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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Hepatorenal protective effects of medicinal herbs in An-Gong-Niu-Huang Wan (AGNH) against cinnabar- and realgar-induced oxidative stress and inflammatory damage in mice
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Hepatorenal protective effects of medicinal herbs in An-Gong-Niu-Huang Wan (AGNH) against cinnabar- and realgar-induced oxidative stress and inflammatory damage in mice

机译:肝脏药草在肺牛黄万(AGNH)对抗豆油和胎儿诱导的氧化胁迫和小鼠炎症损伤的肝脏保护作用

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摘要

An-Gong-Niu-Huang Wan (AGNH) is a famous traditional Chinese medicine prescription that contains cinnabar (HgS) and realgar (As2S2); the clinical practice of AGNH is hindered because both mercury and arsenic are hepatorenal toxic metalloids. It is noted that the cinnabar and realgar in AGNH are not used alone, but rather combined with different kinds of medicinal herbs as a formula to use. In this study, we evaluated the hepatorenal protective effects of the medicinal herbs in AGNH after co-exposure to cinnabar and realgar for 4 weeks in mice. The combination of the herbs in AGNH alleviated cinnabar and realgar-induced histopathological alterations and oxidative stress in the liver and kidneys. Furthermore, in cinnabar and realgar-treated mice, the increased expression levels of inducible enzymes (COX-2 and iNOS) and proinflammatory mediators (IL-1β, TNF-α, PGE2 and NO) in the liver and kidneys were consistently down-regulated when medicinal herbs were combined as a formula. We also found that the herbs could reduce the inflammatory response by the inactivation of the MAPK and PI3K/Akt signaling pathway and the resulting blockade of NF-κB activation. Overall, our data indicates that the herbal medicines in AGNH attenuate cinnabar and realgar-induced hepatorenal toxicity by improving antioxidant competence and suppressing inflammatory injury.
机译:An-Gong-Niu-Huang Wan(Agnh)是一家着名的中医处方,含有Cinnabar(HGS)和雄黄(AS2S2); Agnh的临床实践受到阻碍,因为汞和砷都是肝肾有毒的金属体。值得注意的是,Agnh中的朱砂和雄黄不是单独使用,而是与不同种类的药草相反,作为使用的公式。在这项研究中,我们评估了在小鼠共同暴露于Cinnabar和雄黄后Agnh在ingnh中的肝肾保护作用。在肝脏和肾脏的Agnh缓解的朱奈和胎儿诱导的组织病理学改变和氧化应激中的组合。此外,在朱砂和真人处理的小鼠中,肝脏和肾脏中诱导酶(COX-2和InOS)和促炎介质(IL-1β,TNF-α,PGE2和NO)的表达水平增加始终下调当药物用作配方组合时。我们还发现,草药可以通过MAPK和PI3K / AKT信号通路的失活和所得NF-κB活化阻断的炎症反应。总体而言,我们的数据表明,Agnh中的草药通过改善抗氧化能力和抑制炎症损伤来衰减Cinnabar和胎儿诱发的肝肾毒性。

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