。对纯化物质的 NO 抑制活性进行了评估。有趣的是,化合物 2 在 LPS 刺激的 RAW264.7 细胞中表现出抑制 NO 生成的活性(IC50 = 25.37 μM)。此外,我们还通过分子对接模拟研究了活性最强的化合物与环氧化酶-2 抑制剂(COX-2)和一氧化氮合酶(iNOS)蛋白的相互作用和结合机制。我们的研究结果增加了我们对 arillata P. 产生的次级代谢产物的了解,并为今后研究该植物潜在的抗炎特性提供了可靠的科学依据。
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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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