College of Animal Sciences & Technology/College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.
Front Immunol. 2021 Sep 17;12:696148. doi: 10.3389/fimmu.2021.696148. eCollection 2021.
As the first line of defense against intestinal bacteria and toxins, intestinal epithelial cells are always exposed to bacteria or lipopolysaccharide (LPS), whereas pathogenic bacteria or LPS can cause intestinal epithelial cell damage. Previous studies have shown that konjac mannan oligosaccharides (KMOS) have a positive effect on maintaining intestinal integrity, and (BS) can promote the barrier effect of the intestine. However, it is still unknown whether KMOS and BS have a synergistic protective effect on the intestines. In this study, we used the LPS-induced Caco-2 cell injury model and mouse intestinal injury model to study the synergistic effects of KMOS and BS. Compared with KMOS or BS alone, co-treatment with KMOS and BS significantly enhanced the activity and antioxidant capacity of Caco-2 cell, protected mouse liver and ileum from LPS-induced oxidative damage, and repaired tight junction and mucus barrier damage by up-regulating the expression of Claudin-1, ZO-1 and MUC-2. Our results demonstrate that the combination of KMOS and BS has a synergistic repair effect on inflammatory and oxidative damage of Caco-2 cells and aIIeviates LPS-induced acute intestinal injury in mice.
作为抵御肠道细菌和毒素的第一道防线,肠上皮细胞经常暴露于细菌或脂多糖(LPS)中,而致病菌或 LPS 可导致肠上皮细胞损伤。先前的研究表明,魔芋甘露寡糖(KMOS)对维持肠道完整性具有积极作用,而(BS)可促进肠道的屏障作用。然而,KMOS 和 BS 对肠道是否具有协同保护作用仍不清楚。在这项研究中,我们使用 LPS 诱导的 Caco-2 细胞损伤模型和小鼠肠道损伤模型来研究 KMOS 和 BS 的协同作用。与 KMOS 或 BS 单独处理相比,KMOS 和 BS 的联合处理显著增强了 Caco-2 细胞的活性和抗氧化能力,保护了 LPS 诱导的氧化损伤的小鼠肝脏和回肠,并通过上调 Claudin-1、ZO-1 和 MUC-2 的表达修复紧密连接和粘液屏障损伤。我们的结果表明,KMOS 和 BS 的联合使用对 Caco-2 细胞的炎症和氧化损伤具有协同修复作用,并减轻 LPS 诱导的小鼠急性肠道损伤。