首页|基于HPLC-Q-Exactive Orbitrap-MS和网络药理学探究裸花紫珠颗粒治疗咽炎的作用机制

基于HPLC-Q-Exactive Orbitrap-MS和网络药理学探究裸花紫珠颗粒治疗咽炎的作用机制

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目的 基于高效液相色谱-串联四级杆轨道阱质谱(HPLC-Q-Exactive Orbitrap-MS)方法和网络药理学初步探究裸花紫珠颗粒治疗咽炎的活性成分及潜在作用机制.方法 采用HPLC-Q-Exactive Orbitrap-MS技术分析鉴定裸花紫珠颗粒的主要化学成分,将已定性化合物录入TCMSP、HERB、Swiss Target数据库筛选成分靶点.以"咽炎"为检索词在GeneCards、DisGeNET、Drugbank等数据库中检索疾病相应靶点.裸花紫珠颗粒化学成分对应的靶点与疾病靶点取交集绘制韦恩图,进而运用Cytoscape 3.9.1 软件构建中药-化合物-靶点网络进行可视化,通过Metascape数据库进行GO功能富集分析和KEGG通路富集分析,并绘制气泡图进行可视化.结果 裸花紫珠颗粒共鉴定出 18 种主要化学成分.数据库筛选出 155 个化学成分相应靶点,2319 个咽炎相应靶点,取交集得 76 个相应靶点,根据网络拓扑参数判断关键靶点 38 个.关键靶点涉及丝氨酸/苏氨酸蛋白激酶 1(Akt1)、肿瘤坏死因子(TNF)、肿瘤抑制蛋白P53(TP53)、白细胞介素-6(IL-6)和血管内皮生长因子A(VEGFA)等.GO功能富集分析得到条目 269 个(P<0.01),KEGG通路富集分析筛选得到 116 条信号通路.结论 裸花紫珠颗粒中的化合物能通过多成分、多靶点、多通路防治咽炎,其分子机制与Akt1、TNF、TP53、IL-6 和VEGFA等靶点及芹菜素、木犀草素、咖啡酸等成分相关,涉及TNF通路、白细胞介素-17(IL-17)通路、磷脂酰肌醇激酶(PI3K)-Akt通路、核因子κB(NF-κB)通路、toll样受体通路和丝裂原活化蛋白激酶(MAPK)通路、癌症通路及多糖蛋白和凋亡等信号通路.为后续多靶点药物研发、分子生物学实验及相关临床研究奠定理论基础.
The mechanism of Luohua Zizhu granules in the treatment of pharyngitis based on HPLC-Q-Exactive Orbitrap-MS and network pharmacology
Objective To preliminarily explore the active ingredients and potential mechanism of Luohua Zizhu granules in the treatment of pharyngitis based on high performance liquid chromatography-Q-Exactive Orbitrap-mass spectrometry(HPLC-Q-Exactive Orbitrap-MS)and network pharmacology.Methods HPLC-Q-Exactive Orbitrap-MS was used to analyze and identify the main chemical constituents of Luohua Zizhu granules,and the qualitative compounds were recorded into TCMSP,HERB and Swiss Target databases to screen the component targets.The search term"pharyngitis"was used to search for the corresponding target in GeneCards,DisGeNET,Drugbank and other databases.The intersection of the chemical constituents of Luohua Zizhu granules and the disease targets was plotted as a Wayne diagram,and then the Chinese medicine-compound-target network was constructed and visualized by using Cytoscape 3.9.1 software,and the GO functional enrichment and KEGG pathway enrichment analyses were carried out through the Metascape database and the bubble diagrams were plotted for visualization.Results A total of 18 main chemical components were identified from the granules.The database screened 155 corresponding targets of chemical components,2319 corresponding targets of pharyngitis,and 76 corresponding targets were obtained by taking the intersection,and 38 key targets were judged according to the network topology parameters.The key targets involved serine/threonine protein kinase 1(Akt1),tumor necrosis factor(TNF),tumor suppressor protein P53(TP53),interleukin-6(IL-6)and vascular endothelial growth factor A(VEGFA).GO functional enrichment analysis yielded 269 entries(P<0.01),and KEGG pathway enrichment analysis screened 116 signaling pathways.Conclusion The compounds in Luohua Zizhu granules can prevent and control pharyngitis through multi-components,multi-targets,and multi-pathways,and their molecular mechanisms are related to the targets of Akt1,TNF,TP53,IL-6,and VEGFA,and the components of apigenin,lignocerol,and caffeic acid,which are involved in the TNF pathway,the interleukin-17(IL-17)pathway,the phosphatidylinositol 3-kinase(PI3K)-Akt pathway,the nuclear factor-κB(NF-κB)pathway,the toll-like receptor pathway and the mitogen-activated protein kinase(MAPK)pathway,the cancer pathway and the polysaccharide proteins and apoptosis.It lays a theoretical foundation for subsequent multi-target drug development,molecular biology experiments and related clinical studies.

High performance liquid chromatography-Q-Exactive Orbitrap-mass spectrometryNetwork pharmacologyLuohua Zizhu granulesPharyngitisMechanism

张梅红、周朝忠、晏发、旷春兰、张光磊、王翠、刘厚权、康兴东

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343100 江西普正制药股份有限公司

高效液相色谱-串联四级杆轨道阱质谱 网络药理学 裸花紫珠颗粒 咽炎 作用机制

江西省主要学科学术与技术带头人培养计划领军人才项目

20204BCJ22034

2024

中国实用医药
中国康复医学会

中国实用医药

影响因子:0.797
ISSN:1673-7555
年,卷(期):2024.19(9)
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