UPLC-Q-TOF-MS and network pharmacology to reveal the mechanism of Guizhi Gegen decoction against type 2 diabetes mellitus.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY Naunyn-Schmiedeberg's archives of pharmacology Pub Date : 2025-09-01 Epub Date: 2025-03-17 DOI:10.1007/s00210-025-04011-3
Nini Jia, Jing Li, Mengyao Cui, Yaqing Li, Dayuan Jiang, Xiaoqin Chu
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Abstract

Type 2 diabetes mellitus (T2DM) is a chronic metabolic disease. Clinical studies have shown that the incidence and prevalence of T2DM has been on the rise globally in recent years, and the mortality rate is also increasing. Chinese herbs is multiple target for disease. Guizhi Gegen decoction (GZGGD) is one of the most alternative treatment for T2DM. However, the treatment mechanism is unclear. The composition of the GZGGD was determined by ultra-high-performance liquid chromatography with quadrupole time-of-flight mass spectrometry. The key targets and pathways were predicted by network pharmacology and molecular docking. In vivo experiments were performed to further verify and reveal the potential mechanism of action. We identified 44 active components of GZGGD (genistein, 26-hydroxyporicoic acid DM, puerarin, eugenol, and gentiobiose). Network pharmacology predicted key targets such as TNF, AKT1, TP53, EGFR, and STAT3, and AGE-RAGE, IL-17 signaling pathways were enriched. Molecular docking showed that the active components of GZGGD have good binding activity with the potential targets of T2DM. In vivo animal experiments showed improvement in white blood, fasting blood glucose, and inflammatory factor levels (INS, TC, TNF-α, and IL-6). This study clarifies the potential role of GZGGD in T2DM, which can help in the study of T2DM.

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UPLC-Q-TOF-MS和网络药理学揭示桂枝钩藤煎剂防治2型糖尿病的机制
2型糖尿病(T2DM)是一种慢性代谢疾病。临床研究表明,近年来全球T2DM的发病率和患病率呈上升趋势,死亡率也在不断上升。中药是治疗疾病的多靶点。桂枝葛根汤(GZGGD)是治疗2型糖尿病最具选择性的治疗方法之一。然而,其治疗机制尚不清楚。采用超高效液相色谱-四极杆飞行时间质谱法测定GZGGD的组成。通过网络药理学和分子对接预测了关键靶点和通路。为了进一步验证和揭示其潜在的作用机制,我们进行了体内实验。我们鉴定出了GZGGD的44种有效成分(染料木素、26-羟基茯苓酸DM、葛根素、丁香酚和龙胆糖)。网络药理学预测关键靶点如TNF、AKT1、TP53、EGFR和STAT3, AGE-RAGE、IL-17信号通路丰富。分子对接表明,GZGGD活性成分与T2DM潜在靶点具有良好的结合活性。体内动物实验显示,白细胞、空腹血糖和炎症因子(INS、TC、TNF-α和IL-6)水平均有改善。本研究阐明了GZGGD在T2DM中的潜在作用,有助于T2DM的研究。
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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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