Anti-acute gastric ulcer resistance of Aurantii Fructus Immaturus juice processing Atractylodis Macrocephalae Rhizoma by regulating PTGS2, MAPK1, and KDR targets based on metabolomics and integrated network pharmacology analysis

Wanai Xu, Jingyu Wu, Danyang Yang, Yu-Xun Chen, Xiao-Ying Wu, Rou Wen, Liping Yan, Chao Li, Huan Yu
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Abstract

Abstract Background Currently, traditional methods of treating acute gastric ulcer (AGU) have many drawbacks, necessitating an alternative therapy with fewer adverse effects. Atractylodis Macrocephalae Rhizoma (BZ) is known for strengthening the spleen and harmonizing the stomach. BZ processed with Aurantii Fructus Immaturus juice (ZSZBZ), a classic decoction since the Han Dynasty, can enhance the efficacy of BZ. However, the key active components and targets of action of ZSZBZ remain undiscovered. Aim of the study This study aimed to investigate the bioactive chemical constituents of ZSZBZ against AGU and their possible mechanisms of action, elucidating the scientific content of ZSZBZ processing. Materials and methods Initially, we examined rat stomach histopathology and conducted ELISA for oxidative stress and inflammation. Subsequently, we investigated underlying mechanisms using metabolomics. Further analysis of potent components and key targets in ZSZBZ was conducted through liquid chromatography-mass spectrometry analysis combined with network pharmacology. Finally, key targets were analyzed by Western blot. Results ZSZBZ improved gastric histopathology, reversing high alcohol-induced oxidative stress (SOD, CAT) and inflammatory level (TNF-α, IL-6) disorders. This is associated with ZSZBZ’s regulation of amino acid metabolism, energy metabolism, and inflammatory response-related metabolic pathways, along with key targets PTGS2, MAPK1, and KDR. The significant increase in potency of ZSZBZ may be attributed to elevated levels of naringenin, hesperidin, hesperidin, and rhamnoceroside after concoction. Conclusions Combining metabolomics and network pharmacology, this study elucidated that ZSZBZ enhanced gastroprotection by modulating amino acid metabolism, antioxidant, and inflammation-related targets and pathways, providing insights into the bioactive compounds and potential mechanisms of herbal concoctions.
基于代谢组学和整合网络药理学分析的白术汁加工品通过调控 PTGS2、MAPK1 和 KDR 靶点抗急性胃溃疡的作用
摘要 背景 目前,治疗急性胃溃疡(AGU)的传统方法存在诸多弊端,需要一种不良反应较少的替代疗法。白术具有健脾和胃的功效。将白术与枳实汁(ZSZBZ)(汉代以来的经典煎药)一起煎煮,可增强白术的疗效。然而,ZSZBZ 的主要活性成分和作用靶点仍未被发现。研究目的 本研究旨在探讨 ZSZBZ 对 AGU 的生物活性化学成分及其可能的作用机制,阐明 ZSZBZ 加工的科学内涵。材料和方法 首先,我们检查了大鼠胃的组织病理学,并对氧化应激和炎症进行了 ELISA 检测。随后,我们利用代谢组学研究了其潜在机制。通过液相色谱-质谱分析结合网络药理学,进一步分析了 ZSZBZ 中的有效成分和关键靶点。最后,对关键靶标进行了 Western 印迹分析。结果 ZSZBZ 改善了胃组织病理学,逆转了酒精引起的氧化应激(SOD、CAT)和炎症水平(TNF-α、IL-6)紊乱。这与 ZSZBZ 对氨基酸代谢、能量代谢和炎症反应相关代谢途径以及关键靶点 PTGS2、MAPK1 和 KDR 的调节有关。柚皮苷、橙皮甙、橙皮素和鼠李糖甙在冲服后水平升高,可能是 ZSZBZ 药效明显增强的原因。结论 本研究结合代谢组学和网络药理学,阐明了 ZSZBZ 通过调节氨基酸代谢、抗氧化和炎症相关靶点和通路增强胃保护作用,为了解中药复方的生物活性化合物和潜在机制提供了见解。
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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