Okra extract alleviates lipopolysaccharide-induced inflammation response through the regulation of bile acids, the receptor-mediated pathway, and gut microbiota

被引:1
作者
Zhou, Shanshan [1 ]
Yang, Li [1 ]
Qiu, Xia [1 ]
Li, Bohui [1 ]
Hu, Liang [1 ]
Tang, Zizhong [1 ]
Li, Hua [2 ]
Li, Shanshan [1 ]
Fang, Zhengfeng [2 ]
Chen, Hong [1 ]
机构
[1] Sichuan Agr Univ, Coll Food Sci, 46 Xinkang Rd, Yaan 625014, Sichuan, Peoples R China
[2] Sichuan Agr Univ, Inst Anim Nutr, Chengdu, Peoples R China
关键词
okra extract; inflammation response; signaling pathways; gut barrier; bile acid receptors; gut microbiota; ABELMOSCHUS-ESCULENTUS; AKKERMANSIA-MUCINIPHILA; IMMUNE-RESPONSES; IN-VITRO; ENZYMES; HEALTH; TRANSPORTERS; PROTECTS; GROWTH; MUCIN;
D O I
10.1002/jsfa.13571
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
BACKGROUNDOkra contains flavonoids and vitamin C as antioxidants and it contains polysaccharides as immunomodulators. Flavonoids regulate the inflammatory response in mice and may be related to gut microbiota. This study therefore aimed to investigate the impact of okra extract (OE) on inflammation in mice and to elucidate its underlying mechanism.METHODForty male Kunming (KM) mice were categorized into four groups: the control (CON) group, the lipopolysaccharide stimulation (LPS) group, the 5 mg mL-1 OE intervention (LPS + OE) group, and the 5 mg mL-1 OE supplementation plus mixed antibiotics (LPS + OE + ABX) group.RESULTSThe results showed that, compared with the OE group, the expression of inflammatory signaling pathway genes was upregulated and gut barrier genes were inhibited in the OE + ABX group. The Fxr receptor was activated and the abundance of Akkermansia was increased after OE supplementation, whereas the effect was reversed in the OE + ABX group. Meanwhile, Fxr was correlated positively with Akkermansia.CONCLUSIONThe OE supplementation alleviated the inflammatory response in mice under LPS stimulation, accompanied by changes in gut microbiota and bile acid receptors, whereas the addition of antibiotics caused a disturbance to the gut microbiota in the OE group, thus reducing the effect of OE in alleviating the inflammatory response. (c) 2024 Society of Chemical Industry.
引用
收藏
页码:7501 / 7513
页数:13
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