Proanthocyanidins and β-Glucan Synergistically Regulate Intestinal Inflammation in Dextran Sulfate Sodium-Induced Colitis Mice

被引:0
作者
Xia, Pengkui [1 ,2 ]
Li, Ruyi [1 ]
Chen, Mianhong [1 ]
Zeng, Fanke [1 ]
Zhou, Wei [1 ]
Hou, Tao [2 ]
机构
[1] Chinese Acad Trop Agr Sci, Agr Prod Proc Res Inst, Key Lab Trop Crop Prod Proc, Minist Agr & Rural Affairs, Zhanjiang 524001, Guangdong, Peoples R China
[2] Huazhong Agr Univ, Coll Food Sci & Technol, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
proanthocyanidins; beta-glucan; colitis; synergistic anti-inflammatory function; BOWEL-DISEASE; ULCERATIVE-COLITIS; DIMETHYL FUMARATE; CLINICAL-ASPECTS; MICROBIOTA; BARRIER; PERMEABILITY; PATHOGENESIS; DERIVATIVES; BENZOFURAN;
D O I
10.1021/acs.jafc.4c03544
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Proanthocyanidins (PA) have been proven to have an anti-inflammation effect in multiple models by regulating oxidative stress. beta-glucan (BG) could alleviate colitis from the perspectives of intestinal permeability and gut microbiota. In the present study, the synergistic anti-inflammatory function of PA and BG was explored from multiple aspects including immune response, intestinal barrier, gut microbiota, and differential metabolites. The results showed that the supplementation of PA and BG improved the colitis symptoms including atrophy of the colon, body weight loss, and organ index increase. Additionally, inflammatory cytokine levels and oxidative stress status were significantly regulated with the intake of PA and BG. Moreover, PA and BG intervention improved intestinal permeability and promoted the expression of barrier proteins. The microbiome and metabolic profile of cecal contents showed that PA and BG supplementation increased the abundance of anti-inflammatory bacteria and decreased the abundance of pro-inflammatory bacteria. Furthermore, some beneficial metabolites involved in amino acid metabolism, carbohydrate metabolism, and biosynthesis of other secondary metabolite pathways were increased. Overall, these findings have demonstrated the regulation of the inflammatory response and remodel of metabolite profiles by PA and BG complexes, indicating that it may serve as a new strategy for inflammatory bowel disease treatment in the future.
引用
收藏
页码:19366 / 19377
页数:12
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