Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University, Wuhan, China.
J Nutr. 2012 Nov;142(11):2017-24. doi: 10.3945/jn.112.164947. Epub 2012 Sep 26.
Long-chain (n-3) PUFA exert beneficial effects on inflammatory bowel diseases in animal models and clinical trials. In addition, pattern recognition receptors such as toll-like receptors (TLR) and nucleotide-binding oligomerization domain proteins (NOD) play a critical role in intestinal inflammation. We hypothesized that fish oil could alleviate Escherichia coli LPS-induced intestinal injury via modulation of TLR4 and NOD signaling pathways. Twenty-four weaned piglets were used in a 2 × 2 factorial design and the main factors included a dietary treatment (5% corn oil or 5% fish oil) and immunological challenge (LPS or saline). After feeding fish oil or corn oil diets for 21 d, pigs were injected with LPS or saline. At 4 h postinjection, blood samples were collected and pigs were killed. EPA, DHA, and total (n-3) PUFA were enriched in intestinal mucosa through fish supplementation. Fish oil improved intestinal morphology, indicated by greater villus height and villus height:crypt depth ratio, and intestinal barrier function, indicated by decreased plasma diamine oxidase (DAO) activity and increased mucosal DAO activity as well as enhanced protein expression of intestinal tight junction proteins including occludin and claudin-1. Moreover, fish oil decreased intestinal TNFα and PGE(2) concentrations and caspase-3 and heat shock protein 70 protein expression. Finally, fish oil downregulated the mRNA expression of intestinal TLR4 and its downstream signals myeloid differentiation factor 88, IL-1 receptor-associated kinase 1, TNFα receptor-associated factor 6, and NOD2, and its adaptor molecule, receptor-interacting serine/threonine-protein kinase 2. Fish oil decreased the protein expression of intestinal NFκB p65. These results indicate that fish oil supplementation is associated with inhibition of TLR4 and NOD2 signaling pathways and concomitant improvement of intestinal integrity under an inflammatory condition.
长链(n-3)多不饱和脂肪酸对动物模型和临床试验中的炎症性肠病有有益作用。此外,模式识别受体,如 Toll 样受体(TLR)和核苷酸结合寡聚化结构域蛋白(NOD),在肠道炎症中发挥关键作用。我们假设鱼油可以通过调节 TLR4 和 NOD 信号通路来减轻大肠杆菌 LPS 诱导的肠道损伤。采用 2×2 析因设计,使用 24 头断奶仔猪,主要因素包括饮食处理(5%玉米油或 5%鱼油)和免疫挑战(LPS 或生理盐水)。在饲喂鱼油或玉米油饮食 21 天后,猪被注射 LPS 或生理盐水。注射后 4 小时,采集血液样本并杀死猪。通过补充鱼油,肠黏膜中 EPA、DHA 和总(n-3)PUFA 得到富集。鱼油改善了肠道形态,表现为绒毛高度和绒毛高度:隐窝深度比值增加,肠道屏障功能增强,表现为血浆二胺氧化酶(DAO)活性降低,黏膜 DAO 活性增加,以及肠紧密连接蛋白包括闭合蛋白和 Claudin-1 的蛋白表达增强。此外,鱼油降低了肠道 TNFα 和 PGE2 浓度以及 caspase-3 和热休克蛋白 70 蛋白表达。最后,鱼油下调了肠道 TLR4 及其下游信号髓样分化因子 88、IL-1 受体相关激酶 1、TNFα 受体相关因子 6 和 NOD2 及其衔接分子受体相互作用丝氨酸/苏氨酸蛋白激酶 2 的 mRNA 表达。鱼油降低了肠道 NFκB p65 的蛋白表达。这些结果表明,鱼油补充与抑制 TLR4 和 NOD2 信号通路有关,并在炎症状态下改善肠道完整性。