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体内抗溃疡活性、多酚丰富部位的植物化学研究与分子模拟圣蓟提取物。

In vivo antiulcer activity, phytochemical exploration, and molecular modelling of the polyphenolic-rich fraction of Crepis sancta extract.

机构信息

Institute of Pharmaceutical Biology and Biotechnology, Heinrich-Heine University, 40225, Düsseldorf, Germany.

Department of Pharmacognosy, Faculty of Pharmacy, Ain-Shams University, Abbasia, Cairo, 11566, Egypt.

出版信息

Inflammopharmacology. 2020 Feb;28(1):321-331. doi: 10.1007/s10787-019-00637-x. Epub 2019 Sep 3.

Abstract

Bioactivity-guided investigation of the methanol extract of Crepis sancta aerial parts, collected off Al-Tafilah, South Jordan, was applied, and in this study, the extract was explored for its phytochemical components and in vivo antiulcer activity. In addition, a docking study involving the purified compounds with the newly crystalized gastric proton pump (PDB # 5YLU) was performed. In-depth phytochemical investigation using the state-of-the-art chromatographic and analytical techniques was implemented resulting in the identification of two eudesmane-type sesquiterpenoids, 3-oxo-γ-costic acid (1) and its methyl ester (2) together with seven different methoxylated flavonols (3-9) as the extract's major components. The in vivo antiulcer study at three different doses (50, 100, and 200 mg/kg) against ethanol-induced gastric ulcer in male albino rats, compared to omeprazole (20 mg/kg) as a standard proton pump inhibitor antiulcer drug, revealed that the tested extract, at the middle and the highest doses, featured comparable or even superior activities relative to omeprazole as deduced from histopathological examination, in particular with regard to reducing inflammatory cell infiltration and ceasing mucosal haemorrhage. The tested extract revealed also a dose-dependent reduction in the volume and titrable acidity of the gastric juice together with a dose-dependent increase in the protective gastric mucin content which may explain the noticeable gastroprotective effect. Molecular modelling study of the isolated compounds showed a binding mode similar to the co-crystallized substrate vonoprazan in 5YLU which strengthens the importance of the tested extract as a potential natural remedy for treating gastric ulcer.

摘要

采用生物活性导向法,对产自约旦南部塔菲拉省的川西千里光地上部分的甲醇提取物进行了研究,旨在探索其化学成分和体内抗溃疡活性。此外,还对纯化后的化合物与新结晶的胃质子泵(PDB # 5YLU)进行了对接研究。利用最先进的色谱和分析技术进行深入的植物化学研究,鉴定出两种艾里莫芬烷型倍半萜,3-氧代-γ-环大牻牛儿酸(1)及其甲酯(2),以及七种不同的甲氧基化黄酮醇(3-9),它们是提取物的主要成分。在雄性白化大鼠中,进行了三种不同剂量(50、100 和 200mg/kg)的体内抗溃疡研究,与奥美拉唑(20mg/kg)作为标准质子泵抑制剂抗溃疡药物相比,结果表明,在中剂量和高剂量下,与奥美拉唑相比,该提取物表现出相似或甚至更优的活性,这可以从组织病理学检查中推断出来,特别是在减少炎症细胞浸润和停止粘膜出血方面。该提取物还显示出剂量依赖性地减少胃液的体积和可滴定酸度,以及剂量依赖性地增加保护性胃粘蛋白含量,这可以解释其明显的胃保护作用。对分离化合物的分子建模研究表明,结合模式类似于 5YLU 中共同结晶的底物沃诺拉赞,这增强了该提取物作为治疗胃溃疡的潜在天然药物的重要性。

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