Sun Ruiyue, Niu Honghong, Sun Mubai, Miao Xinyu, Jin Xin, Xu Xifei, Yanping Chi, Mei Hua, Wang Jinghui, Da Li, Su Ying
Institute of Agro-Product Process, Jilin Academy of Agricultural Science, Changchun, China.
Department of Food Science and Engineering, Agricultural College, Yanbian University, Yanji, China.
J Appl Microbiol. 2022 Dec;133(6):3634-3644. doi: 10.1111/jam.15797. Epub 2022 Sep 14.
This study aimed to investigate the effects of Bacillus subtilis natto JLCC513 (JLCC513) on gut microbiota, inflammation and intestinal barrier function in high-fat-diet (HFD) rats.
Sprague-Dawley (SD) rats were fed HFD for 16 weeks, and treated with JLCC513 in 9th week. The oral administration of JLCC513 decreased body weight and reduced the inflammation level in HFD rats. Pathologically, JLCC513 prevented the detachment of ileal villus and increased the villus height in rats. Mechanistically, western blot analysis showed that the protein levels of tight junction (TJ) proteins involved in intestinal barrier function, including zonula occludens-1 (ZO-1), occludin and claudin-1, were increased after JLCC513 treatment. Meanwhile, JLCC513 treatment also decreased the protein levels of toll-like receptor 4 (TLR4), nuclear factor kappa-B (NF-κB) and NOD-like receptor protein 3 (NLRP3), indicating inhibition of the TLR4/NF-κB/NLRP3 pathway. Furthermore, faecal analysis showed that JLCC513 increased the abundance of Lactobacillus and Oscillospira and the ratio of Firmicutes/Bacteroidetes (F/B), and decreased the levels of Blautia and C_Clostridium.
JLCC513 alleviated intestinal barrier dysfunction by inhibiting TLR4/NF-κB/NLRP3 pathway and regulating gut microbiota disorders.
Our study might provide new treatment strategies for obesity and metabolic diseases.
本研究旨在探讨纳豆芽孢杆菌JLCC513(JLCC513)对高脂饮食(HFD)大鼠肠道微生物群、炎症和肠道屏障功能的影响。
将斯普拉格-道利(SD)大鼠喂饲HFD 16周,并在第9周用JLCC513进行处理。口服JLCC513可降低HFD大鼠的体重并降低炎症水平。病理检查显示,JLCC513可防止大鼠回肠绒毛脱落并增加绒毛高度。机制上,蛋白质印迹分析表明,JLCC513处理后,参与肠道屏障功能的紧密连接(TJ)蛋白的水平增加,包括闭合蛋白-1(ZO-1)、闭合蛋白和Claudin-1。同时,JLCC513处理还降低了Toll样受体4(TLR4)、核因子κB(NF-κB)和NOD样受体蛋白3(NLRP3)的蛋白质水平,表明对TLR4/NF-κB/NLRP3通路具有抑制作用。此外,粪便分析显示,JLCC513增加了乳酸杆菌属和颤螺菌属的丰度以及厚壁菌门/拟杆菌门(F/B)的比例,并降低了布劳特氏菌属和C_梭菌属的水平。
JLCC513通过抑制TLR4/NF-κB/NLRP3通路和调节肠道微生物群紊乱来减轻肠道屏障功能障碍。
我们的研究可能为肥胖和代谢性疾病提供新的治疗策略。