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黄芪多糖通过降低 LPS 感染的 Caco2 细胞的通透性来减少炎症反应。

Astragalus polysaccharide reduces inflammatory response by decreasing permeability of LPS-infected Caco2 cells.

机构信息

College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, 712100, China.

出版信息

Int J Biol Macromol. 2013 Oct;61:347-52. doi: 10.1016/j.ijbiomac.2013.07.013. Epub 2013 Aug 2.

Abstract

As the major constituent of Radix Astragali, Astragalus polysaccharide (APS) is known for its anti-inflammation and immunomodulatory functions. The objective of this study was to investigate the effect of APS on inflammatory response and structural changes in lipopolysaccharide (LPS)-infected Caco2 cells. Caco2 cells were co-cultured with APS and LPS, with APS added after the addition of LPS (post-addition), before the addition of LPS (pre-addition), or simultaneously with the addition of LPS (simultaneous addition). The mRNA expression of inflammatory indicators and tight junctions was measured by RT-qPCR. Short circuit current (Isc) was recorded by an Ussing chamber system. Addition of APS significantly down-regulated the expression of TNF-α, IL-1β and IL-8 (P<0.05) and the Isc levels (P<0.05) of LPS-infected Caco2 cells for all three administration treatments. The minimum anti-inflammatory concentration of APS was 50, 100, and 100 μg/mL for pre-, post-, and simultaneous additions of APS, respectively. The mRNA expression of zonula occludens-1 (ZO-1) and occludin was significantly up-regulated for post- and pre-additions of APS, respectively (P<0.05). Results suggested that APS had anti-inflammatory and structure protective properties for LPS-infected Caco2 cells, and may be used as a preventative treatment for intestine cells.

摘要

作为黄芪的主要成分,黄芪多糖(APS)以其抗炎和免疫调节功能而闻名。本研究旨在探讨 APS 对脂多糖(LPS)感染的 Caco2 细胞炎症反应和结构变化的影响。将 Caco2 细胞与 APS 和 LPS 共培养,APS 分别在 LPS 加入后(后加入)、加入前(前加入)或同时加入(同时加入)时添加。通过 RT-qPCR 测量炎症指标和紧密连接的 mRNA 表达。通过 Ussing 室系统记录短路电流(Isc)。APS 的添加显著下调了 LPS 感染的 Caco2 细胞中 TNF-α、IL-1β 和 IL-8 的表达(P<0.05)和 Isc 水平(P<0.05)。APS 的最小抗炎浓度分别为 LPS 感染的 Caco2 细胞前、后和同时添加 APS 的 50、100 和 100μg/mL。APS 的后和前添加分别显著上调了紧密连接蛋白-1(ZO-1)和封闭蛋白的 mRNA 表达(P<0.05)。结果表明,APS 对 LPS 感染的 Caco2 细胞具有抗炎和结构保护作用,可作为肠细胞的预防治疗药物。

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