Suppr超能文献

从柚木中分离得到的毛蕊花糖苷通过抑制质子泵活性介导对大鼠的胃保护作用。

Verbascoside isolated from Tectona grandis mediates gastric protection in rats via inhibiting proton pump activity.

机构信息

Division of Pharmacology, Central Drug Research Institute, CSIR, Lucknow-226001, Uttar Pradesh, India.

出版信息

Fitoterapia. 2010 Oct;81(7):755-61. doi: 10.1016/j.fitote.2010.03.019. Epub 2010 Apr 11.

Abstract

Evidences have suggested that Tectona grandis (TG) attenuates gastric mucosal injury; however its mechanism has not yet been established. The aim of present study was to evaluate the gastroprotective mechanism of ethanolic extract of TG (E-EtOH), butanolic fraction (Fr-Bu) and to identify its active constituents. Anti-ulcer activities were evaluated against cold restraint (CRU) and pyloric ligation (PL) induced gastric ulcer models and further confirmed through H(+) K(+)-ATPase inhibitory activity. Cytoprotective activity was evaluated in alcohol (AL) induced gastric ulcer model and further through PGE(2) level. E-EtOH and Fr-Bu attenuated ulcer formation in CRU. Moreover E-EtOH and Fr-Bu displayed potent anti-secretory activity as evident through reduced free acidity and pepsin activity in PL, confirmed further by in vitro inhibition of H(+) K(+)-ATPase activity. In addition cytoprotective potential of E-EtOH and Fr-Bu were apparent with protection in AL model, increased PGE(2) content and enhanced mucin level in PL. Phytochemical investigations of Fr-Bu yielded terpenoides and a phenolic glycoside, verbascoside. The anti-secretory mechanism of verbascoside mediated apparently through inhibition of H(+) K(+)-ATPase with corresponding decrease in plasma gastrin level, is novel to our finding. Gastroprotection elicited by TG might be through proton pump inhibition and consequent augmentation of the defensive mechanism.

摘要

有证据表明,柚木(TG)可减轻胃黏膜损伤;但其机制尚未确定。本研究旨在评估 TG 的乙醇提取物(E-EtOH)、丁醇级分(Fr-Bu)的胃保护机制,并鉴定其活性成分。通过冷束缚(CRU)和幽门结扎(PL)诱导的胃溃疡模型评估抗溃疡活性,并通过 H(+) K(+) -ATP 酶抑制活性进一步证实。通过酒精(AL)诱导的胃溃疡模型评估细胞保护活性,并通过 PGE(2)水平进一步证实。E-EtOH 和 Fr-Bu 可减轻 CRU 中溃疡的形成。此外,E-EtOH 和 Fr-Bu 表现出有效的抗分泌活性,表现在 PL 中游离酸度和胃蛋白酶活性降低,体外 H(+) K(+) -ATP 酶活性抑制进一步证实。此外,E-EtOH 和 Fr-Bu 的细胞保护潜力在 AL 模型中表现明显,在 PL 中 PGE(2)含量增加和粘蛋白水平升高。Fr-Bu 的植物化学研究得到了萜类和酚糖苷,毛蕊花糖苷。毛蕊花糖苷介导的抗分泌机制显然是通过抑制 H(+) K(+) -ATP 酶,相应降低血浆胃泌素水平,这是我们发现的新机制。TG 引起的胃保护作用可能是通过质子泵抑制和随后增强防御机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验