期刊文献+

基于网络药理学和蛋白模块探讨培土清心颗粒治疗特应性皮炎的作用机制 被引量:9

Study on the Mechanism of Peitu Qingxin Granules in the Treatment of Atopic Dermatitis Based on Network Pharmacology and Protein Module
原文传递
导出
摘要 目的运用网络药理学和蛋白模块方法探讨培土清心颗粒治疗特应性皮炎(atopic dermatitis,AD)的作用机制。方法基于中药系统药理学数据库及分析平台(TCMSP)和BATMAN-TCM数据库获取培土清心颗粒化学成分及其对应靶点,通过GeneCards、OMIM、DisGeNET数据库筛选特应性皮炎疾病靶点。使用String数据库构建蛋白相互作用(PPI)网络;使用Cytoscape软件绘制培土清心颗粒潜在活性成分-靶点-疾病网络图,使用Network Analyzer工具对网络进行拓扑属性分析;以插件ClusterMaker对靶点进行模块化分解,并使用DAVID数据库进行基因百科全书(KEGG)通路富集分析。结果得到培土清心颗粒治疗特应性皮炎活性成分185个,靶点125个,重要活性成分包括檞皮素、木犀草素、山奈酚、汉黄芩素等;重要靶点包括PTGS2、CXCL8、IL-10、CCL2等;PPI网络模块化分析结果显示,125个靶点主要分为3个模块,KEGG通路富集方面,模块一内靶点KEGG通路主要与特应性皮炎免疫系统、炎症反应相关;模块二内靶点KEGG通路主要与细胞增殖、分化、凋亡相关;模块三内靶点KEGG通路与代谢密切相关。结论培土清心颗粒可能通过抗炎、调节免疫、调控细胞凋亡以及调节氨基酸代谢以达到治疗特应性皮炎的目的。 Objective To explore the mechanism of Peitu Qingxin granules in the treatment of atopic dermatitis(atopic dermatitis,AD)by means of network pharmacology and protein module.Methods The chemical constituents and corresponding targets of Peitu Qingxin granules were obtained based on the traditional Chinese medicine system pharmacology database and analysis platform(TCMSP)and BATMAN-TCM database,and the disease targets of AD were screened by Gene Cards,OMIM and DisGeNET databases.String database was used to construct protein interaction(PPI)network.Cytoscape software was used to draw the potential active component-target-disease network map of Peitu Qingxin granules.We analyzed the topological properties of the network by Network Analyzer tool.Then,plug-in ClusterMaker was used to modularize the targets,and DAVID database was used for Kyoto Encyclopedia of Gene and Genomes(KEGG)pathway enrichment analysis.Results 185 active components and 125 targets of Peitu Qingxin granules were obtained.Quercetin,luteolin,kaempferol and wogonin were the main ingredients in Peitu Qingxin granules.And the key targets were PTGS2,CXCL8,IL-10 and CCL2.The results of PPI network modularization analysis showed that the 125 targets were mainly divided into three modules.In the aspect of KEGG pathway enrichment,targets are mainly related to AD immune system and inflammation in module one,the pathways of module two targets are mainly related to cell proliferation,differentiation and apoptosis,and targets are closely related to metabolism in module three.Conclusion Peitu Qingxin granules may treat AD by antiinflammation,regulating immunity,regulating apoptosis and regulating amino acid metabolism.
作者 秦爽 莫秀梅 陈达灿 QIN Shuang;MO Xiumei;CHEN Dacan(Second School of Clinical Medicine,Guangzhou University of Chinese Medicine,Guangzhou 510405 Guangdong,China;Guangdong Provincial Hospital of Chinese Medicine,Guangzhou 510120 Guangdong,China)
出处 《中药新药与临床药理》 CAS CSCD 北大核心 2021年第2期191-199,共9页 Traditional Chinese Drug Research and Clinical Pharmacology
基金 国家自然科学基金项目(81774307) 广东省中医药防治难治性慢病重点实验室(中医二院[2019]78号,2018B030322012)。
关键词 培土清心颗粒 特应性皮炎 网络药理学 蛋白模块 信号通路 抗炎 免疫调节 细胞 凋亡 氨基酸代谢 Peitu Qingxingranules atopic dermatitis network pharmacology protein module signal pathway anti-inflammatory immunomodulatory cells apoptosis amino acid metabolism
  • 相关文献

参考文献7

二级参考文献69

  • 1黄继汉,黄晓晖,陈志扬,郑青山,孙瑞元.药理试验中动物间和动物与人体间的等效剂量换算[J].中国临床药理学与治疗学,2004,9(9):1069-1072. 被引量:1369
  • 2王明雷,王素贤,孙启时.白茅根化学及药理研究进展[J].沈阳药科大学学报,1997,14(1):67-69. 被引量:28
  • 3胡竟一,雷玲,余悦,邓文龙.连翘的抗炎解热作用研究[J].中药药理与临床,2007,23(3):51-52. 被引量:94
  • 4赵辩.中国临床皮肤病学[M].南京:江苏科学技术出版社,2009:573-577.
  • 5陈达灿,范瑞强.皮肤性病专病中医临床诊治[M].3版.北京:人民卫生出版社,2013:67-98.
  • 6Lee J, Bielory L. Complementary and alternative interventions in atopie dermatitis [ J ]. Immunol Allergy Clin North Am, 2010,30 (3) :411-424.
  • 7张海玉,李常胜,塔娜.蒙药雄银散抗炎作用的初步研究[J].实用临床医药,2013,32(3):9-10.
  • 8Nitin GargJonathan I.Silverberg.Epidemiology of c+ldhood atopic dermatitis.Clinics in Dermatology,2015,33(3):281-288.
  • 9Matsushita T,Tedder T F.Identifying regulatory B cells(B10 cells) that produce IL-10 in mice.Methods Mol Biol,2011,677:99-111.
  • 10Liu J,Mo X,Wu D,et al.Efficacy of a Chinese herbal medicine for the treatment of atopic dermatitis:A randomised controlled study. Complement Ther Med,2015,23(5):644-651.

共引文献61

同被引文献112

引证文献9

二级引证文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部