Mechanism of Polygonum capitatum in treatment of Helicobacter Pylori associated gastritis by network pharmacology,microarray data analysis and molecular docking北大核心CSCD |
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作者姓名: | 袁艳 杨烨 晏娇艳 何芸 刘敏 莫非 黄健 张姝 |
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作者单位: | 1.贵州医科大学医学检验学院临床检验基础与血液学检验教研室550004;2.贵阳市第一人民医院检验科550002;3.贵州医科大学附属医院临床检验中心550004; |
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基金项目: | 国家自然科学基金资助项目(No 81860723,81960589);中医药、民族医药科学技术基金(No QZYY-2018-019);贵州省科技计划项目[黔科合支撑(2021)一般097]。 |
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摘 要: | Aim To explore the mechanism of Polygonum capitatum(PC)in the treatment of Helicobacter Pylori associated gastritis(HAG). Methods The databases were used to identify the target of PC active compounds and HAG-related genes,and the intersection was taken to obtain the potential targets of PC treatment of HAG. The interaction network diagram of “drug-active compound-target-disease” and the protein-protein interaction(PPI)network of potential target protein interaction in HAG treated by PC were constructed by software Cytoscape 3.6.0. The important nodes in the network were screened by several topological indexes,and the GO and KEGG enrichment were analyzed by STRING database to obtain the potential signaling pathway of PC in the treatment of HAG. The binding ability of PC active components with key target proteins was observed by molecular docking method. On this basis,the related targets of PC in the treatment of HAG were verified in vivo and in vitro experiments. Results The PC active compounds and targets were identified through the database,and the “drug-active compound-target-disease” network diagram and the PPI network of potential target proteins were constructed. Combined with several topological indexes,the PPI network of potential target-protein interaction was analyzed,and 52 hub genes were screened. Further bioinformatics analysis and high-throughput sequencing revealed that PC exerted an effect on HAG through the Akt/NF-κB/NLRP3 pathway. Based on this,it was found that PC could reduce IL-18 and IL-1β in HAG GES-1 cells and HAG SD rats,up-regulate Akt and its phosphorylation level and reduce NF-κB expression,inhibit the activation of NLRP3 inflammatory body,so as to improve HAG inflammatory response. Conclusions PC could exert a therapeutic effect on HAG by activating Akt and its phosphorylation level,and inhibiting the expression of NF-κB and NLRP3 inflammasome related factors. This study provides a theoretical basis for explaining the mechanism of PC in the treatment of HAG. © 2023 Publication Centre of Anhui Medical University. All rights reserved.
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关 键 词: | 头花蓼 幽门螺杆菌相关性胃炎 网络药理学 微阵列数据分析 分子对接 Akt/NF-κB/NLRP3信号通路 |
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