首页> 外文期刊>Journal of Agricultural and Food Chemistry >Protective Effect of Ellagic Acid on Concanavalin A-lnduced Hepatitis via Toll-Like Receptor and Mitogen-Activated Protein Kinase/Nuclear Factor kB Signaling Pathways
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Protective Effect of Ellagic Acid on Concanavalin A-lnduced Hepatitis via Toll-Like Receptor and Mitogen-Activated Protein Kinase/Nuclear Factor kB Signaling Pathways

机译:鞣花酸通过Toll样受体和丝裂原活化蛋白激酶/核因子kB信号通路对刀豆素A诱导的肝炎的保护作用

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摘要

Ellagic acid (EA) is present in certain fruits and nuts, including raspberries, pomegranates, and walnuts, and has anti-inflammatory and antioxidant properties. The aims of this study were to examine the protective effect of EA on concanavalin A (Con A)-induced hepatitis and to elucidate its underlying molecular mechanisms in mice. Mice were orally administered EA at different doses before the intravenous delivery of Con A; the different experimental groups were as follows: (i) vehicle control, (ii) Con A alone without EA, (iii) EA at 50 mg/kg, (iv) EA at 100 mg/kg, and (v) EA at 200 mg/kg. We found that EA pretreatment significantly reduced the levels of plasma aminotransferase and liver necrosis in Con A-induced hepatitis. Also, EA significantly decreased the expression levels of the toll-like receptor 2 (TLR2) and TLR4 mRNA and protein in liver tissues. Further, EA decreased the phosphorylation of JNK, ERK1/2, and p38. EA-treated groups showed suppressions of nuclear factor kB (NF-kB) and IkB-a degradation levels in liver tissues. In addition, EA pretreatment decreased the expression of proinflammatory cytokines, such as tumor necrosis factor α (TNF-α), interleukin 6 (IL-6), and interleukin 1β (IL-1β). These results suggest that EA protects against T-cell-mediated hepatitis through TLR and mitogen-activated protein kinase (MAPIC)/NF-kB signaling pathways.
机译:鞣花酸(EA)存在于某些水果和坚果中,包括覆盆子,石榴和核桃,具有抗炎和抗氧化特性。这项研究的目的是检查EA对伴刀豆球蛋白A(Con A)诱导的肝炎的保护作用,并阐明其在小鼠中的潜在分子机制。在静脉内递送Con A之前,以不同剂量口服给小鼠EA。不同的实验组如下:(i)媒介物对照,(ii)没有EA的单独的Con A,(iii)EA在50 mg / kg,(iv)EA在100 mg / kg,和(v)EA在200毫克/千克我们发现,EA预处理可显着降低Con A诱发的肝炎患者血浆氨基转移酶和肝坏死的水平。此外,EA明显降低了肝脏组织中Toll样受体2(TLR2)和TLR4 mRNA和蛋白的表达水平。此外,EA降低了JNK,ERK1 / 2和p38的磷酸化。 EA治疗组在肝组织中显示出对核因子kB(NF-kB)和IkB-a降解水平的抑制作用。此外,EA预处理可降低促炎细胞因子的表达,例如肿瘤坏死因子α(TNF-α),白介素6(IL-6)和白介素1β(IL-1β)。这些结果表明,EA通过TLR和有丝分裂原激活的蛋白激酶(MAPIC)/ NF-kB信号通路保护T细胞介导的肝炎。

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