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34-Dicaffeoylquinic Acid a Major Constituent of Brazilian Propolis Increases TRAIL Expression and Extends the Lifetimes of Mice Infected with the Influenza A Virus

机译:34-二咖啡酰奎尼酸巴西蜂胶的主要成分可提高TRAIL的表达并延长感染甲型流感病毒的小鼠的寿命

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摘要

Brazilian green propolis water extract (PWE) and its chemical components, caffeoylquinic acids, such as 3,4-dicaffeoylquinic acid (3,4-diCQA), act against the influenza A virus (IAV) without influencing the viral components. Here, we evaluated the anti-IAV activities of these compounds in vivo. PWE or PEE (Brazilian green propolis ethanol extract) at a dose of 200 mg/kg was orally administered to Balb/c mice that had been inoculated with IAV strain A/WSN/33. The lifetimes of the PWE-treated mice were significantly extended compared to the untreated mice. Moreover, oral administration of 3,4-diCQA, a constituent of PWE, at a dose of 50 mg/kg had a stronger effect than PWE itself. We found that the amount of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) mRNA in the mice that were administered 3,4-diCQA was significantly increased compared to the control group, while H1N1 hemagglutinin (HA) mRNA was slightly decreased. These data indicate that PWE, PEE or 3,4-diCQA possesses a novel and unique mechanism of anti-influenza viral activity, that is, enhancing viral clearance by increasing TRAIL.
机译:巴西绿色蜂胶水提取物(PWE)及其化学成分,咖啡酰奎尼酸,例如3,4-二咖啡酰奎尼酸(3,4-diCQA),可在不影响病毒组分的情况下抵抗甲型流感病毒(IAV)。在这里,我们评估了这些化合物在体内的抗IAV活性。将200μmg/ kg的PWE或PEE(巴西绿蜂胶乙醇提取物)口服给已接种IAV株A / WSN / 33的Balb / c小鼠。与未治疗的小鼠相比,PWE治疗的小鼠的寿命显着延长。而且,以50μmg/ kg的剂量口服给予PWE的成分3,4-diCQA具有比PWE本身更强的作用。我们发现,与对照组相比,施用3,4-diCQA的小鼠中肿瘤坏死因子相关的凋亡诱导配体(TRAIL)mRNA的量显着增加,而H1N1血凝素(HA)mRNA则略有降低。这些数据表明,PWE,PEE或3,4-diCQA具有新颖且独特的抗流感病毒活性机制,即通过增加TRAIL来提高病毒清除率。

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