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连花清瘟治疗新型冠状病毒肺炎及面神经炎的药理作用机制

Pharmacological mechanism of action of Lianhua Qingwen in the treatment of COVID-19 and facial neuritis.

作者信息

Li Guang-Jin, Hao Zhi-Hong, Wang Han-Jing, Wang Chen, Liu Da-Wei, Chen Liang, Sun Yan

机构信息

Department of Otorhinolaryngology The Second Affiliated Hospital of Guilin Medical University Guilin Guangxi China.

Department of Otorhinolaryngology Head and Neck Surgery The Affiliated Yantai Yuhuangding Hospital of Qingdao University Yantai Shandong China.

出版信息

World J Otorhinolaryngol Head Neck Surg. 2024 May 30;11(1):102-115. doi: 10.1002/wjo2.185. eCollection 2025 Mar.

Abstract

OBJECTIVE

Coronavirus disease-2019 (COVID-19) can cause not only respiratory symptoms but also facial paralysis. Lianhua Qingwen (LHQW) has been reported to have therapeutic effects on COVID-19 and facial neuritis (FN). We explored the potential mechanism of LHQW in the treatment of COVID-19 and FN through a network-pharmacology approach.

METHODS

Active compounds and relevant targets of LHQW were obtained from the databases of Traditional Chinese Medicine Systems Pharmacology Database, HERB, UniProt Knowledge Base, SwissADME, and Swiss Target Prediction. Disease targets of COVID-19 and FN were acquired from Gene Cards. Database For Annotation, Visualization And Integrated Discovery and Metascape were used to search the biological functions of intersecting targets. After identifying the core targets and their corresponding ingredients, KEGG Mapper analyzes the localization of core targets in key pathways. AutoDock were employed to conduct molecular docking of the core targets and their corresponding ingredients.

RESULTS

We obtained four core genes: interleukin (IL)-8, IL-1B, IL-6, and tumor necrosis factor (TNF)-α. Database searching revealed the anti-inflammatory and antiviral effects of LHQW may be related to the action of aleo-emodin, hyperforin, kaempferol, luteolin, and quercetin on these four genes by regulating the pathways of IL-17 and NOD-like receptor. The molecular-docking results of the four core targets and their corresponding active ingredients showed good binding activity between receptors and ligands.

CONCLUSIONS

We uncovered the active ingredients, potential targets, and biological pathways of LHQW for COVID-19 and FN coinfection. Our data provide a theoretical basis for further exploration of the mechanism of action of LHQW in treatment of COVID-19 and FN.

摘要

目的

2019冠状病毒病(COVID-19)不仅可引起呼吸道症状,还可导致面瘫。据报道,连花清瘟(LHQW)对COVID-19和面部神经炎(FN)具有治疗作用。我们通过网络药理学方法探讨了连花清瘟治疗COVID-19和FN的潜在机制。

方法

从中药系统药理学数据库、HERB、UniProt知识库、SwissADME和Swiss Target Prediction数据库中获取连花清瘟的活性成分和相关靶点。从基因卡片中获取COVID-19和FN的疾病靶点。使用注释、可视化和综合发现数据库以及Metascape搜索交叉靶点的生物学功能。在确定核心靶点及其相应成分后,KEGG Mapper分析核心靶点在关键途径中的定位。采用AutoDock对核心靶点及其相应成分进行分子对接。

结果

我们获得了四个核心基因:白细胞介素(IL)-8、IL-1B、IL-6和肿瘤坏死因子(TNF)-α。数据库检索显示,连花清瘟的抗炎和抗病毒作用可能与芦荟大黄素、金丝桃素、山奈酚、木犀草素和槲皮素通过调节IL-17和NOD样受体途径对这四个基因的作用有关。四个核心靶点及其相应活性成分的分子对接结果显示受体与配体之间具有良好的结合活性。

结论

我们揭示了连花清瘟治疗COVID-19和FN合并感染的活性成分、潜在靶点和生物学途径。我们的数据为进一步探索连花清瘟治疗COVID-19和FN的作用机制提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/760d/11891286/04495f138f34/WJO2-11-102-g010.jpg

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