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Effects of phytogenic feed additives on cellular oxidative stress and inflammatory reactions in intestinal porcine epithelial cells

机译:植物性饲料添加剂对猪上皮细胞氧化应激及炎症反应的影响

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摘要

Due to increasing concerns about the use of antibiotic growth promoters (>AGP) in livestock production and their complete ban in the European Union in 2006, suitable alternatives are urgently needed. Among others, anti-inflammatory activities of AGP are discussed as their putative mode of action. As numerous phytochemicals are known to modulate the cellular antioxidant capacity and immune response, we studied the antioxidative and anti-inflammatory properties of a phytogenic (plant-derived) feed additive (>PFA) in intestinal porcine epithelial cells (>IPEC-J2). The effects of the PFA were compared with those of selected phytogenic ingredients (grape seed extract [>GRS], licorice extract [>LIC], menthol [>MENT], methyl salicylate [>MES], oak bark extract [>OAK], oregano essential oil [>ORE], and a plant powder mix [>PLA]), and with the effects of the AGP tylosin (>TYL). Oxidative or inflammatory stress was induced by stimulating IPEC-J2 with hydrogen peroxide (>H>2>O>2; 0.5 mM) or tumor necrosis factor alpha (>TNF-α; 10 ng/mL), respectively. The antioxidative effects of feed additives were assessed with a reactive oxygen species (>ROS)-sensitive probe and by measuring the expression of 6 antioxidative target genes via quantitative real-time PCR (>RT-qPCR). Anti-inflammatory potential was analyzed using a nuclear factor kappa-light-chain-enhancer of activated B cells (>NF-κB) reporter gene assay. Moreover, the expression levels of 6 NF-κB target genes were measured using RT-qPCR analysis, and the release of IL-6 was analyzed via ELISA. Significant decreases in cellular ROS upon H2O2 treatment were observed for the PFA (P < 0.001), LIC (P < 0.001), ORE (P < 0.05), and GRS (P < 0.01). No significant changes in the expression of antioxidative genes were found. NF-κB activation upon TNF-α treatment was significantly inhibited by the PFA (P < 0.05) and by ORE (P < 0.001). Moreover, the PFA and ORE significantly reduced the gene expression of IL-6 (P < 0.001), IL-8 (P < 0.001), and C-C motif chemokine ligand 2 (>CCL2; P < 0.05), as well as the release of IL-6 (P < 0.05). The other phytogenic compounds as well as the AGP TYL did not significantly affect any of the inflammatory parameters. In summary, we revealed the antioxidative properties of the PFA, LIC, ORE, and GRS, as well as anti-inflammatory properties of the PFA and ORE in IPEC-J2, providing a better understanding of the mode of action of this PFA under our experimental conditions.
机译:由于人们越来越担心在牲畜生产中使用抗生素生长促进剂(> AGP )及其在2006年被欧盟完全禁止,因此迫切需要合适的替代品。其中,AGP的抗炎活性被认为是其公认的作用方式。由于已知许多植物化学物质可调节细胞的抗氧化能力和免疫反应,因此我们研究了肠道猪上皮细胞(植物源性)饲料添加剂(> PFA )的抗氧化和抗炎特性。 > IPEC-J2 )。将PFA的效果与选定的植物成分进行比较(葡萄籽提取物[> GRS ],甘草提取物[> LIC ],薄荷醇[> MENT >],水杨酸甲酯[> MES ],橡树皮提取物[> Oak ],牛至精油[> ORE ]和植物粉末混合物[ > PLA ]),并具有AGP泰乐菌素(> TYL )的作用。通过用过氧化氢(> H > 2 > O > 2 ; 0.5 mM)刺激IPEC-J2诱导氧化性或炎症性应激)或肿瘤坏死因子α(>TNF-α; 10 ng / mL)。使用活性氧(> ROS )敏感探针评估饲料添加剂的抗氧化作用,并通过定量实时PCR(> RT-qPCR < / strong>)。使用激活的B细胞的核因子κ轻链增强子(>NF-κB)报告基因分析来分析抗炎潜力。此外,使用RT-qPCR分析测量了6个NF-κB靶基因的表达水平,并通过ELISA分析了IL-6的释放。 PFA(P <0.001),LIC(P <0.001),ORE(P <0.05)和GRS(P <0.01)观察到H2O2处理后细胞ROS的显着降低。没有发现抗氧化基因表达的显着变化。 PFA(P <0.05)和ORE(P <0.001)显着抑制了TNF-α处理后的NF-κB活化。而且,PFA和ORE显着降低IL-6(P <0.001),IL-8(P <0.001)和CC基序趋化因子配体2(> CCL2 ; P <0.05)的基因表达。以及IL-6的释放(P <0.05)。其他植物性化合物以及AGP TYL均未显着影响任何炎症参数。总而言之,我们在IPEC-J2中揭示了PFA,LIC,ORE和GRS的抗氧化特性,以及PFA和ORE的抗炎特性,从而使我们更好地理解了该PFA在我们的作用下的作用方式。实验条件。

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