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阿魏酸可预防四氯化碳致小鼠肝损伤。

Ferulic acid protects against carbon tetrachloride-induced liver injury in mice.

机构信息

School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea.

出版信息

Toxicology. 2011 Apr 11;282(3):104-11. doi: 10.1016/j.tox.2011.01.017. Epub 2011 Feb 1.

Abstract

Ferulic acid (FA), isolated from the root of Scrophularia buergeriana, is a phenolic compound possessing antioxidant, anticancer, and antiinflammatory activities. Here, we have investigated the hepatoprotective effect of FA against carbon tetrachloride (CCl(4))-induced acute liver injury. Mice were treated intraperitoneally with vehicle or FA (20, 40, and 80mg/kg) 1h before and 2h after CCl(4) (20μl/kg) injection. The serum activities of aminotransferases and the hepatic level of malondialdehyde were significantly higher after CCl(4) treatment, while the concentration of reduced glutathione was lower. These changes were attenuated by FA. The serum level and mRNA expression of tumor necrosis factor-α significantly increased after CCl(4) treatment, and FA attenuated these increases. The levels of inducible nitric oxide synthase and cyclooxygenase-2 protein and mRNA expression after CCl(4) treatment were significantly higher and FA reduced these increases. CCl(4)-treated mice showed increased nuclear translocation of nuclear factor-κB (NF-κB), and decreased levels of inhibitors of NF-κB in cytosol. Also, CCl(4) significantly increased the level of phosphorylated JNK and p38 mitogen-activated protein (MAP) kinase, and nuclear translocation of activated c-Jun. FA significantly attenuated these changes. We also found that acute CCl(4) challenge induced TLR4, TLR2, and TLR9 protein and mRNA expression, and FA significantly inhibited TLR4 expression. These results suggest that FA protects from CCl(4)-induced acute liver injury through reduction of oxidative damage and inflammatory signaling pathways.

摘要

阿魏酸(FA)从玄参科植物地黄中分离得到,是一种具有抗氧化、抗癌和抗炎活性的酚类化合物。在这里,我们研究了 FA 对四氯化碳(CCl4)诱导的急性肝损伤的保护作用。小鼠腹腔注射 FA(20、40 和 80mg/kg),1h 前和 CCl4(20μl/kg)注射后 2h 各处理 1 次。CCl4 处理后血清转氨酶活性和肝丙二醛水平显著升高,而还原型谷胱甘肽浓度降低,FA 可减弱这些变化。CCl4 处理后血清肿瘤坏死因子-α水平和 mRNA 表达显著增加,FA 可减弱这些增加。CCl4 处理后诱导型一氧化氮合酶和环氧化酶-2 蛋白和 mRNA 表达水平显著升高,FA 可降低这些增加。CCl4 处理的小鼠核因子-κB(NF-κB)核易位增加,细胞浆中 NF-κB 抑制剂水平降低。此外,CCl4 还显著增加了磷酸化 JNK 和 p38 丝裂原活化蛋白(MAP)激酶以及激活的 c-Jun 的核易位。FA 可显著减弱这些变化。我们还发现,急性 CCl4 挑战诱导 TLR4、TLR2 和 TLR9 蛋白和 mRNA 表达,FA 可显著抑制 TLR4 表达。这些结果表明,FA 通过减少氧化损伤和炎症信号通路来保护 CCl4 诱导的急性肝损伤。

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