CLC number: S852.4
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 2017-05-08
Cited: 1
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An Lyu, Jia-jia Chen, Hui-chuan Wang, Xiao-hong Yu, Zhi-cong Zhang, Ping Gong, Lin-shu Jiang, Feng-hua Liu. Punicalagin protects bovine endometrial epithelial cells against lipopolysaccharide-induced inflammatory injury[J]. Journal of Zhejiang University Science B, 2017, 18(6): 481-491.
@article{title="Punicalagin protects bovine endometrial epithelial cells against lipopolysaccharide-induced inflammatory injury",
author="An Lyu, Jia-jia Chen, Hui-chuan Wang, Xiao-hong Yu, Zhi-cong Zhang, Ping Gong, Lin-shu Jiang, Feng-hua Liu",
journal="Journal of Zhejiang University Science B",
volume="18",
number="6",
pages="481-491",
year="2017",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1600224"
}
%0 Journal Article
%T Punicalagin protects bovine endometrial epithelial cells against lipopolysaccharide-induced inflammatory injury
%A An Lyu
%A Jia-jia Chen
%A Hui-chuan Wang
%A Xiao-hong Yu
%A Zhi-cong Zhang
%A Ping Gong
%A Lin-shu Jiang
%A Feng-hua Liu
%J Journal of Zhejiang University SCIENCE B
%V 18
%N 6
%P 481-491
%@ 1673-1581
%D 2017
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1600224
TY - JOUR
T1 - Punicalagin protects bovine endometrial epithelial cells against lipopolysaccharide-induced inflammatory injury
A1 - An Lyu
A1 - Jia-jia Chen
A1 - Hui-chuan Wang
A1 - Xiao-hong Yu
A1 - Zhi-cong Zhang
A1 - Ping Gong
A1 - Lin-shu Jiang
A1 - Feng-hua Liu
J0 - Journal of Zhejiang University Science B
VL - 18
IS - 6
SP - 481
EP - 491
%@ 1673-1581
Y1 - 2017
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B1600224
Abstract: Objective: Bovine endometritis is one of the most common reproductive disorders in cattle. The aim of this study was to investigate the anti-inflammation potential of punicalagin in lipopolysaccharide (LPS)-induced bovine endometrial epithelial cells (bEECs) and to uncover the underlying mechanisms. Methods: bEECs were stimulated with different concentrations (1, 10, 30, 50, and 100 μg/ml) of LPS for 3, 6, 9, 12, and 18 h. MTT assay was used to assess cell viability and to identify the conditions for inflammatory injury and effective concentrations of punicalagin. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to assess gene expression of pro-inflammatory cytokines. Western blotting was used to assess levels of inflammation-related proteins. Results: Treatment of bEECs with 30 µg/ml LPS for 12 h induced cell injury and reduced cell viability. punicalagin (5, 10, or 20 µg/ml) pretreatment significantly decreased LPS-induced productions of interleukin (IL)-1β, IL-6, IL-8, and tumor necrosis factor-α (TNF-α) in bEECs. Molecular research showed that punicalagin inhibited the activation of the upstream mediator nuclear factor-κB (NF-κB) by suppressing the production of inhibitor κBα (IκBα) and phosphorylation of p65. Results also indicated that punicalagin can suppress the phosphorylation of mitogen-activated protein kinases (MAPKs) including p38, c-Jun N-terminal kinase (JNK), and extracellular signal-regulated kinase (ERK). Conclusions: punicalagin may attenuate LPS-induced inflammatory injury and provide a potential option for the treatment of dairy cows with Escherichia coli endometritis.
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