Integration of network pharmacology, bioinformatics and experimental verification strategy to discover the pharmacological mechanisms of mogroside acts against pharyngitis.

IF 4.8 2区 医学 Q1 CHEMISTRY, MEDICINAL
Wu Juanjiang, Huang Huaxue, Chen Guangyu, Mao Jianan, Tian Xing, Zhan Shuang, Peng Zhi, Zhu Yizhun, Wang Wei
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引用次数: 0

Abstract

Ethnopharmacological relevance: Siraitia grosvenorii (Swingle) C. Jeffrey ex Lu & Zhang, a popular herb in traditional Chinese materials, has been broadly employed in food and medicine homology. According to TCM, S. grosvenorii is an essential medicine for clearing the throat and relieving the lungs (Qingyanlifei). However, the bioactive effects of S. grosvenorii on pharyngitis targets remain unclear.

Aim: To determine the active compounds, prospective targets, and the associated molecular mechanisms of S. grosvenorii acts healing pharyngitis. The present study integrated network pharmacology, bioinformatics, molecular docking strategies, and in vitro verification for analysis.

Methods: The active components and potential targets of S. grosvenorii and pharyngitis-related disease targets were sourced from open databases available to the public using network pharmacology approach. The key active components, anti-pharyngitis core targets and pathways were predicted to be obtained by PPI network, GO and KEGG pathway enrichment and bioinformatics analysis. Afterward, molecular docking was executed to estimate the binding interactions of the active constituents with the primary targets. Finally, the key targets predicted via network pharmacology were retrieved from the HPA database, WGCNA, and in vitro trials were performed to further substantiate the outcomes.

Results: A total of 23 bioactive components in S. grosvenorii and 568 herb targets were screened, producing 82 mutual targets in combination with 756 disease targets. GO enrichment analysis incorporated 1708 BP, 49 CC, and 91 MF. KEGG enrichment analysis indicated that the anti-inflammatory effect of mogroside where possessed through a variety of different pathways, including PI3K/AKT and TLR4/NFκB/MyD88 signaling pathway. Probably, the PI3K/AKT signaling pathway has a key impact in S. grosvenorii against pharyngitis. Cell experiments demonstrated that mogroside, the most crucial ingredients on S. grosvenorii, regulated the release of inflammatory cytokines, as well as PI3K/AKT and TLR4/NFκB/MyD88 signaling pathway in LPS-activated RAW264.7 cells, this evidence reinforced the predictions suggested by network pharmacology and molecular docking.

Conclusion: The study extensively identified the biological activities, potential targets and molecular mechanisms of S. grosvenorii in combating pharyngitis through the application of network pharmacology and in vitro assessment. A perspective strategy is provided to offer the scientific foundations and healing mechanism of TCM for pharyngitis treatment.

民族药理学意义:Siraitia grosvenorii (Swingle) C. Jeffrey ex Lu & Zhang 是传统中药中的常用草药,被广泛应用于食物和药物同源中。中医认为,酸枣仁是清肺利咽的要药。目的:确定果味皂苷治疗咽炎的活性化合物、前瞻性靶点及相关分子机制。本研究综合运用网络药理学、生物信息学、分子对接策略和体外验证等方法进行分析:方法:利用网络药理学方法,从公开数据库中获取了咽炎蛇的活性成分和潜在靶点以及咽炎相关疾病的靶点。通过PPI网络、GO和KEGG通路富集和生物信息学分析,预测出关键活性成分、抗咽炎核心靶点和通路。然后进行分子对接,以估计活性成分与主要靶点的结合相互作用。最后,从 HPA 数据库和 WGCNA 中检索了通过网络药理学预测的关键靶点,并进行了体外试验以进一步证实结果:结果:共筛选出 23 种 S. grosvenorii 中的生物活性成分和 568 个草药靶点,结合 756 个疾病靶点得出 82 个共同靶点。GO 富集分析纳入了 1708 个 BP、49 个 CC 和 91 个 MF。KEGG富集分析表明,莫干苷的抗炎作用是通过多种不同途径实现的,包括PI3K/AKT和TLR4/NFκB/MyD88信号通路。PI3K/AKT信号通路可能是葛根皂苷对抗咽炎的关键影响因素。细胞实验表明,蝙蝠蛾皂苷中最关键的成分--蝙蝠蛾皂苷调节了LPS激活的RAW264.7细胞中炎性细胞因子的释放,以及PI3K/AKT和TLR4/NFκB/MyD88信号通路,这一证据加强了网络药理学和分子对接的预测:该研究通过应用网络药理学和体外评估,广泛发现了咽炎蛇的生物活性、潜在靶点和分子机制。为中药治疗咽炎提供了科学依据和治疗机理。
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来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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