Guangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
PLoS One. 2013 Sep 16;8(9):e73571. doi: 10.1371/journal.pone.0073571. eCollection 2013.
Dysfunction of the intestinal epithelial tight junction (TJ) barrier is known to have an important etiologic role in the pathophysiology of heat stroke. N-3 polyunsaturated fatty acids (PUFAs), including eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), play a role in maintaining and protecting the TJ structure and function. This study is aimed at investigating whether n-3 PUFAs could alleviate heat stress-induced dysfunction of intestinal tight junction.
Human intestinal epithelial Caco-2 cells were pre-incubated with EPA, DHA or arachidonic acid (AA) and then exposed to heat stress. Transepithelial electrical resistance (TEER) and Horseradish Peroxidase (HRP) permeability were measured to analyze barrier integrity. Levels of TJ proteins, including occludin, ZO-1 and claudin-2, were analyzed by Western blot and localized by immunofluorescence microscopy. Messenger RNA levels were determined by quantitative real time polymerase chain reaction (Q-PCR). TJ morphology was observed by transmission electron microscopy.
EPA effectively attenuated the decrease in TEER and impairment of intestinal permeability in HRP flux induced by heat exposure. EPA significantly elevated the expression of occludin and ZO-1, while DHA was less effective and AA was not at all effective. The distortion and redistribution of TJ proteins, and disruption of morphology were also effectively prevented by pretreatment with EPA.
This study indicates for the first time that EPA is more potent than DHA in protecting against heat-induced permeability dysfunction and epithelial barrier damage of tight junction.
已知肠道上皮紧密连接 (TJ) 屏障功能障碍在中暑的病理生理学中具有重要的病因作用。n-3 多不饱和脂肪酸 (PUFA),包括二十碳五烯酸 (EPA) 和二十二碳六烯酸 (DHA),在维持和保护 TJ 结构和功能方面发挥作用。本研究旨在探讨 n-3 PUFAs 是否可以减轻热应激引起的肠道紧密连接功能障碍。
人肠道上皮 Caco-2 细胞用 EPA、DHA 或花生四烯酸 (AA) 预孵育,然后暴露于热应激下。通过测定跨上皮电阻 (TEER) 和辣根过氧化物酶 (HRP) 通透性来分析屏障完整性。通过 Western blot 分析 TJ 蛋白(包括闭合蛋白、ZO-1 和 Claudin-2)的水平,并通过免疫荧光显微镜定位。通过定量实时聚合酶链反应 (Q-PCR) 测定信使 RNA 水平。通过透射电子显微镜观察 TJ 形态。
EPA 有效减弱了热暴露引起的 TEER 下降和 HRP 通量引起的肠道通透性损伤。EPA 显著上调了闭合蛋白和 ZO-1 的表达,而 DHA 效果较差,AA 则完全无效。TJ 蛋白的扭曲和重分布以及形态的破坏也被 EPA 的预处理有效阻止。
本研究首次表明,EPA 在保护热诱导的通透性功能障碍和紧密连接上皮屏障损伤方面比 DHA 更有效。