Exploring the bioactive ingredients of three traditional Chinese medicine formulas against age-related hearing loss through network pharmacology and experimental validation.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Wenying Shi, Qi Zhao, Hongwei Gao, Yaxin Yang, Zhiyong Tan, Na Li, Hongjie Wang, Yonghua Ji, You Zhou
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引用次数: 0

Abstract

Traditional Chinese medicine (TCM) formulas, including the Er-Long-Zuo-Ci pill, Tong-Qiao-Er-Long pill, and Er-Long pill, have long been utilized in China for managing age-related hearing loss (ARHL). However, the specific bioactive compounds, pharmacological targets, and underlying mechanisms remain elusive. This study aims to find the shared bioactive ingredients among these three formulas, uncover the molecular pathways they regulate, and identify potential therapeutic targets for ARHL. Furthermore, it seeks to validate the efficacy of these major components through both in vivo and in vitro experiments. Common bioactive ingredients were extracted from the TCMSP database, and their putative target proteins were predicted using the Swiss Target Prediction database. ARHL-related target proteins were collected from GeneCards and OMIM databases. Our approach involved constructing drug-target networks and drug-disease-specific protein-protein interaction networks and conducting clustering, topological property analyses, and functional annotation through GO and KEGG enrichment analysis. Molecular docking analysis was utilized to delineate interaction mechanisms between major bioactive ingredients and key target proteins. Finally, in vivo and in vitro experiments involving ABR recording, immunofluorescent staining, HE staining, and quantitative PCR were conducted to validate the treatment effects of flavonoids on the declining auditory function in DBA/2 J mice. We identified 11 common chemical compounds across the three formulas and their associated 276 putative targets. Additionally, 3350 ARHL-related targets were compiled. As an intersection of the putative targets of the common compounds and ARHL-related proteins, 145 shared targets were determined. Functional enrichment analysis indicated that these compounds may modulate various biological processes, including cell proliferation, apoptosis, inflammatory response, and synaptic connections. Notably, potential targets such as TNFα, MAPK1, SRC, AKT, EGFR, ESR1, and AR were implicated. Flavonoids emerged as major bioactive components against ARHL based on target numbers, with molecular docking demonstrating diverse interaction models between these flavonoids and protein targets. Furthermore, baicalin could mitigate the age-related cochlear damage and hearing loss of DBA/2 J mice through its multi-target and multi-pathway mechanism, involving anti-inflammation, modulation of sex hormone-related pathways, and activation of potassium channels. This study offers an integrated network pharmacology approach, validated by in vivo and in vitro experiments, shedding light on the potential mechanisms, major active components, and therapeutic targets of TCM formulas for treating ARHL.

通过网络药理学和实验验证,探索三种中药配方中抗老年性听力损失的生物活性成分。
在中国,包括二龙左慈丸、通窍二龙丸和二龙丸在内的传统中药配方长期以来一直被用于治疗老年性听力损失(ARHL)。然而,其特定的生物活性化合物、药理靶点和内在机制仍然难以捉摸。本研究旨在找到这三种配方中的共同生物活性成分,揭示其调控的分子通路,并确定治疗 ARHL 的潜在靶点。此外,本研究还试图通过体内和体外实验验证这些主要成分的疗效。研究人员从 TCMSP 数据库中提取了常见的生物活性成分,并使用瑞士靶标预测数据库预测了这些成分的潜在靶标蛋白。与 ARHL 相关的靶蛋白来自 GeneCards 和 OMIM 数据库。我们的方法包括构建药物-靶点网络和药物-疾病特异性蛋白质-蛋白质相互作用网络,并通过GO和KEGG富集分析进行聚类、拓扑特性分析和功能注释。利用分子对接分析来确定主要生物活性成分与关键靶蛋白之间的相互作用机制。最后,我们进行了体内和体外实验,包括 ABR 记录、免疫荧光染色、HE 染色和定量 PCR,以验证黄酮类化合物对 DBA/2 J 小鼠听觉功能下降的治疗效果。我们确定了三种配方中的 11 种常见化合物及其相关的 276 个假定靶点。此外,我们还汇编了 3350 个与 ARHL 相关的靶点。作为常见化合物推测靶点与 ARHL 相关蛋白的交叉点,确定了 145 个共享靶点。功能富集分析表明,这些化合物可能会调节各种生物过程,包括细胞增殖、凋亡、炎症反应和突触连接。值得注意的是,TNFα、MAPK1、SRC、AKT、表皮生长因子受体(EGFR)、ESR1 和 AR 等潜在靶标都与这些化合物有关。根据靶点数量,黄酮类化合物成为抗 ARHL 的主要生物活性成分,分子对接显示这些黄酮类化合物与蛋白质靶点之间存在多种相互作用模型。此外,黄芩苷通过其多靶点、多途径机制,包括抗炎、调节性激素相关途径和激活钾通道,可减轻DBA/2 J小鼠与年龄相关的耳蜗损伤和听力损失。本研究提供了一种综合的网络药理学方法,并通过体内和体外实验进行了验证,揭示了中药配方治疗ARHL的潜在机制、主要活性成分和治疗靶点。
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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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