[Blood glucose-lowering mechanism of Poria aqueous extract by UPLC-Q-TOF-MS/MS combined with network pharmacology and experimental verification].

Q3 Pharmacology, Toxicology and Pharmaceutics
Dan-Dan Zhang, Wen-Biao Wan, Qing Yao, Fang Li, Zi-Yin Yao, Xiao-Chuan Ye
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引用次数: 0

Abstract

Ultra performance liquid chromatography-quadrupole-time-of-flight-mass spectrometry/mass spectrometry(UPLC-Q-TOF-MS/MS), network pharmacology, and animal experiments were integrated o explore the blood glucose-lowering effects and mechanisms of Poria aqueous extract. Firstly, the active components of Poria aqueous extract were identified by UPLC-Q-TOF-MS/MS. Subsequently, network pharmacology was employed to predict the blood glucose-lowering components and mechanisms of Poria aqueous extract. Finally, a rat model of diabetes mellitus, 16S rDNA sequencing, and Western blot were employed to investigate the blood glucose-lowering effect and mechanism of Poria aqueous extract. A total of 39 triterpenoids were identified in the Poria aqueous extract, among them, 25-hydroxypachymic acid, 25α-hydroxytumulosic acid, 16α-hydroxytrametenolic acid, polyporenic acid C, and tumulosic acid may be the main active ingredients for treating diabetes. The Kyoto Encyclopedia of Genes and Genomes(KEGG) pathway enrichment analysis revealed that Poria might exert its therapeutic effects through multiple pathways such as NOD-like receptor signaling pathway, nuclear factor-kappa B(NF-κB) signaling pathway, and tumor necrosis factor(TNF) signaling pathway. The results of animal experiments demonstrated that Poria aqueous extract significantly reduced the levels of blood glucose and lipids and regulated the intestinal flora in diabetic rats. The main affected taxa included g_Escherichia-Shigella, g_Corynebacterium, g_Prevotella_9, g_Prevotellaceae_UCG-001, and g_Bacteroidota_unclassified. In addition, Poria aqueous extract lowered the levels of D-lactic acid and lipopolysaccharide, alleviated colonic mucosal damage, significantly down-regulated the protein levels of NOD-like receptor pyrin domain-containing protein 3(NLRP3), NF-κB, and TNF-α, and significantly up-regulated the protein levels of zonula occludens 1 and occludin in diabetic rates. Poria aqueous extract may play a role in treating diabetes mellitus by repairing the intestinal flora disturbance, protecting the intestinal barrier function, and inhibiting the NF-κB/NLRP3 signaling pathway. The results provide a scientific basis for clinical application and expansion of indications of Poria.

[UPLC-Q-TOF-MS/MS结合网络药理学及实验验证茯苓水提物的降血糖机制]。
采用超高效液相色谱-四极杆飞行时间质谱/质谱(UPLC-Q-TOF-MS/MS)、网络药理学和动物实验相结合的方法,探讨茯苓水提物的降血糖作用及其机制。首先,采用UPLC-Q-TOF-MS/MS对茯苓水提物的有效成分进行鉴定。随后,采用网络药理学方法对茯苓水提物的降血糖成分及作用机制进行了预测。最后,采用糖尿病大鼠模型、16S rDNA测序、Western blot等方法研究茯苓水提物的降血糖作用及其机制。茯苓水提物中共鉴定出39种三萜类化合物,其中25-羟基草酸、25α-羟基瘤酸、16α-羟基曲烯酸、聚聚二烯酸C和瘤酸可能是茯苓水提物治疗糖尿病的主要有效成分。京都基因基因组百科(KEGG)通路富集分析显示,茯苓可能通过nod样受体信号通路、核因子κB (NF-κB)信号通路、肿瘤坏死因子(TNF)信号通路等多种途径发挥其治疗作用。动物实验结果表明,茯苓水提物能显著降低糖尿病大鼠的血糖和血脂水平,调节肠道菌群。主要感染类群为g_Escherichia-Shigella、g_Corynebacterium、g_Prevotella_9、g_Prevotellaceae_UCG-001和g_bacterodota_unclassified。此外,茯苓水提液降低d -乳酸和脂多糖水平,减轻结肠黏膜损伤,显著下调nod样受体pyrin - domains containing protein 3(NLRP3)、NF-κB和TNF-α蛋白水平,显著上调糖尿病发病率中occludens小带1和occludin蛋白水平。茯苓水提物可能通过修复肠道菌群紊乱、保护肠道屏障功能、抑制NF-κB/NLRP3信号通路等途径发挥治疗糖尿病的作用。研究结果为茯苓的临床应用和扩大适应症提供了科学依据。
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
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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