Potential molecular mechanisms of Jiedu Tongluo Tiaogan Formula in treating hyperthyroidism based on network pharmacology and in vivo experiments in mice.

IF 2.5 4区 生物学 Q3 CELL BIOLOGY
Physiological genomics Pub Date : 2025-03-01 Epub Date: 2025-01-24 DOI:10.1152/physiolgenomics.00113.2024
Xin Huang, Binqin Chen, Xiaoli Xiao, Chunli Piao
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引用次数: 0

Abstract

"Jiedu Tongluo Tiaoying Formula" (JDTLTYF) is a kind of traditional Chinese medicine (TCM) prescription for treating hyperthyroidism, which can effectively improve the condition of patients. The main active ingredients of JDTLTYF were collected from the traditional Chinese medicine systems pharmacology (TCMSP) database, and the target was predicted. Genes related to hyperthyroidism were identified using DisGeNET, GeneCards, and Online Mendelian Inheritance in Man (OMIM) databases. Protein-protein interaction (PPI) network and interaction network of "formula-herb-active ingredient-target genes" was constructed. Mass spectrometry was used to identify the components. The binding of key components to the target was verified by molecular docking and molecular dynamics (MD) simulations. A hyperthyroidism mouse model was established by using levothyroxine sodium tablets, and the hormone and expression levels of inflammatory factors were examined by ELISA and Western blot. The key genes of JDTLTYF in the treatment of hyperthyroidism were TNF and AKT1. The results of mass spectrometry also showed that quercetin was one of the main components. The results of molecular docking and MD simulation showed that the binding-free energy between AKT1 and quercetin was the lowest, and the binding was stable. In vivo experimental results showed that gastric lavage with JDTLTYF could target AKT1 and TNF-α, effectively alleviate the pathological features of hyperthyroidism in mice, and reduce inflammation response. This study elucidated the key small molecule compounds and their action targets of JDTLTYF in the treatment of hyperthyroidism. It provides a direction for the development of new drugs for clinical hyperthyroidism.NEW & NOTEWORTHY Based on the network pharmacology and molecular dynamics (MD) simulation, this study elucidated the key small molecule compounds and their action targets of JDTLTYF Chinese herbal prescription (debark peony root, common selfheal fruit-spike, figwort root, thunberg fritillary bulb, and oyster shell) in the treatment of hyperthyroidism, preliminarily analyzed its molecular mechanism, and provided a reference direction for subsequent cell experiments.

解毒通络调应方治疗甲亢的潜在分子机制——基于网络药理学和小鼠体内实验。
背景:“解毒通络调应方”(JDTLTYF)中药方剂能有效治疗甲亢,有效改善患者病情。方法:从中药中药药典数据库中提取其主要有效成分,并对其标靶进行预测。使用DisGeNET、GeneCards和OMIM数据库鉴定与甲亢相关的基因。构建了蛋白-蛋白相互作用(PPI)网络和“方剂-中草药-活性成分-靶基因”相互作用网络。采用质谱法对成分进行鉴定。通过分子对接和分子动力学(MD)模拟验证了关键组分与靶标的结合。采用左旋甲状腺素钠片建立甲状腺机能亢进小鼠模型,采用酶联免疫吸附法(ELISA)和免疫印迹法(western blot)检测其激素水平和炎症因子表达水平。结果:JDTLTYF治疗甲亢的关键基因为TNF和AKT1。质谱分析结果也表明槲皮素是其主要成分之一。分子对接和MD模拟结果表明,AKT1与槲皮素的结合自由能最低,结合稳定。体内实验结果显示,用JDTLTYF洗胃可靶向AKT1和TNF-α,有效缓解小鼠甲亢的病理特征,降低炎症反应。结论:本研究阐明了JDTLTYF治疗甲亢的关键小分子化合物及其作用靶点。为临床甲状腺功能亢进新药的开发提供了方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Physiological genomics
Physiological genomics 生物-生理学
CiteScore
6.10
自引率
0.00%
发文量
46
审稿时长
4-8 weeks
期刊介绍: The Physiological Genomics publishes original papers, reviews and rapid reports in a wide area of research focused on uncovering the links between genes and physiology at all levels of biological organization. Articles on topics ranging from single genes to the whole genome and their links to the physiology of humans, any model organism, organ, tissue or cell are welcome. Areas of interest include complex polygenic traits preferably of importance to human health and gene-function relationships of disease processes. Specifically, the Journal has dedicated Sections focused on genome-wide association studies (GWAS) to function, cardiovascular, renal, metabolic and neurological systems, exercise physiology, pharmacogenomics, clinical, translational and genomics for precision medicine, comparative and statistical genomics and databases. For further details on research themes covered within these Sections, please refer to the descriptions given under each Section.
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