综合肠道微生物组学和超高效液相色谱-质谱代谢组学揭示皮丹江唐颗粒对IGT大鼠的防治机制

IF 6.7 1区 医学 Q1 CHEMISTRY, MEDICINAL Phytomedicine Pub Date : 2024-11-03 DOI:10.1016/j.phymed.2024.156201
Yu Xie, Zirong Li, Yue Fan, Xinyi Liu, Ran Yi, Yaoyao Gan, Zixuan Yang, Shangjian Liu
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引用次数: 0

摘要

简介皮丹降糖汤(PDJT)是根据经典古书《内经》中的 "皮丹 "理论,经验性地用于治疗糖耐量受损(IGT)的传统中药方剂。然而,PDJT干预IGT的机制仍有待研究:本研究旨在通过整合肠道微生物组和 UHPLC-MS 非靶向代谢组学,探讨 PDJT 颗粒干预 IGT 的机制:以6周龄雄性Sprague-Dawley(SD)大鼠为研究对象,采用高脂饮食和注射STZ的方法建立IGT模型。以二甲双胍(Glucophage)为阳性对照药,分别使用低、中、高剂量 PDJT 六周。通过空腹血糖(FBG)、血糖最高值(BGmax)、血脂和炎症因子水平来评估 PDJT 的疗效。最后,通过 16S rDNA 肠道微生物组测序和代谢组学分析,探讨了 PDJT 干预 IGT 的药理机制:结果:PDJT能逆转IGT大鼠的表型,降低血糖水平,改善脂质代谢紊乱,减轻炎症反应。肠道微生物组分析发现,PDJT能改善肠道微生物组的组成和丰度,其中3个门(Firmicutes、Bacteroidota、Desulfobacterota)和4个属(unclassified__f__Lachnospiraceae、Ruminococcus、Allobaculum、Desulfovibrio)在PDJT干预IGT大鼠糖代谢和脂代谢的过程中发挥了重要作用。超高效液相色谱-质谱(UHPLC-MS)非靶向代谢组学研究表明,PDJT可调节脂质代谢通路、炎症反应通路、脂肪和蛋白质消化吸收通路中258种代谢物的水平。这两项全息研究的综合分析表明,通过肠道微生物改善机体代谢可能是 PDJT 治疗 IGT 的可能机制。因此,本研究提供了一种整合肠道微生物组和UHPLC-MS非靶向代谢组学的新方法来评估PDJT干预IGT的药效学和机制,为今后中药治疗IGT的研究提供了宝贵的思路和见解。
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Integrated gut microbiome and UHPLC-MS metabolomics to reveal the prevention mechanism of pidanjiangtang granules on IGT Rats.

Introduction: Pidanjiangtang (PDJT) is a traditional Chinese medicine formula empirically used to treat impaired glucose tolerance (IGT) based on the "Pidan" theory from the classic ancient book Nei Jing. However, the mechanism of PDJT intervention for IGT remains to be studied.

Objective: This study aims to explore the mechanism of PDJT granules intervention in IGT by integrating gut microbiome and UHPLC-MS untargeted metabolomics.

Materials and methods: The IGT model was established in 6-week-old male Sprague-Dawley (SD) rats by feeding them a high-fat diet and using an STZ injection. The low, medium, and high doses of PDJT were used for six weeks. metformin (Glucophage) was used as the positive control drug. The efficacy of PDJT was evaluated using fasting blood glucose (FBG), blood glucose maximum (BGmax), blood lipid, and inflammatory factor levels. Finally, 16S rDNA gut microbiome sequencing with metabolomics analysis was used to explore the pharmacological mechanism of PDJT intervention in IGT.

Results: PDJT could reverse the phenotype of IGT rats, reduce blood glucose levels, improve lipid metabolism disorder, and reduce inflammatory response. Gut microbiome analysis found that PDJT can improve gut microbiota composition and abundance of three phyla (Firmicutes, Bacteroidota, Desulfobacterota) and four genera (unclassified_f__Lachnospiraceae, Ruminococcus, Allobaculum, Desulfovibrio), which play an important role in the process of PDJT intervention on glucose metabolism and lipid metabolism in IGT rats. UHPLC-MS untargeted metabolomics showed that PDJT could regulate the levels of 258 metabolites in lipid metabolism pathways, inflammatory response pathways, fat and protein digestion, and absorption. The combined analysis of the two omics showed that improving the body's metabolism by gut microbes may be the possible mechanism of PDJT in treating IGT. Thus, this study provides a new method to integrate gut microbiome and UHPLC-MS untargeted metabolomics to evaluate the pharmacodynamics and mechanism of PDJT intervention in IGT, providing valuable ideas and insights for future research on the treatment of IGT with traditional Chinese medicine.

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来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
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