Integrating 16S rDNA sequencing analysis and targeted metabolomics to explore the mechanism of Xiexin Tang in treating atherosclerosis mice induced by high-fat diet

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL Journal of pharmaceutical and biomedical analysis Pub Date : 2025-07-15 Epub Date: 2025-02-25 DOI:10.1016/j.jpba.2025.116760
Junling Li , Qianru Gao , Hongtao Liu , Songlin Liu , Yanchun Wang , Xiongjie Sun , Junping Zheng , Huabing Yang , Baifei Hu
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Abstract

Xiexin Tang (XXT) is a classic Chinese medicine formula that can be used to treat Atherosclerosis (AS). This study aimed to investigate the mechanism by which XXT regulated AS lipid levels. Firstly, the mixture components of XXT were analyzed by High-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Then, the AS model based on Apolipoprotein E knockout (ApoE-/-) mice was established. Cytokines related to lipid metabolism and bile acid metabolism were detected by Quantitative Real-time PCR (qRT-PCR). 16S rDNA gene sequencing was performed to analyze differential bacterial populations, and the mechanism of XXT regulation of bile acids affecting lipid metabolism was further explored by targeted metabolomics. Further, antibiotic-treated mice were used to investigate the role of gut microbiota in the anti-AS effect of XXT. The results showed that XXT attenuated the lipid levels and reversed the abnormal elevation of cytokines, such as hepatic lipid metabolism and inflammatory reaction in AS mice. XXT also repaired the gut barrier damage and reversed gut microbiota disorders in AS mice. Furthermore, the metabolic levels of bile acids were reshaped by XXT. Whereas, in the absence of gut microbiota, XXT failed to attenuate lipid levels and inhibit the expression of cytokines related to inflammation and bile acid metabolism in AS mice and failed to play a role in ultimately treating AS. In conclusion, XXT could effectively inhibit the inflammatory reaction and lipid accumulation in AS mice, and this effect was closely related to its remodeling of gut microbiota to regulate bile acid metabolism.
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结合16S rDNA测序分析和靶向代谢组学,探讨泻心汤治疗高脂饮食致动脉粥样硬化小鼠的作用机制
泻心汤是治疗动脉粥样硬化(AS)的经典中药方剂。本研究旨在探讨XXT调节AS脂质水平的机制。首先,采用高效液相色谱-串联质谱(HPLC-MS/MS)对XXT的混合组分进行分析。然后建立载脂蛋白E敲除(ApoE-/-)小鼠AS模型。采用实时荧光定量PCR (qRT-PCR)检测与脂质代谢和胆汁酸代谢相关的细胞因子。通过16S rDNA基因测序分析差异菌群,通过靶向代谢组学进一步探索XXT调控胆汁酸影响脂质代谢的机制。此外,使用抗生素治疗的小鼠来研究肠道微生物群在XXT抗as作用中的作用。结果表明,XXT能降低as小鼠的脂质水平,逆转肝脏脂质代谢和炎症反应等细胞因子的异常升高。XXT还能修复AS小鼠的肠道屏障损伤和逆转肠道微生物群紊乱。此外,胆汁酸的代谢水平被XXT重塑。然而,在缺乏肠道微生物群的情况下,XXT不能降低AS小鼠的脂质水平,也不能抑制与炎症和胆汁酸代谢相关的细胞因子的表达,也不能在最终治疗AS中发挥作用。综上所述,XXT能有效抑制AS小鼠的炎症反应和脂质积累,其作用与其重塑肠道菌群调节胆汁酸代谢密切相关。
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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