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Rosmarinic acid alleviated intestinal barrier damage caused by Escherichia coli by regulating the gut microbiota and inhibiting the NF-κB signalling pathway in mice
被引:0
|作者:
Yi, Dandan
[1
]
Liu, Xia
[1
]
Wang, Menghui
[1
]
Zhao, Linyi
[1
]
Liu, Yu
[1
]
Xu, Zhiran
[1
]
Peng, Ying
[1
]
Zhang, Rui
[1
]
Wei, Qianyin
[1
]
Liang, Zhengmin
[1
,2
,3
]
He, Jiakang
[1
,2
,3
]
机构:
[1] Guangxi Univ, Coll Anim Sci & Technol, Room 307,100 Daxue Rd, Nanning 530004, Guangxi, Peoples R China
[2] Guangxi Key Lab Anim Breeding Dis Control & Preven, Nanning 530004, Peoples R China
[3] Guangxi Zhuang Autonomous Reg Engn Res Ctr Vet Bio, Nanning 530004, Peoples R China
基金:
中国国家自然科学基金;
关键词:
D O I:
10.1039/d4fo02654c
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:
Escherichia coli (E. coli) is a common zoonotic foodborne pathogen that poses a major threat to public health and economic development. Rosmarinic acid (RA) can inhibit intestinal inflammation; however, the protective effect of RA against the intestinal barrier damage induced by E. coli in mice and the underlying mechanism have not been elucidated. In this study, mice were orally administered with RA (20 mg kg-1) by gavage for one week and then were intraperitoneally challenged with E. coli. Mouse colonic epithelial cells (MCECs) were pretreated with RA for 6 h and challenged with E. coli (MOI = 1000) for 3 h. The results revealed that RA alleviated E. coli-induced weight loss in mice; reduced the increase in the levels of TNF-alpha, IL-6 and IL-1 beta in the serum; alleviated the decrease in ZO-1 protein expression; and increased intestinal permeability by inhibiting the NF-kappa B signalling pathway both in vivo and in vitro. Moreover, RA relieved the increase in intestinal permeability, reversed the structural damage to the mouse gut microbiota caused by E. coli, and increased the abundance of beneficial bacteria, including Lachnospiraceae_NK4136_group. Additionally, RA lost its protective function against E. coli infection in a pseudosterile mouse model, suggesting that the protection induced by RA was dependent on the gut microbiota. In conclusion, these results indicate that RA alleviates E. coli-induced inflammatory damage to the intestinal barrier by inhibiting the NF-kappa B signalling pathway and maintaining gut microbiota homeostasis. These findings provide new ideas and foundations for the application of RA as protection against E. coli.
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页码:11740 / 11756
页数:17
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