广东省中药上市后质量与药效再评价工程技术研究中心 / 广东省热带亚热带植物资源重点实验室 / 中山大学生命科学学院,广东 广州 510275
饶鸿宇(1994年生),男;研究方向:中药药理学;E-mail:raohongyu1205@163.com
苏薇薇(1959年生),女;研究方向:创新药物研发、中药上市后质量与药效再评价;E-mail:lsssww@mail.sysu.edu.cn
纸质出版日期:2022-05-25,
网络出版日期:2021-05-20,
收稿日期:2020-07-31,
录用日期:2020-10-14
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饶鸿宇,李沛波,谌攀等.基于网络药理学探讨红核妇洁洗液抗感染的作用机制[J].中山大学学报(自然科学版),2022,61(03):21-27.
RAO Hongyu,LI Peibo,CHEN Pan,et al.Discovery of the active ingredients and the mechanism of action for the effects of Honghe Fujie Lotion on infection based on network pharmacology methods[J].Acta Scientiarum Naturalium Universitatis Sunyatseni,2022,61(03):21-27.
饶鸿宇,李沛波,谌攀等.基于网络药理学探讨红核妇洁洗液抗感染的作用机制[J].中山大学学报(自然科学版),2022,61(03):21-27. DOI: 10.13471/j.cnki.acta.snus.2020E032.
RAO Hongyu,LI Peibo,CHEN Pan,et al.Discovery of the active ingredients and the mechanism of action for the effects of Honghe Fujie Lotion on infection based on network pharmacology methods[J].Acta Scientiarum Naturalium Universitatis Sunyatseni,2022,61(03):21-27. DOI: 10.13471/j.cnki.acta.snus.2020E032.
采用网络药理学方法分析红核妇洁洗液在抗感染过程中发挥功效的潜在靶点和通路,为红核妇洁洗液的机制研究提供参考。首先运用TCMSP、SwissTargetPrediction和CTD数据库检索得到红核洗液中92个化合物的潜在靶标,再检索DisGeNET数据库获得感染性疾病相关靶点,将两者整合去重,得到与抗感染相关的交集靶点合计143个。构建药材-成分-靶点网络后,采用Cytoscape研究该网络的拓扑结构,明确红核妇洁洗液抗感染的关键化合物和潜在作用靶标,主要涉及PARP1、PTGS1、ESR1、IDO1、NOS2、ALOX5、EGFR、PTGS2、HDAC6和JAK1等。将交集靶点导入David数据库进行分析,发现红核洗液主要通过脂多糖介导的通路、TNF 通路、TLR通路和NF-kappa B 通路等发挥抗感染的功效。此外,红核洗液中还能抑制病原菌入侵和繁殖、调节机体免疫应答、减轻炎症反应、缓解机体氧化应激损伤,从而发挥抗感染的作用。
The study aimed to explore the mechanism of anti-infection of Honghe Fujie Lotion (HHFJL) through network pharmacology, and provide a scientific reference for its clinical application. 92 compounds in HHFJL were identified by GC-MS in preliminary studies. The action targets were collected by TCMSP, Toxicogenomics Database (CTD) and SwissTargetPrediction, while the infection related targets were queried through DisGeNET database, and the “compound-disease” intersection targets were obtained using Venn Diagram. The herb- active ingredient- intersection target network was constructed and analysized by Cytoscape. A total of 1 056 targets were collected for HHFJL, and 143 key targets were selected, such as PARP1, PTGS1, ESR1, IDO1, NOS2, ALOX5, EGFR, PTGS2, HDAC6, JAK1, and so on. The results from DAVID indicated that lipopolysaccharide-mediated signaling pathway, NF-kappa B signaling pathway, Toll-like receptor signaling pathway and TNF signaling pathway were the key pathways, which were involved in anti-infective therapies. HHFJL may show therapeutic effects on infection probably through inhibiting pathogenic, regulating immune function, alleviating inflammation and oxidative damage based on multi-target and multi-pathway.
红核妇洁洗液抗感染网络药理学
Honghe Fujie Lotioninfectionnetwork pharmacology
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