Feng Jixian, Li Yan, Liu Juan, Li Ningli, Sun Bin, Zhao Shizhen, Zhai Yuankun
School of Stomatology, Henan University, Kaifeng, 475000, China.
Kaifeng Key Laboratory of Periodontal Tissue Engineering, Kaifeng, 475000, China.
Heliyon. 2024 Aug 3;10(16):e35744. doi: 10.1016/j.heliyon.2024.e35744. eCollection 2024 Aug 30.
To investigate the material basis, targets and molecular mechanism of against periodontitis to provide theoretical basis for clinical applications.
The active compounds and targets of were obtained from Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) database, and the periodontitis-related targets were collected by integrating Online Mendelian Inheritance in Man (OMIM), Therapeutic Target Database (TTD), Genecards and Gene Expression Omnibus (GEO) database together. The potential targets of against periodontitis were obtained from the intersection of two target sets. Metascape database was used for Gene Ontology (GO) term enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. Discovery Studio software was used for molecular docking between key targets and compounds to evaluate their binding affinity. Western blot was used to check the expression of PTGS2 and MMP9 to verify the regulatory effects of baicalein, the main active compound of , on human periodontal ligament stem cells (hPDLSCs) cultured under inflammatory environment which induced by lipopolysaccharide (LPS).
15 active compounds of and 53 common targets for periodontitis treatment were identified. Among these targets, the 10 core targets were AKT1, IL-6, TNF, VEGFA, TP53, PTGS2, CASP3, JUN, MMP9 and HIF1A. GO and KEGG analysis mainly focused on response to LPS and pathways in cancer. Molecular docking showed that the main active compounds had good binding affinity with key targets. Cell experiments confirmed that baicalein can interfere the expression of pro-inflammatory factors PTGS2 and MMP9 proteins and exert anti-inflammatory effects.
Current study preliminarily analyzed the mechanism of against periodontitis, which provide a new idea for the utilization of and the development of novel medicine for the clinical treatment of periodontitis.
探讨[具体药物名称未给出]治疗牙周炎的物质基础、作用靶点及分子机制,为临床应用提供理论依据。
从中药系统药理学数据库与分析平台(TCMSP)数据库获取[具体药物名称未给出]的活性成分及靶点,并通过整合人类孟德尔遗传在线数据库(OMIM)、治疗靶点数据库(TTD)、基因卡片数据库(Genecards)和基因表达综合数据库(GEO)收集牙周炎相关靶点。从两个靶点集的交集获得[具体药物名称未给出]治疗牙周炎的潜在靶点。利用Metascape数据库进行基因本体(GO)术语富集和京都基因与基因组百科全书(KEGG)通路富集分析。使用Discovery Studio软件进行关键靶点与化合物之间的分子对接,以评估它们的结合亲和力。采用蛋白质免疫印迹法检测环氧化酶-2(PTGS2)和基质金属蛋白酶-9(MMP9)的表达,以验证[具体药物名称未给出]的主要活性成分黄芩苷对脂多糖(LPS)诱导的炎症环境下培养的人牙周膜干细胞(hPDLSCs)的调控作用。
确定了[具体药物名称未给出]的15种活性成分和53个治疗牙周炎的共同靶点。在这些靶点中,10个核心靶点为蛋白激酶B1(AKT1)、白细胞介素-6(IL-6)、肿瘤坏死因子(TNF)、血管内皮生长因子A(VEGFA)、肿瘤蛋白p5(TP53)、环氧化酶-2(PTGS2)、半胱天冬酶-(CASP3)、原癌基因蛋白(JUN)、基质金属蛋白酶-9(MMP9)和缺氧诱导因子-1α(HIF1A)。GO和KEGG分析主要集中在对LPS的反应和癌症相关通路。分子对接表明主要活性成分与关键靶点具有良好的结合亲和力。细胞实验证实黄芩苷可干扰促炎因子PTGS2和MMP9蛋白的表达并发挥抗炎作用。
本研究初步分析了[具体药物名称未给出]治疗牙周炎的机制,为[具体药物名称未给出]的利用及牙周炎临床治疗新药的开发提供了新思路。