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Phloretin Protects Bovine Rumen Epithelial Cells from LPS-Induced Injury

Lipopolysaccharide (LPS) is an endotoxin that induces immune and inflammatory responses in the rumen epithelium of dairy cows. It is well-known that flavonoid phloretin (PT) exhibits anti-oxidative, anti-inflammatory and antibacterial activity. The aim of this research was to explore whether PT coul...

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Autores principales: Wang, Kexin, Lei, Qian, Ma, Huimin, Jiang, Maocheng, Yang, Tianyu, Ma, Qianbo, Datsomor, Osmond, Zhan, Kang, Zhao, Guoqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9147548/
https://www.ncbi.nlm.nih.gov/pubmed/35622584
http://dx.doi.org/10.3390/toxins14050337
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author Wang, Kexin
Lei, Qian
Ma, Huimin
Jiang, Maocheng
Yang, Tianyu
Ma, Qianbo
Datsomor, Osmond
Zhan, Kang
Zhao, Guoqi
author_facet Wang, Kexin
Lei, Qian
Ma, Huimin
Jiang, Maocheng
Yang, Tianyu
Ma, Qianbo
Datsomor, Osmond
Zhan, Kang
Zhao, Guoqi
author_sort Wang, Kexin
collection PubMed
description Lipopolysaccharide (LPS) is an endotoxin that induces immune and inflammatory responses in the rumen epithelium of dairy cows. It is well-known that flavonoid phloretin (PT) exhibits anti-oxidative, anti-inflammatory and antibacterial activity. The aim of this research was to explore whether PT could decrease LPS-induced damage to bovine rumen epithelial cells (BRECs) and its molecular mechanisms of potential protective efficacy. BRECs were pretreated with PT for 2 h and then stimulated with LPS for the assessment of various response indicators. The results showed that 100 µM PT had no significant effect on the viability of 10 µg/mL LPS-induced BRECs, and this dose was used in follow-up studies. The results showed that PT pre-relieved the decline in LPS-induced antioxidant indicators (T-AOC and GSH-PX). PT pretreatment resulted in decreased interleukin-1β (IL-1β), IL-6, IL-8, tumor necrosis factor-α (TNF-α) and chemokines (CCL2, CCL5, CCL20) expression. The underlying mechanisms explored reveal that PT may contribute to inflammatory responses by regulating Toll-like receptor 4 (TLR4), nuclear transcription factor-κB p65 (NF-κB p65), and ERK1/2 (p42/44) signaling pathways. Moreover, further studies found that LPS-induced BRECs showed decreased expression of claudin-related genes (ZO-1, Occludin); these were attenuated by pretreatment with PT. These results suggest that PT enhances the antioxidant properties of BRECs during inflammation, reduces gene expression of pro-inflammatory cytokines and chemokines, and enhances barrier function. Overall, the results suggest that PT (at least in vitro) offers some protective effect against LPS-induced ruminal epithelial inflammation. Further in vivo studies should be conducted to identify strategies for the prevention and amelioration of short acute rumen acidosis (SARA) in dairy cows using PT.
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spelling pubmed-91475482022-05-29 Phloretin Protects Bovine Rumen Epithelial Cells from LPS-Induced Injury Wang, Kexin Lei, Qian Ma, Huimin Jiang, Maocheng Yang, Tianyu Ma, Qianbo Datsomor, Osmond Zhan, Kang Zhao, Guoqi Toxins (Basel) Article Lipopolysaccharide (LPS) is an endotoxin that induces immune and inflammatory responses in the rumen epithelium of dairy cows. It is well-known that flavonoid phloretin (PT) exhibits anti-oxidative, anti-inflammatory and antibacterial activity. The aim of this research was to explore whether PT could decrease LPS-induced damage to bovine rumen epithelial cells (BRECs) and its molecular mechanisms of potential protective efficacy. BRECs were pretreated with PT for 2 h and then stimulated with LPS for the assessment of various response indicators. The results showed that 100 µM PT had no significant effect on the viability of 10 µg/mL LPS-induced BRECs, and this dose was used in follow-up studies. The results showed that PT pre-relieved the decline in LPS-induced antioxidant indicators (T-AOC and GSH-PX). PT pretreatment resulted in decreased interleukin-1β (IL-1β), IL-6, IL-8, tumor necrosis factor-α (TNF-α) and chemokines (CCL2, CCL5, CCL20) expression. The underlying mechanisms explored reveal that PT may contribute to inflammatory responses by regulating Toll-like receptor 4 (TLR4), nuclear transcription factor-κB p65 (NF-κB p65), and ERK1/2 (p42/44) signaling pathways. Moreover, further studies found that LPS-induced BRECs showed decreased expression of claudin-related genes (ZO-1, Occludin); these were attenuated by pretreatment with PT. These results suggest that PT enhances the antioxidant properties of BRECs during inflammation, reduces gene expression of pro-inflammatory cytokines and chemokines, and enhances barrier function. Overall, the results suggest that PT (at least in vitro) offers some protective effect against LPS-induced ruminal epithelial inflammation. Further in vivo studies should be conducted to identify strategies for the prevention and amelioration of short acute rumen acidosis (SARA) in dairy cows using PT. MDPI 2022-05-11 /pmc/articles/PMC9147548/ /pubmed/35622584 http://dx.doi.org/10.3390/toxins14050337 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Kexin
Lei, Qian
Ma, Huimin
Jiang, Maocheng
Yang, Tianyu
Ma, Qianbo
Datsomor, Osmond
Zhan, Kang
Zhao, Guoqi
Phloretin Protects Bovine Rumen Epithelial Cells from LPS-Induced Injury
title Phloretin Protects Bovine Rumen Epithelial Cells from LPS-Induced Injury
title_full Phloretin Protects Bovine Rumen Epithelial Cells from LPS-Induced Injury
title_fullStr Phloretin Protects Bovine Rumen Epithelial Cells from LPS-Induced Injury
title_full_unstemmed Phloretin Protects Bovine Rumen Epithelial Cells from LPS-Induced Injury
title_short Phloretin Protects Bovine Rumen Epithelial Cells from LPS-Induced Injury
title_sort phloretin protects bovine rumen epithelial cells from lps-induced injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9147548/
https://www.ncbi.nlm.nih.gov/pubmed/35622584
http://dx.doi.org/10.3390/toxins14050337
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