Macrophage activation by an acidic polysaccharide isolated from Angelica sinensis (Oliv.) Diels.

Xingbin Yang, Yan Zhao, Haifang Wang, Qibing Mei
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引用次数: 54

Abstract

This study was designed to identify and characterize the mechanism of macrophage activation by AAP, an acidic polysaccharide fraction isolated from the roots of Angelica sinensis (Oliv.) Diels. As a result, AAP significantly enhanced nitric oxide (NO) production and cellular lysosomal enzyme activity in murine peritoneal macrophages in vitro and in vivo. Furthermore, L-NAME, a specific inhibitor of inducible nitric oxide synthase (iNOS), effectively suppressed AAP-induced NO generation in macrophages, indicating that AAP stimulated macrophages to produce NO through the induction of iNOS gene expression and the result was further confirmed by the experiment of the increase of AAPinduced iNOS transcription in a dose-dependent manner. To further investigate, AAP was shown to strongly augment toll-like receptor 4 (TLR4) mRNA expression and the pretreatment of macrophages with anti-TLR4 antibody significantly blocked AAP-induced NO release and the increase of iNOS activity, and tumor necrosis factor-alpha (TNF-alpha) secretion.

当归酸性多糖对巨噬细胞的激活作用一昼夜的。
本研究旨在鉴定和表征从当归根中提取的酸性多糖AAP活化巨噬细胞的机制。一昼夜的。结果表明,AAP可显著提高小鼠腹膜巨噬细胞一氧化氮(NO)的生成和细胞溶酶体酶活性。此外,诱导型一氧化氮合酶(inducible nitric oxide synthase, iNOS)特异性抑制剂L-NAME可有效抑制AAP诱导的巨噬细胞NO生成,说明AAP通过诱导iNOS基因表达刺激巨噬细胞产生NO, AAP诱导的iNOS转录增加呈剂量依赖性的实验进一步证实了这一结果。进一步研究发现,AAP可增强toll样受体4 (TLR4) mRNA的表达,抗TLR4抗体预处理巨噬细胞可显著阻断AAP诱导的NO释放、iNOS活性增加和肿瘤坏死因子- α (tnf - α)分泌。
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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