Abstract | PURPOSE:
Anthocyanins are well-characterized by anti-oxidative and anti-inflammatory potentials. Peptic ulcers contribute to the development of severe gastric disorders. In the current study, the effects of blueberry anthocyanin extracts (BE) on the Helicobacter pylori lipopolysaccharide (LPS)-induced peptic epithelium injures were assessed and the associated mechanism driving the effects was explored by focusing on MAPK/NF-κB pathway. METHODS: Peptic injures were induced in a mouse model using LPS plus ligation method and then the mice were treated with BE. Then changes in gastric histology, inflammatory response, and MAPK/NF-κB axis were detected. To reveal the role of MAPK/NF-κB axis in the effects of BE, human gastric epithelial cells (HGECs) were further subjected to co-treatment of BE, LPS, and MAPK activator. RESULTS: The assays of mouse model showed that BE attenuated gastric epithelial injuries by improving epithelial structure and suppressing gastric inflammatory response, which was associated with the inhibition of MAPK/NF-κB axis. In in vitro assays, BE suppressed viability and production of cytokines, and induced apoptosis in LPS-treated HGECs. The re-activation of MAPK pathway counteracted the effects of BE by re-inducing cell viability and suppressing cell apoptosis. CONCLUSIONS: The protective effects of BE against LPS-induced injuries in mouse stomach depended on the inhibition of both MAPK pathway and the downstream NF-κB signaling.
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Authors | Chi Shu, Jinlong Tian, Xu Si, Xu Xie, Bin Li, Dongnan Li |
Journal | European journal of nutrition
(Eur J Nutr)
Vol. 61
Issue 5
Pg. 2749-2759
(Aug 2022)
ISSN: 1436-6215 [Electronic] Germany |
PMID | 35288783
(Publication Type: Journal Article)
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Copyright | © 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany. |
Chemical References |
- Anthocyanins
- Lipopolysaccharides
- NF-kappa B
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Topics |
- Animals
- Anthocyanins
(pharmacology)
- Blueberry Plants
- Epithelium
(metabolism)
- Helicobacter pylori
- Humans
- Lipopolysaccharides
(pharmacology)
- Mice
- NF-kappa B
(metabolism)
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