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Protective Effects of Ferulic Acid against Heat Stress-Induced Intestinal Epithelial Barrier Dysfunction In Vitro and In Vivo

机译:阿魏酸对体内和体外热应激诱导的肠道上皮屏障功能障碍的保护作用

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摘要

Heat stress is important in the pathogenesis of intestinal epithelial barrier dysfunction. Ferulic acid (FA), a phenolic acid widely found in fruits and vegetables, can scavenge free radicals and activate cell stress responses. This study is aimed at investigating protective effects of FA on heat stress-induced dysfunction of the intestinal epithelial barrier in vitro and in vivo. Intestinal epithelial (IEC-6) cells were pretreated with FA for 4 h and then exposed to heat stress. Heat stress caused decreased transepithelial electrical resistance (TER) and increased permeability to 4-kDa fluorescein isothiocyanate (FITC)-dextran (FD4). Both effects were inhibited by FA in a dose-dependent manner. FA significantly attenuated the decrease in occludin, ZO-1 and E-cadherin expression observed with heat stress. The distortion and redistribution of occludin, ZO-1 and E-cadherin proteins were also effectively prevented by FA pretreatment. Moreover, heat stress diminished electron-dense material detected in tight junctions (TJs), an effect also alleviated by FA in a dose-dependent manner. In an in vivo heat stress model, FA (50 mg/kg) was administered to male Sprague–Dawley rats for 7 consecutive days prior to exposure to heat stress. FA pretreatment significantly attenuated the effects of heat stress on the small intestine, including the increased FD4 permeability, disrupted tight junctions and microvilli structure, and reduced occludin, ZO-1 and E-cadherin expression. Taken together, our results demonstrate that FA pretreatment is potentially protective against heat stress-induced intestinal epithelial barrier dysfunction.
机译:热应激在肠上皮屏障功能障碍的发病机理中很重要。阿魏酸(FA)是在水果和蔬菜中广泛发现的一种酚酸,可以清除自由基并激活细胞应激反应。这项研究的目的是在体外和体内研究FA对热应激诱导的肠上皮屏障功能障碍的保护作用。肠上皮(IEC-6)细胞用FA预处理4小时,然后暴露于热应激下。热应力导致跨上皮电阻(TER)降低和对4-kDa异硫氰酸荧光素(FITC)-葡聚糖(FD4)的渗透性增加。 FA以剂量依赖性方式抑制两种作用。 FA显着减弱了在热应激下观察到的occludin,ZO-1和E-cadherin表达的下降。 FA预处理还可以有效地阻止occludin,ZO-1和E-cadherin蛋白的变形和重新分布。此外,热应力减少了在紧密结(TJs)中检测到的电子致密材料,FA也以剂量依赖的方式减轻了这种影响。在体内热应激模型中,雄性Sprague-Dawley大鼠在暴露于热应激之前连续7天服用FA(50 mg / kg)。 FA预处理可显着减弱热应激对小肠的影响,包括增加FD4渗透性,破坏紧密连接和微绒毛结构,以及降低occludin,ZO-1和E-cadherin表达。两者合计,我们的结果表明,FA预处理可能具有抗热应激诱导的肠上皮屏障功能障碍的作用。

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