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基于整合药理学的策略探究泻白散治疗小儿肺炎的潜在机制

An Integrated Pharmacology-Based Strategy to Investigate the Potential Mechanism of Xiebai San in Treating Pediatric Pneumonia.

作者信息

Luo Zhuohui, Huang Jiawen, Li Ennian, He Xinqian, Meng Qiqi, Huang Xinan, Shen Xiaoling, Yan Changkai

机构信息

Department of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Beijing, China.

Honz Pharmaceutical Co., Ltd., Haikou, China.

出版信息

Front Pharmacol. 2022 Feb 14;13:784729. doi: 10.3389/fphar.2022.784729. eCollection 2022.

Abstract

Xiebai San (XBS) is a traditional Chinese medicine (TCM) prescription that has been widely used to treat pediatric pneumonia since the Song dynasty. To reveal its underlying working mechanism, a network pharmacology approach was used to predict the active ingredients and potential targets of XBS in treating pediatric pneumonia. As a result, 120 active ingredients of XBS and 128 potential targets were screened out. Among them, quercetin, kaempferol, naringenin, licochalcone A and isorhamnetin showed to be the most potential ingredients, while AKT1, MAPK3, VEGFA, TP53, JUN, PTGS2, CASP3, MAPK8 and NF-κB p65 showed to be the most potential targets. IL-17 signaling pathway, TNF signaling pathway and PI3K-Akt signaling pathway, which are involved in anti-inflammation processes, immune responses and apoptosis, showed to be the most probable pathways regulated by XBS. UPLC-Q/Orbitrap HRMS analysis was then performed to explore the main components of XBS, and liquiritin, quercetin, kaempferol, licochalcone A and glycyrrhetinic acid were identified. Molecular docking analysis of the compounds to inflammation-associated targets revealed good binding abilities of quercetin, kaempferol, licochalcone A and liquiritin to NF-κB p65 and of quercetin and kaempferol to Akt1 or Caspase-3. Moreover, molecular dynamics (MD) simulation for binding of quercetin or kaempferol to NF-κB p65 revealed dynamic properties of high stability, high flexibility and lowbinding free energy. In the experiment with macrophages, XBS markedly suppressed the (Lipopolysaccharides) LPS-induced expression of NF-κB p65 and the production of pro-inflammatory cytokines IL-6 and IL-1β, supporting XBS to achieve an anti-inflammatory effect through regulating NF-κB p65. XBS also down-regulated the expression of p-Akt (Ser473)/Akt, Bax and Caspase-3 and up-regulated the expression of Bcl-2, indicating that regulating Akt1 and Caspase-3 to achieve anti-apoptotic effect is also the mechanism of XBS for treating pediatric pneumonia. Our study helped to reveal the pharmacodynamics material basis as well as the mechanism of XBS in treating pediatric pneumonia.

摘要

泻白散(XBS)是一种中药方剂,自宋代以来就被广泛用于治疗小儿肺炎。为揭示其潜在作用机制,采用网络药理学方法预测泻白散治疗小儿肺炎的活性成分和潜在靶点。结果,筛选出泻白散的120种活性成分和128个潜在靶点。其中,槲皮素、山柰酚、柚皮素、甘草查尔酮A和异鼠李素显示为最具潜力的成分,而AKT1、MAPK3、VEGFA、TP53、JUN、PTGS2、CASP3、MAPK8和NF-κB p65显示为最具潜力的靶点。参与抗炎过程、免疫反应和凋亡的白细胞介素-17信号通路、肿瘤坏死因子信号通路和PI3K-Akt信号通路显示为泻白散最可能调节的通路。随后进行超高效液相色谱-四极杆/轨道阱高分辨质谱(UPLC-Q/Orbitrap HRMS)分析以探究泻白散的主要成分,并鉴定出甘草苷、槲皮素、山柰酚、甘草查尔酮A和甘草次酸。化合物与炎症相关靶点的分子对接分析显示,槲皮素、山柰酚、甘草查尔酮A和甘草苷与NF-κB p65具有良好的结合能力,槲皮素和山柰酚与Akt1或半胱天冬酶-3具有良好的结合能力。此外,槲皮素或山柰酚与NF-κB p65结合的分子动力学(MD)模拟显示出高稳定性、高灵活性和低结合自由能的动力学特性。在巨噬细胞实验中,泻白散显著抑制脂多糖(LPS)诱导的NF-κB p65表达以及促炎细胞因子IL-6和IL-1β的产生,支持泻白散通过调节NF-κB p65发挥抗炎作用。泻白散还下调p-Akt(Ser473)/Akt、Bax和半胱天冬酶-3的表达并上调Bcl-2的表达,表明调节Akt1和半胱天冬酶-3以实现抗凋亡作用也是泻白散治疗小儿肺炎的机制。我们的研究有助于揭示泻白散治疗小儿肺炎的药效物质基础及其作用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1084/8885115/94d2b9080b91/fphar-13-784729-g001.jpg

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