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Ethanol extract of Polygonum cuspidatum inhibits hepatitis B virus in a stable HBV-producing cell line.

机译:虎杖乙醇提取物可在稳定的HBV产生细胞系中抑制乙型肝炎病毒。

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Chronic hepatitis B virus (HBV) infection is endemic in Asia and its consequences are among the major public health problems in the world. Unfortunately, the therapeutic efficacies of present strategies are still unsatisfactory with a major concern about viral mutation. In search of effective antiviral agent, we examined the efficacy of extracts of Polygonum cuspidatum Sieb. et Zucc. (P. cuspidatum) against HBV in HepG2 2.2.15 cells by quantitative real time polymerase chain reaction. The expressions of viral antigens, HBeAg and HBsAg, were also determined by enzyme linked immunosorbent assay. The ethanol extract of P. cuspidatum could inhibit dose-dependently the production of HBV (p<0.0001) with an effective minimal dosage of 10 microg/ml. The water extract of P. cuspidatum might also inhibit the production of HBV at a higher dosage. The expression of HBsAg was significantly increased by both ethanol extract and water extract of P. cuspidatum dose-dependently (p<0.0001) and time-dependently (p<0.0001). Higher dose of water extract of P. cuspidatum (30 microg/ml) could inhibit the expression of HBeAg (p<0.05). The extract of P. cuspidatum might contain compounds that would contribute to the control of HBV infection in the future. However, its promoting effect on the expression of HBsAg and its cytotoxicity should be monitored. Further purification of the active compounds, identification and modification of their structures to improve the efficacy and decrease the cytotoxicity are required.
机译:慢性乙型肝炎病毒(HBV)感染在亚洲很流行,其后果是世界上主要的公共卫生问题之一。不幸的是,当前策略的治疗效果仍不能令人满意,主要涉及病毒突变。为了寻找有效的抗病毒剂,我们检查了虎杖提取物的功效。 et Zucc。定量实时聚合酶链反应检测HepG2 2.2.15细胞中的猪(P. cuspidatum)抗HBV。还通过酶联免疫吸附测定法测定了病毒抗原HBeAg和HBsAg的表达。虎杖的乙醇提取物可以有效地最小剂量10μg/ ml剂量依赖性地抑制HBV的产生(p <0.0001)。虎杖的水提取物也可能以较高剂量抑制HBV的产生。虎杖乙醇提取物和水提取物均以剂量依赖性(p <0.0001)和时间依赖性(p <0.0001)显着增加HBsAg的表达。较高剂量的虎杖水提取物(30微克/毫升)可以抑制HBeAg的表达(p <0.05)。虎杖的提取物可能含有将来可能有助于控制HBV感染的化合物。但是,应监测其对HBsAg表达的促进作用及其细胞毒性。需要进一步纯化活性化合物,鉴定和修饰其结构以改善功效并降低细胞毒性。

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