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葎草衍生的丙烯基酚对 TNF-α 诱导的肠道上皮细胞屏障功能障碍的影响。

Effect of Hops Derived Prenylated Phenols on TNF-α Induced Barrier Dysfunction in Intestinal Epithelial Cells.

机构信息

Institute for Pharma Technology, School of Life Sciences, University of Applied Sciences Northwestern Switzerland , Gruendenstrasse 40, 4132 Muttenz, Switzerland.

Hochschule Weihenstephan Triesdorf, University of Applied Sciences , Schulgasse 16, 94315 Straubing, Germany.

出版信息

J Nat Prod. 2017 Apr 28;80(4):925-931. doi: 10.1021/acs.jnatprod.6b00869. Epub 2017 Feb 24.

Abstract

For the prenylated hops phenols 6- and 8-prenylnaringenin (1 and 2), xanthohumol (3), and isoxanthohumol (4), a variety of biological activities has been described. In the current study, a transwell based in vitro model using the human intestinal epithelial cell line Caco-2 was developed to assess potential beneficial effects of compounds 1-4 on TNF-α-induced impairment of tight junction (TJ) permeability. Transepithelial electrical resistance (TEER) was measured using the latest cellZScope online monitoring device. TNF-α treatment (25 ng/mL) induced a significant decrease in TEER values (204.71 ± 4.57 at 72 h) compared to that in control values (245.94 ± 1.68 at 72 h). To determine preventive effects on TNF-α-induced impairment of TJ permeability, 1-4 were added to the apical compartment of Caco-2 monolayers 1 h before TNF-α treatment; afterward, TNF-α was added to the basolateral compartment to induce TJ dysfunction and incubated for a further 72 h. Using this setting, only 1 and 2 prevented epithelial disruption induced by TNF-α. To evaluate restorative effects of 1-4, TNF-α was added to the basolateral compartment of Caco-2 cell monolayers. After 48 h of incubation, 1-4 were added to the apical side, and TEER values were monitored online for a further 72 h. Under these experimental conditions, only 2 restored TNF-α induced barrier dysfunction.

摘要

对于被侧链二萜化的啤酒花酚类化合物 6-和 8-二烯丙基柚皮素(1 和 2)、黄腐酚(3)和异黄腐酚(4),已经描述了多种生物活性。在本研究中,开发了一种基于 Transwell 的体外模型,使用人肠上皮细胞系 Caco-2,以评估化合物 1-4 对 TNF-α 诱导的紧密连接(TJ)通透性损伤的潜在有益作用。使用最新的 cellZScope 在线监测设备测量跨上皮电阻(TEER)。与对照组(72 h 时为 245.94 ± 1.68)相比,TNF-α(25 ng/mL)处理导致 TEER 值显著降低(72 h 时为 204.71 ± 4.57)。为了确定对 TNF-α 诱导的 TJ 通透性损伤的预防作用,在 TNF-α 处理前 1 h 将 1-4 添加到 Caco-2 单层的顶侧腔室中;之后,将 TNF-α添加到底侧腔室以诱导 TJ 功能障碍,并进一步孵育 72 h。在此设置下,只有 1 和 2 可预防 TNF-α诱导的上皮破坏。为了评估 1-4 的修复作用,将 TNF-α添加到 Caco-2 细胞单层的基底外侧腔室中。孵育 48 h 后,将 1-4 添加到顶侧,并且在线监测 TEER 值进一步 72 h。在这些实验条件下,只有 2 可恢复 TNF-α 诱导的屏障功能障碍。

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