黄芪对内毒素诱导的大鼠葡萄膜炎模型影响的网络药理学及实验分析

IF 0.6 4区 医学 Q4 CHEMISTRY, MEDICINAL
Jingmin Lu, Yujie Wu, Yijing Yang, Jing-Wei Zhou, Bo Huang, ChengFeng Xie, Qinghua Peng, Xiaohua Zhang
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引用次数: 0

摘要

目的确定黄芪的关键治疗靶点,探讨黄芪治疗葡萄膜炎的作用机制。从中药系统药理学数据库和分析平台(TCMSP,http://tcmspnw.com)。材料与方法应用Cytoscape软件对葡萄膜炎的疾病靶点进行鉴定。比较了药物靶点和疾病靶点,并将交叉枢纽应用于活性成分靶点网络和蛋白质-蛋白质相互作用(PPI)网络的构建。进行信号通路富集注释,以确定葡萄膜炎治疗中可能涉及的信号传导。建立内毒素诱导的葡萄膜炎(EIU)模型,通过观察眼部症状的改善、组织病理学改变和细胞因子水平,研究黄芪总黄酮(TFA)对葡萄膜炎的治疗作用。结果基于网络药理学分析,HQ可通过NOD样受体(NLR)、细胞凋亡和toll样受体(TLR)信号通路减少细胞因子的产生并调节细胞凋亡,从而调节葡萄膜炎的发生和发展。在动物实验基础上,高剂量TFA可以减少大鼠虹膜充血,减少前房渗出和脓液,恢复瞳孔大小,并减少炎症因子IFN-γ和IL-10的释放。网络药理学和实验分析表明,TFA通过NLR和TLR信号通路调节炎症因子的释放,从而调节EIU大鼠的免疫系统,最终缓解葡萄膜炎大鼠的炎症反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Network Pharmacology and Experimental Analyses on Astragalus membranaceus (Huangqi) Effects on Endotoxin-induced Uveitis Model in Rats
Objectives This study is aimed at identifying critical therapeutic targets of Astragalus membranaceus (Huangqi (HQ)) and investigating the effects and mechanisms of HQ treating uveitis. The potential drug targets of HQ and main active ingredients were obtained from the Traditional Chinese medicine (TCM) systems pharmacology database and analysis platform (TCMSP, http://tcmspnw.com). Materials and Methods Cytoscape software was used to identify the disease targets of uveitis. Drug targets and disease targets were compared, and intersected hubs were applied for the active ingredient-target network and protein-protein-interaction (PPI) network construction. Signaling pathway enrichment annotation was performed to identify possible signaling involved in uveitis treatment. An endotoxin-induced uveitis (EIU) model was established, and the therapeutic effects of total flavonoids of Astragalus (TFA) on uveitis were investigated by examining the improvement of eye symptoms, histopathological alterations, and the levels of cytokines. Results Based on network pharmacological analysis, HQ could modulate the initiation and progression of uveitis by reducing the production of cytokines and regulating cell apoptosis via the NOD-like receptor (NLR), apoptosis, and toll-like receptor (TLR) signaling pathways. Based on animal experiments, high-dose TFA could reduce rat’s iris congestion, reduce anterior chamber exudation and pus, restore pupil size, and decrease the release of inflammatory factors IFN-γ and IL-10. Network pharmacological and experimental analyses revealed that TFA regulates the release of inflammatory factors through the NLR and TLR signaling pathways, thus regulating the immune system of EIU rats and ultimately relieving inflammation responses in uveitis rats.
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来源期刊
Pharmacognosy Magazine
Pharmacognosy Magazine CHEMISTRY, MEDICINAL-
CiteScore
1.87
自引率
0.00%
发文量
37
审稿时长
3 months
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