Integrating metabolomics and network pharmacology to investigate Da-Chai-Hu Decoction prevents kidney injury in diabetic mice

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL Journal of ethnopharmacology Pub Date : 2025-01-31 Epub Date: 2024-11-27 DOI:10.1016/j.jep.2024.119158
Xue Wang , Zhu-Jun Zhong , Peng-Fei Chen , Chao-Fan Deng , Xiao-Mei Chen , Gui-Zhong Xin , Dan Tang
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Abstract

Ethnopharmacological relevance

The current treatment for diabetic nephropathy (DN) is inadequate, and there is an urgent need for an effective and minimally adverse alternative therapy. Da-Chai-Hu Decoction (DCHD) is a time-honored herbal remedy from Chinese medicine, boasting a legacy spanning more than 1800 years. Clinical observations suggest that it may provide therapeutic benefits for individuals with type 2 diabetes mellitus (T2DM). Nonetheless, the specific advantages of DCHD in relation to DN and the mechanisms through which it operates are still not well understood.

Aim of the study

This research aims to investigate whether DCHD can avert renal damage in mice with T2DM and to elucidate the mechanisms by which DCHD combats DN through the integration of metabolomics and network pharmacology.

Materials and methods

The beneficial effects of DCHD on DN was initially evaluated using a renal injury model in T2DM mice. Subsequently, untargeted metabolomics analysis was utilized to investigate the potential mechanisms of DCHD against DN. Additionally, UPLC-HR MS/MS was employed to identify the chemical components in DCHD and the absorption components in DCHD-treated plasma. Network pharmacology and our newly proposed function-guided and network-based complementary methodology (FNICM) was utilized to predict the potential pathway of DCHD intervention in DN. Finally, the core pathway was validated through Western blotting analysis and ELISA.

Results

A total of 260 chemical components were detected in DCHD, and 41 absorption components were found in DCHD-treated plasma by UPLC-HR MS/MS for the first time. Additionally, In vivo experiments revealed that DCHD exerts the ability to regulate the disorder in glucose/lipid metabolism and improves kidney dysfunction. Furthermore, a comprehensive analysis utilizing non-targeted urine metabolomics and the FNICM method identified a total of 33 differential metabolites, which were categorized as core metabolites. Lastly, combined FNICM, network pharmacology and experimental pharmacology studies suggest that DCHD may regulate the AGEs/RAGE/AKT pathways in combating DN.

Conclusions

The results indicate that DCHD treats DN through the inhibition of the AGEs/RAGE/AKT pathway and by regulating metabolic profiles.

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结合代谢组学和网络药理学研究大柴胡汤对糖尿病小鼠肾损伤的预防作用。
民族药理学相关性:目前对糖尿病肾病(DN)的治疗不足,迫切需要一种有效且不良反应最小的替代疗法。大柴胡汤(DCHD)是一种历史悠久的中草药,拥有1800多年的历史。临床观察表明,它可能为2型糖尿病(T2DM)患者提供治疗益处。尽管如此,DCHD与糖尿病肾病(DN)相关的具体优势及其作用机制仍未得到很好的了解。研究目的:本研究旨在通过代谢组学和网络药理学的结合,探讨DCHD是否可以避免T2DM小鼠的肾脏损害,并阐明DCHD对抗DN的机制。材料与方法:采用T2DM小鼠肾损伤模型,初步评价DCHD对DN的有益作用。随后,利用非靶向代谢组学分析来研究DCHD对抗DN的潜在机制。此外,采用UPLC-MS/MS对DCHD中的化学成分和DCHD处理后血浆中的吸收成分进行鉴定。利用网络药理学和我们新提出的功能引导和基于网络的互补方法学(FNICM)来预测DN中DCHD干预的潜在途径。最后,通过Western blotting分析和ELISA对核心通路进行验证。结果:UPLC-HR MS/MS首次在DCHD处理后的血浆中检出了260种化学成分,41种吸收成分。此外,体内实验表明,DCHD具有调节糖/脂代谢紊乱和改善肾功能的能力。此外,利用非靶向尿液代谢组学和FNICM方法进行综合分析,共鉴定出33种差异代谢物,这些代谢物被归类为核心代谢物。最后,结合FNICM、网络药理学和实验药理学研究表明,DCHD可能调节AGEs/RAGE/AKT通路对抗DN。结论:DCHD通过抑制AGEs/RAGE/AKT通路和调节代谢谱来治疗DN。
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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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