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首页> 外文期刊>Naunyn-Schmiedeberg's Archives of Pharmacology >Targeting HMGB1/TLR4 axis and miR-21 by rosuvastatin: role in alleviating cholestatic liver injury in a rat model of bile duct ligation
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Targeting HMGB1/TLR4 axis and miR-21 by rosuvastatin: role in alleviating cholestatic liver injury in a rat model of bile duct ligation

机译:罗萨伐他汀靶向HMGB1 / TLR4轴和MIR-21:在缓解胆管结扎大鼠模型中缓解胆管肝损伤的作用

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摘要

Many pathways are involved in the association between biliary obstruction and liver injury. We investigated the intervention influence and effect of rosuvastatin (Rvs) on the high mobility group protein 1 (HMGB1)/toll-like receptor-4 (TLR4) axis and microRNA-21 (miR-21) in cholestatic liver injury. This model was performed by ligating common bile duct of Wistar rats. Saline and Rvs were orally administrated by gastric gavages. Liver and blood samples were collected and subjected to molecular and biochemical evaluation. We found that the daily oral administration of Rvs was protective against the occurrence of cholestatic liver injury. This was evident from the results of hepatic, oxidative stress, and inflammatory biomarkers. This study also revealed the Rvs inhibitory effect on the HMGB1/TLR4 intracellular signaling axis as evidenced by decreasing the levels of nuclear factor (NF), tumor necrosis factor (TNF), and interleukin 6 (IL6) production. Furthermore, Rvs-treated group showed a significant reduction in the expression of miR-21 in comparison to the untreated group. Accordingly, rosuvastatin interference with the HMGB1/TLR4 and miR-21 expression could explain its hepatoprotective effect in cholestatic liver injury.
机译:许多途径涉及胆道阻塞与肝损伤之间的关联。我们研究了胆汁肝损伤中罗斯汀(RVS)对高迁移率组蛋白1(HMGB1)/ Toll样受体-4(TLR4)轴和MicroRNA-21(miR-21)的干预影响和影响。通过连接Wistar大鼠的共同胆管进行该模型。盐水和rvs由胃饲料口服给予。收集肝脏和血液样品并进行分子和生化评估。我们发现每日口服RVS对胆汁淤积肝损伤的发生是保护的。从肝,氧化胁迫和炎症生物标志物的结果中显而易见。本研究还揭示了对HMGB1 / TLR4细胞内信号轴的RVS抑制作用,如通过降低核因子(NF),肿瘤坏死因子(TNF)和白细胞介素6(IL6)生产的水平证明。此外,RVS处理基团与未处理的基团相比,MiR-21的表达显着降低。因此,对HMGB1 / TLR4和miR-21表达的罗萨伐他汀干扰可以解释其在胆汁淤积肝损伤中的肝脏保护作用。

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