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Proanthocyanidin from Blueberry Leaves Suppresses Expression of Subgenomic Hepatitis C Virus RNA*

机译:蓝莓叶中的原花青素抑制亚基因组丙型肝炎病毒RNA *的表达

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摘要

Hepatitis C virus (HCV) infection is a major cause of chronic liver disease such as chronic hepatitis, cirrhosis, and hepatocellular carcinoma. While searching for new natural anti-HCV agents in agricultural products, we found a potent inhibitor of HCV RNA expression in extracts of blueberry leaves when examined in an HCV subgenomic replicon cell culture system. This activity was observed in a methanol extract fraction of blueberry leaves and was purified by repeated fractionations in reversed-phase high-performance liquid chromatography. The final purified fraction showed a 63-fold increase in specific activity compared with the initial methanol extracts and was composed only of carbon, hydrogen, and oxygen. Liquid chromatography/mass-ion trap-time of flight analysis and butanol-HCl hydrolysis analysis of the purified fraction revealed that the blueberry leaf-derived inhibitor was proanthocyanidin. Furthermore, structural analysis using acid thiolysis indicated that the mean degree of polymerization of the purified proanthocyanidin was 7.7, consisting predominantly of epicatechin. Proanthocyanidin with a polymerization degree of 8 to 9 showed the greatest potency at inhibiting the expression of subgenomic HCV RNA. Purified proanthocyanidin showed dose-dependent inhibition of expression of the neomycin-resistant gene and the NS-3 protein gene in the HCV subgenome in replicon cells. While characterizing the mechanism by which proanthocyanidin inhibited HCV subgenome expression, we found that heterogeneous nuclear ribonucleoprotein A2/B1 showed affinity to blueberry leaf-derived proanthocyanidin and was indispensable for HCV subgenome expression in replicon cells. These data suggest that proanthocyanidin isolated from blueberry leaves may have potential usefulness as an anti-HCV compound by inhibiting viral replication.
机译:丙型肝炎病毒(HCV)感染是慢性肝病(例如慢性肝炎,肝硬化和肝细胞癌)的主要原因。在寻找农产品中的新型天然抗HCV药物时,我们在HCV亚基因组复制子细胞培养系统中检查了蓝莓叶提取物中的HCV RNA表达的有效抑制剂。在蓝莓叶的甲醇提取物级分中观察到该活性,并通过在反相高效液相色谱中重复分级分离将其纯化。与最初的甲醇提取物相比,最终纯化的馏分的比活性提高了63倍,并且仅由碳,氢和氧组成。纯化级分的液相色谱/质谱离子飞行时间分析和丁醇-HCl水解分析表明,蓝莓叶衍生的抑制剂为原花青素。此外,使用酸性硫解的结构分析表明,纯化的原花色素的平均聚合度为7.7,主要由表儿茶素组成。原花青素的聚合度为8至9,显示出抑制亚基因组HCV RNA表达的最大能力。纯化的原花青素显示出复制子细胞中HCV亚基因组中新霉素抗性基因和NS-3蛋白基因表达的剂量依赖性抑制。在表征原花青素抑制HCV亚基因组表达的机制的同时,我们发现异质核糖核蛋白A2 / B1与蓝莓叶原花青素具有亲和力,并且对于复制子细胞中HCV亚基因组的表达是必不可少的。这些数据表明,从蓝莓叶中分离出的原花色素可能通过抑制病毒复制而具有作为抗HCV化合物的潜在用途。

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