首页> 美国卫生研究院文献>Mediators of Inflammation >21-O-Angeloyltheasapogenol E3 a Novel Triterpenoid Saponin from the Seeds of Tea Plants Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner
【2h】

21-O-Angeloyltheasapogenol E3 a Novel Triterpenoid Saponin from the Seeds of Tea Plants Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner

机译:21-O-Angeloyltheasapogenol E3一种来自茶树种子的新型三萜皂苷以NF-κB依赖性方式抑制巨噬细胞介导的炎症反应。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

21-O-Angeloyltheasapogenol E3 (ATS-E3) is a triterpenoid saponin recently isolated from the seeds of the tea tree Camellia sinensis (L.) O. Kuntze. ATS-E3 has several beneficial properties including anti-inflammatory, antidiabetic, antiatherosclerotic, and anticancer effects. Unlike other phenolic compounds isolated from tea plants, there are no studies reporting the pharmacological action of ATS-E3. In this study, we therefore aimed to explore the cellular and molecular inhibitory activities of ATS-E3 in macrophage-mediated inflammatory responses. ATS-E3 remarkably diminished cellular responses of macrophages such as FITC-dextran-induced phagocytic uptake, sodium nitroprusside- (SNP-) induced radical generation, and LPS-induced nitric oxide (NO) production. Analysis of its molecular activity showed that this compound significantly suppressed the expression of inducible NO synthase (iNOS), nuclear translocation of nuclear factor- (NF-) κB subunits (p50 and p65), phosphorylation of inhibitor of κB kinase (IKK), and the enzyme activity of AKT1. Taken together, the novel triterpenoid saponin compound ATS-E3 contributes to the beneficial effects of tea plants by exerting anti-inflammatory and antioxidative activities in an AKT/IKK/NF-κB-dependent manner.
机译:21-O-Angeloyltheasapogenol E3(ATS-E3)是一种三萜皂苷,最近从茶树茶树(L.)O. Kuntze的种子中分离出来。 ATS-E3具有多种有益特性,包括抗炎,抗糖尿病,抗动脉粥样硬化和抗癌作用。与从茶树中分离出的其他酚类化合物不同,尚无研究报告ATS-E3的药理作用。因此,在这项研究中,我们旨在探讨ATS-E3在巨噬细胞介导的炎症反应中的细胞和分子抑制活性。 ATS-E3显着降低了巨噬细胞的细胞反应,例如FITC-葡聚糖诱导的吞噬摄取,硝普钠(SNP-)诱导的自由基生成以及LPS诱导的一氧化氮(NO)产生。对其分子活性的分析表明,该化合物显着抑制了诱导型NO合酶(iNOS)的表达,核因子-(NF-)κB亚基(p50和p65)的核易位,κB激酶(IKK)抑制剂的磷酸化和AKT1的酶活性。综上所述,新型三萜皂苷化合物ATS-E3通过以AKT / IKK /NF-κB依赖性方式发挥抗炎和抗氧化活性,从而有助于茶树的有益作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号