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(–)-Epigallocatechin-3-gallate protects mice from concanavalin A-induced hepatitis through suppressing immune-mediated liver injury

机译:(–)-Epigallocatechin-3-gallate通过抑制免疫介导的肝损伤,保护小鼠免受伴刀豆球蛋白A诱发的肝炎

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摘要

(–)-Epigallocatechin-3-gallate (EGCG) is the major active component of green tea. Increasing evidence has suggested that EGCG exhibits anti-inflammatory, anti-oxidant and immunosuppressive effects. In this study, we investigated the effect of EGCG on concanavalin A (ConA)-induced hepatitis (CIH) in mice, a model of immune-mediated liver injury in humans. We pretreated mice with EGCG before ConA injection, and then measured alanine aminotransferase (ALT) levels in plasma, inflammatory infiltration and hepatocyte apoptosis in liver. Potential therapeutic mechanisms were elucidated further by measuring several inflammatory mediators. Mice pretreated with EGCG exhibited much less increased ALT levels in plasma, reduced inflammatory infiltration and hepatocyte apoptosis in liver compared with control mice pretreated with vehicle solutions. We further investigated the mechanisms of the protective effects of EGCG. In EGCG-pretreated mice, we found abrogated tumour necrosis factor (TNF)-α and interferon (IFN)-γ at both protein levels in plasma and mRNA levels in liver. At the same time, the concentration of nitrite in plasma and inducible nitric oxide synthase production in liver were both down-regulated in these mice. Moreover, IFN-inducible protein-10 and macrophage inflammatory protein-1α expressions in liver were decreased significantly. Therefore, EGCG is capable of regulating immune-mediated liver injury in vivo. The protective effect depended on its suppressive effect on the production of important inflammatory mediators.
机译:(-)-表没食子儿茶素-3-没食子酸酯(EGCG)是绿茶的主要活性成分。越来越多的证据表明,EGCG具有抗炎,抗氧化和免疫抑制作用。在这项研究中,我们研究了EGCG对伴刀豆球蛋白A(ConA)诱导的小鼠肝炎(CIH)的影响,小鼠是人免疫介导的肝损伤模型。我们在ConA注射之前用EGCG对小鼠进行了预处理,然后测量了血浆中丙氨酸转氨酶(ALT)的水平,肝脏的炎症浸润和肝细胞凋亡。通过测量几种炎症介质进一步阐明了潜在的治疗机制。与用溶媒溶液预处理的对照小鼠相比,用EGCG预处理的小鼠血浆中的ALT水平升高,肝脏的炎性浸润和肝细胞凋亡降低的幅度要小得多。我们进一步研究了EGCG保护作用的机制。在EGCG预处理的小鼠中,我们发现血浆蛋白水平和肝脏mRNA水平均消除了肿瘤坏死因子(TNF)-α和干扰素(IFN)-γ。同时,这些小鼠血浆中亚硝酸盐的浓度和肝脏中可诱导的一氧化氮合酶的产生均被下调。此外,肝中IFN-诱导蛋白10和巨噬细胞炎性蛋白-1α的表达显着降低。因此,EGCG能够在体内调节免疫介导的肝损伤。保护作用取决于其对重要炎症介质产生的抑制作用。

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