Key Laboratory of Animal Diseases and Environmental Hazards of Sichuan Province, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Toxins (Basel). 2021 Sep 15;13(9):651. doi: 10.3390/toxins13090651.
The aim of this study was to investigate the effects of on the intestines morphology and integrity in rat. Rats were randomly divided into two groups and were fed with 10 g/100 g body weight (BW) basal diet and 10 g/100 g BW experimental diet, which was a mixture of powder and basal diet in a 3:7 ratio. The feeding experiment lasted for 60 days. At days 28 and 60 of the experiment, eight rats/group/timepoint were randomly selected, weighed, and sacrificed, then blood and intestinal tissues were collected and stored for further analysis. The results showed that caused pathological changes and injury in the intestine, elevated serum diamine oxidase (DAO), D-lactate (D-LA), and secretory immunoglobulin A (sIgA) levels, reduced occludin levels in intestinal tissues, as well as increased the count of intraepithelial leukocytes (IELs) and lamina propria leukocytes (LPLs) in the intestine ( < 0.05 or < 0.01). In addition, the mRNA and protein (ELISA) expressions of pro-inflammation cytokines (IL-1β, IL-2, TNF-α, and IFN-ϒ) were elevated in the treatment groups, whereas anti-inflammatory cytokines such as IL-4 and IL-10 were reduced ( < 0.01 or < 0.05). Therefore, the results obtained in this study indicated that impaired intestinal function in rats by damaging the intestine structure and integrity, and also triggered an inflammation immune response that led to intestinal immune barrier dysfunction.
本研究旨在探讨 对大鼠肠道形态和完整性的影响。大鼠随机分为两组,分别喂食 10 g/100 g 体重(BW)基础饲料和 10 g/100 g BW 实验饲料,后者是 粉与基础饲料以 3:7 的比例混合而成。喂养实验持续 60 天。在实验的第 28 天和第 60 天,每组随机选择 8 只大鼠/时间点,称重并处死,然后收集和储存血液和肠道组织以备进一步分析。结果表明, 导致肠道发生病理变化和损伤,血清二胺氧化酶(DAO)、D-乳酸(D-LA)和分泌型免疫球蛋白 A(sIgA)水平升高,肠道组织中紧密连接蛋白(occludin)水平降低,上皮内白细胞(IELs)和固有层白细胞(LPLs)计数增加(<0.05 或 <0.01)。此外,炎症细胞因子(IL-1β、IL-2、TNF-α 和 IFN-ϒ)的 mRNA 和蛋白(ELISA)表达在 处理组中升高,而抗炎细胞因子如 IL-4 和 IL-10 则降低(<0.01 或 <0.05)。因此,本研究结果表明, 通过破坏肠道结构和完整性,损害大鼠肠道功能,并引发炎症免疫反应,导致肠道免疫屏障功能障碍。