Wang Na, Han Qing, Wang Gai, Ma Wei-Ping, Wang Jia, Wu Wen-Xin, Guo Yu, Liu Li, Jiang Xiao-Yu, Xie Xiao-Li, Jiang Hui-Qing
Department of Gastroenterology, The Second Hospital of Hebei Medical University, Hebei Key Laboratory of Gastroenterology, Hebei Medical University, Hebei Institute of Gastroenterology, No. 215 Heping West Road, Shijiazhuang, 050000, Hebei, China.
Pediatric Intensive Care Unit, Baoding Children's Hospital, Baoding, Hebei, China.
Dig Dis Sci. 2016 Sep;61(9):2522-34. doi: 10.1007/s10620-016-4184-4. Epub 2016 May 4.
BACKGROUND/AIM: Obstructive jaundice (OJ) is frequently complicated by infections and has been associated with increased bacterial translocation, intestinal epithelial hyperpermeability, and oxidative stress, but the mechanism remains unclear. The potential effect of resveratrol (Res) on modifying intestinal epithelial dysfunction was evaluated both in vitro and in vivo.
Caco-2 cells (in vitro) and male Wistar rats (n = 60; in vivo) were used to evaluate the role of Res on intestinal epithelial dysfunction. Hydrogen peroxide was used to induce oxidative stress in the Caco-2 cells. In bile duct-ligated group, OJ was successfully established on Day 7 after bile duct ligation, whereas sham-operated and vehicle-treated rats served as controls. Western blot and RT-qPCR were performed to analyze TJ proteins expression in epithelium isolated from rat intestine.
Intestinal hyperpermeability was associated with decreased expression and phosphorylation of occludin and zonula occluden (ZO-1), but increased oxidation in Caco-2 cells and the intestinal epithelium. Res treatment increased the epithelial expression and phosphorylation of occludin and ZO-1 in a concentration-dependent manner. Moreover, Res which protected Caco-2 cells from H2O2-induced oxidative damage clearly reduced malondialdehyde level and intracellular reactive oxygen species accumulation, but increased the expression levels of superoxide dismutase and heme oxygenase-1 (HO-1). Further studies showed that Res also inhibited H2O2-induced protein kinase C activity and p38 phosphorylation. Interestingly, these effects of Res were abolished by the HO-1 inhibitor zinc protoporphyrin or knockdown of HO-1 by siRNA.
Res protected gut barrier function possibly by initiating HO-1-dependent signaling which is essential for common expression of key tight junction proteins. It also provides a rationale to develop Res clinical applications of intestinal disorders.
背景/目的:梗阻性黄疸(OJ)常并发感染,与细菌易位增加、肠上皮通透性增高及氧化应激有关,但其机制尚不清楚。本研究在体外和体内评估了白藜芦醇(Res)对改善肠上皮功能障碍的潜在作用。
采用Caco-2细胞(体外)和雄性Wistar大鼠(n = 60;体内)评估Res对肠上皮功能障碍的作用。用过氧化氢诱导Caco-2细胞氧化应激。在胆管结扎组,胆管结扎后第7天成功建立OJ模型,假手术组和溶剂处理组大鼠作为对照。采用蛋白质免疫印迹法和实时定量聚合酶链反应分析大鼠肠上皮中紧密连接蛋白的表达。
肠通透性增高与闭合蛋白和闭锁小带蛋白(ZO-1)表达及磷酸化水平降低有关,但Caco-2细胞和肠上皮氧化增加。Res处理以浓度依赖方式增加了闭合蛋白和ZO-1的上皮表达及磷酸化。此外,Res保护Caco-2细胞免受H2O2诱导的氧化损伤,明显降低丙二醛水平和细胞内活性氧积累,但增加了超氧化物歧化酶和血红素加氧酶-1(HO-1)的表达水平。进一步研究表明,Res还抑制H2O2诱导的蛋白激酶C活性和p38磷酸化。有趣的是,HO-1抑制剂锌原卟啉或小干扰RNA敲低HO-1可消除Res的这些作用。
Res可能通过启动HO-1依赖的信号传导保护肠道屏障功能,这对关键紧密连接蛋白的共同表达至关重要。这也为Res在肠道疾病中的临床应用开发提供了理论依据。