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Chemical Composition and Immuno-Modulatory Effects of Urtica dioica L. (Stinging Nettle) Extracts

机译:荨麻酶二氧化硅L.(刺痛荨麻)提取物的化学成分及免疫调节作用

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The purpose of this work was to determine the chemical profile of stinging nettle and to provide an insight into the mechanisms by which it ameliorates the immune response. Qualitative and quantitative liquid chromatography tandem mass spectrometry analyses indicated that phenolic acids (5-O-caffeoylquinic acid as dominant) and flavonol glycosides (rutin, isoquercitrin, and kaempferol 3-O-glucoside) are present in the aerial parts, while lignans (secoisolariciresinol, 9,9'-bisacetyl-neo-olivil and their glucosides) were detected in the root. Herb and root extracts expressed selective inhibition toward cyclooxygenase and lipoxygenase branches in human platelets: root extracts were better at inhibiting thromboxane production, while herb extracts were more specific toward inhibition of 12-lipoxygenase pathway. Stinging nettle extracts mildly increased monocyte chemoattractant protein-1 and growth-related oncogene release from nonstimulated intestinal epithelial cells, stimulating MyD88/NF-kappa B/p38 signaling, hence preserving the epithelial integrity and enhancing intestinal steady-state defense. Additionally, root extract reduced lipopolysaccharide-induced monocyte chemoattractant protein-1/growth-related oncogene secretion and cyclooxygenase-2 expression in intestinal epithelial cells, thus showing the potential protective effect against tissue damage caused by inflammation processes. These observations suggest that stinging nettle is an interesting candidate for the development of phytopharmaceuticals or dietary supplements for cotreatment of various inflammatory diseases, particularly inflammatory bowel diseases. Copyright (C) 2017 John Wiley & Sons, Ltd.
机译:这项工作的目的是确定刺痛荨麻的化学型材,并对其改善免疫应答的机制提供了深入的洞察力。定性和定量液相色谱串联质谱分析表明,在空中部位中存在酚醛酸(5-O-咖啡算法为优势)和黄酮,异喹啉和葡萄糖3-O-葡糖苷),而木质素(Secoisolaricirsinol ,在根系中检测到9,9,9'-双乙酰基 - 新olivil及其葡糖苷)。 Herb和Root提取物表达对人血小板中的环氧氧基酶和脂氧合酶分支的选择性抑制:根提取物在抑制血栓乳糖的产生时更好,而药草提取物更具体地朝抑制12-脂氧基酶途径。从非刺激的肠上皮细胞中刺痛荨麻疹提取轻微增加的单核细胞化学蛋白-1和生长相关的癌基因释放,刺激MyD88 / NF-Kappa B / P38信号传导,因此保持上皮完整性和增强肠稳态防御。另外,根提取物降低脂多糖诱导的单核细胞趋化蛋白-1 /生长相关的癌基因分泌和在肠上皮细胞中的环氧氧酶-2表达,从而显示出对由炎症过程引起的组织损伤的潜在保护作用。这些观察结果表明,刺痛的荨麻是一种有趣的候选者,用于开发植物药物或膳食补充剂,用于各种炎症性疾病,特别是炎症性肠病。版权所有(c)2017 John Wiley&Sons,Ltd。

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