膳食补充苯甲酸和精油组合可增强断奶仔猪肠道对 LPS 刺激的抵抗力。

IF 6.3 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Chang Cui, Yulong Wei, Yibo Wang, Wen Ma, Xiaoyu Zheng, Jun Wang, Ziwei Ma, Caichi Wu, Licui Chu, Shihai Zhang, Wutai Guan, Fang Chen
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引用次数: 0

摘要

背景:将苯甲酸和精油(BAO)结合使用可减轻断奶过程中的肠道损伤,其益处已得到充分证实,但详细的内在机制尚未完全阐明。以往的研究主要集中在 BAO 对肠道损伤的修复作用上,而忽视了它在增强肠道抗应激能力方面的潜力:在本研究中,我们采用改进的实验程序研究了 BAO 对 LPS 诱导的应激的预保护作用。仔猪预先补充 BAO 14 d,然后用 LPS 或生理盐水进行挑战,收集血液和肠道样本:结果:我们的研究结果表明,补充 BAO 能显著提高仔猪的最终体重、平均日增重和采食量/增重比。此外,补充 BAO 还对肠道微生物群的组成产生了积极影响,增加了有益的放线菌群和 Alloprevotella,同时减少了有害的脱硫菌群、普雷沃特氏菌和震旦梭菌。此外,补充 BAO 还能有效缓解急性 LPS 挑战引起的氧化紊乱和炎症反应。血浆中 T-AOC、SOD 和 GSH 水平的升高以及 MDA、TNF-α 和 IL-6 水平的降低证明了这一点。此外,与未补充 BAO 的仔猪相比,接受 LPS 挑战并预先补充 BAO 的仔猪的肠道形态结构有了显著改善,肠道完整性得到增强,这体现在 Occludin 和 Claudin-1 的表达水平得到恢复。进一步分析表明,在 LPS 挑战下,补充 BAO 可提高 GSH-Px 水平,降低 MDA 水平,从而增强空肠抗氧化能力,并刺激 Nrf2 信号通路的激活。此外,在饲喂 BAO 的仔猪空肠中还观察到 TLR4/NF-κB/MAPK 信号通路活化和促炎因子的减少:总之,我们的研究表明,预先添加 BAO 可通过改善肠道微生物群组成、强化肠道屏障以及增强抗氧化和抗炎能力来提高断奶仔猪的抗应激能力。这些作用与 Nrf2 和 TLR4/NF-κB/MAPK 信号通路的激活密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dietary supplementation of benzoic acid and essential oils combination enhances intestinal resilience against LPS stimulation in weaned piglets.

Background: The benefits of combining benzoic acid and essential oils (BAO) to mitigate intestinal impairment during the weaning process have been well established, while the detailed underlying mechanism has not been fully elucidated. Previous research has primarily focused on the reparative effects of BAO on intestinal injury, while neglecting its potential in enhancing intestinal stress resistance.

Methods: In this study, we investigated the pre-protective effect of BAO against LPS-induced stress using a modified experimental procedure. Piglets were pre-supplemented with BAO for 14 d, followed by a challenge with LPS or saline to collect blood and intestinal samples.

Results: Our findings demonstrated that BAO supplementation led to significant improvements in piglets' final weight, average daily gain, and feed intake/body gain ratio. Additionally, BAO supplementation positively influenced the composition of intestinal microbiota, increasing beneficial Actinobacteriota and Alloprevotella while reducing harmful Desulfobacterota, Prevotella and Oscillospira. Furthermore, BAO supplementation effectively mitigated oxidative disturbances and inflammatory responses induced by acute LPS challenge. This was evidenced by elevated levels of T-AOC, SOD, and GSH, as well as decreased levels of MDA, TNF-α, and IL-6 in the plasma. Moreover, piglets subjected to LPS challenge and pre-supplemented with BAO exhibited significant improvements in intestinal morphological structure and enhanced integrity, as indicated by restored expression levels of Occludin and Claudin-1 compared to the non-supplemented counterparts. Further analysis revealed that BAO supplementation enhanced the jejunal antioxidative capacity by increasing GSH-Px levels and decreasing MDA levels under the LPS challenge and stimulated the activation of the Nrf2 signaling pathway. Additionally, the reduction of TLR4/NF-κB/MAPK signaling pathways activation and proinflammatory factor were also observed in the jejunal of those piglets fed with BAO.

Conclusions: In summary, our study demonstrates that pre-supplementation of BAO enhances the anti-stress capacity of weaned piglets by improving intestinal microbiota composition, reinforcing the intestinal barrier, and enhancing antioxidative and anti-inflammatory capabilities. These effects are closely associated with the activation of Nrf2 and TLR4/NF-κB/MAPK signaling pathways.

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CiteScore
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