College of Bioscience and Biotechnology, Hunan Agricultural University, Hunan Provincial Engineering Research Center of Applied Microbial Resources Development for Livestock and Poultry, Changsha, China.
Front Immunol. 2021 Apr 1;12:640305. doi: 10.3389/fimmu.2021.640305. eCollection 2021.
Epigallocatechin gallate (EGCG) has potent biological activity as well as strong antioxidant and anti-inflammatory effects. This study aims to explore the protective effect of EGCG on LPS-induced acute injury. We randomly divided 18 mice into three groups: CON, LPS, and EGCG-LPS. We gave the EGCG-LPS group gavage treatment with EGCG on day 8-15 and an intraperitoneal injection of LPS on day 16 to induce acute injury. The results showed that, compared with the LPS group, the bodyweight of the mice in the EGCG-LPS group increased significantly and effectively inhibited the morphological damage of the jejunum and liver. We measured liver tissue and found that the EGCG gavage treatment significantly inhibited the pro-inflammatory factors () and oxidation indicators (MPO, NO, ALT, and AST) levels increase. The microbiological results showed that the EGCG gavage treatment reshaped the disturbance done to the intestinal microbial community in the mice by LPS, reversed the changes in the abundance ratio of /, and significantly reduced the abundance of . Finally, the serum metabolomics results showed that, when compared with the LPS group, the gavage treatment of EGCG significantly increased the concentration of sphingomyelin (d17:1/17:0), sphingomyelin (d16:1/20:0), and significantly reduced the content of trans-Hexadec-2-enoyl carnitine, and so on. Therefore, we believe that EGCG can protect mice from acute stress induced by LPS while stabilizing gut microbes in general, improving the metabolism of sphingolipids, and inhibiting the content of harmful metabolites.
没食子酸表没食子儿茶素酯(EGCG)具有很强的生物活性,具有很强的抗氧化和抗炎作用。本研究旨在探讨 EGCG 对 LPS 诱导的急性损伤的保护作用。我们将 18 只小鼠随机分为三组:CON、LPS 和 EGCG-LPS。EGCG-LPS 组在第 8-15 天给予 EGCG 灌胃处理,第 16 天给予 LPS 腹腔注射,诱导急性损伤。结果表明,与 LPS 组相比,EGCG-LPS 组小鼠体重显著增加,有效抑制空肠和肝脏的形态损伤。我们测量肝组织发现,EGCG 灌胃处理显著抑制促炎因子()和氧化指标(MPO、NO、ALT 和 AST)水平升高。微生物学结果表明,EGCG 灌胃处理重塑了 LPS 对小鼠肠道微生物群落的干扰,逆转了/丰度比的变化,显著降低了丰度。最后,血清代谢组学结果表明,与 LPS 组相比,EGCG 灌胃处理显著增加了神经鞘磷脂(d17:1/17:0)、神经鞘磷脂(d16:1/20:0)的浓度,显著降低了反式-十六碳-2-烯酰肉碱等的含量。因此,我们认为 EGCG 可以保护小鼠免受 LPS 引起的急性应激,同时稳定肠道微生物群,改善鞘脂代谢,抑制有害代谢物的含量。