Lan Ruixia, Chang Qingqing, Wei Linlin, Zhao Zhihui
College of Coastal Agriculture Sciences, Guangdong Ocean University, Zhanjiang 524088, China.
Mar Drugs. 2021 Jan 25;19(2):57. doi: 10.3390/md19020057.
The aim of this study was to evaluate the effects of the dietary supplementation of chitosan oligosaccharides (COS) on intestinal integrity, oxidative status, and the inflammation response with hydrogen peroxide (HO) challenge. In total, 30 rats were randomly assigned to three groups with 10 replications: CON group, basal diet; AS group, basal diet + 0.1% HO in drinking water; ASC group, basal diet + 200 mg/kg COS + 0.1% HO in drinking water. The results indicated that COS upregulated ( < 0.05) villus height (VH) of the small intestine, duodenum, and ileum; mucosal glutathione peroxidase activity; jejunum and ileum mucosal total antioxidant capacity; duodenum and ileum mucosal interleukin (IL)-6 level; jejunum mucosal tumor necrosis factor (TNF)-α level; duodenum and ileum mucosal IL-10 level; the mRNA expression level of zonula occludens (ZO)-1 in the jejunum and ileum, claudin in the duodenum, nuclear factor-erythroid 2-like 2 in the jejunum, and heme oxygenase-1 in the duodenum and ileum; and the protein expression of ZO-1 and claudin in jejunum; however, it downregulated ( < 0.05) serum diamine oxidase activity and D-lactate level; small intestine mucosal malondialdehyde content; duodenum and ileum mucosal IL-6 level; jejunum mucosal TNF-α level; and the mRNA expression of IL-6 in the duodenum and jejunum, and TNF-α in the jejunum and ileum. These results suggested COS could maintain intestinal integrity under oxidative stress by modulating the intestinal oxidative status and release of inflammatory cytokines.
本研究旨在评估膳食补充壳寡糖(COS)对肠道完整性、氧化状态以及过氧化氢(HO)刺激下炎症反应的影响。总共30只大鼠被随机分为三组,每组10个重复:CON组,基础日粮;AS组,基础日粮 + 饮用水中添加0.1% HO;ASC组,基础日粮 + 饮用水中添加200 mg/kg COS + 0.1% HO。结果表明,COS上调(<0.05)小肠、十二指肠和回肠的绒毛高度(VH);黏膜谷胱甘肽过氧化物酶活性;空肠和回肠黏膜总抗氧化能力;十二指肠和回肠黏膜白细胞介素(IL)-6水平;空肠黏膜肿瘤坏死因子(TNF)-α水平;十二指肠和回肠黏膜IL-10水平;空肠和回肠中紧密连接蛋白(ZO)-1、十二指肠中claudin、空肠中核因子-红细胞2样2以及十二指肠和回肠中血红素加氧酶-1的mRNA表达水平;以及空肠中ZO-1和claudin的蛋白表达;然而,它下调(<0.05)血清二胺氧化酶活性和D-乳酸水平;小肠黏膜丙二醛含量;十二指肠和回肠黏膜IL-6水平;空肠黏膜TNF-α水平;以及十二指肠和空肠中IL-6、空肠和回肠中TNF-α的mRNA表达。这些结果表明,COS可通过调节肠道氧化状态和炎症细胞因子的释放来维持氧化应激下的肠道完整性。