An arabinogalactan from Lycium barbarum attenuates DSS-induced chronic colitis in C57BL/6J mice associated with the modulation of intestinal barrier function and gut microbiota

被引:6
作者
Cao, Cui [1 ,2 ,3 ]
Zhu, Beiwei [3 ,4 ]
Liu, Zhengqi [3 ,4 ,5 ]
Wang, Xue [1 ,2 ]
Ai, Chunqing [3 ,4 ]
Gong, Guiping [2 ]
Hu, Minghua [6 ]
Huang, Linjuan [1 ,2 ]
Song, Shuang [3 ,4 ]
机构
[1] Northwest Univ, Coll Life Sci, Xian 710069, Peoples R China
[2] Northwest Univ, Coll Food Sci & Technol, Shaanxi Nat Carbohydrate Resource Engn Res Ctr, Xian 710069, Peoples R China
[3] Dalian Polytech Univ, Sch Food Sci & Technol, Natl Engn Res Ctr Seafood, Dalian 116034, Peoples R China
[4] Dalian Polytech Univ, Natl & Local Joint Engn Lab Marine Bioact Polysac, Dalian 116034, Peoples R China
[5] China Agr Univ, Coll Food Sci & Nutr Engn, Beijing Adv Innovat Ctr Food Nutr & Human Hlth, Beijing 100083, Peoples R China
[6] Infinitus China Co Ltd, Jiangmen 529156, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
CHAIN FATTY-ACIDS; BIOLOGICAL-ACTIVITIES; ULCERATIVE-COLITIS; SIGNALING PATHWAYS; MUCUS BARRIER; DIETARY FIBER; POLYSACCHARIDES; LACTOBACILLUS; FERMENTATION; INFLAMMATION;
D O I
10.1039/d1fo01200b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ulcerative colitis (UC) is an incurable chronic inflammation of the enteric tract. The aim of this study was to investigate the protective effects of arabinogalactan from Lycium barbarum on DSS-induced chronic colitis. A homogeneous arabinogalactan was isolated and purified from L. barbarum, named LBP-3, which mainly consisted of arabinose and galactose with a molar ratio of 1.00 : 0.82. LBP-3 treatment remarkably alleviated body weight loss, histopathological damage and the overproduction of pro-inflammatory cytokines and enzymes in UC mice. Additionally, the intestinal barrier integrity was partially recovered by the up-regulated expression of MUC2 and tight junction proteins. Moreover, the gut microbiota shift was reversed by LBP-3 administration by enriching potential probiotic bacteria (e.g., Ruminococcaceae) and inhibiting the proliferation of harmful bacteria (e.g., Enterobacteriaceae). Furthermore, SCFAs, as major metabolites of LBP-3 fermentation by gut microbiota, were also promoted so as to maintain relatively favorable intestinal homeostasis. Overall, our findings suggested LBP-3 from L. barbarum could be a potential therapeutic candidate against UC via improving intestinal barrier function and partially restoring gut microbiota and its metabolites.
引用
收藏
页码:9829 / 9843
页数:15
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