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首页> 外文期刊>Experimental Biology and Medicine: Journal of the Society for Experimental Biology and Medicine >The inhibitory effect of iridoid glycoside extracted from Fructus Gardeniae on intracellular acidification and extracellular Ca2+ influx induced by influenza A virus
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The inhibitory effect of iridoid glycoside extracted from Fructus Gardeniae on intracellular acidification and extracellular Ca2+ influx induced by influenza A virus

机译:Garden子提取物鸢尾苷对甲型流感病毒引起的细胞内酸化和细胞外Ca2 +流入的抑制作用。

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摘要

Influenza is a serious public health problem that causes severe illnesses and deaths for higher risk populations. Iridoid glycoside is one of the main active components from Fructus Gardeniae with antivirus and anti-inflammatory characteristics. The present study was designed to investigate the inhibitory effect of iridoid glycoside extracted from Fructus Gardeniae (IGE) on influenza and explore the potential mechanism of the action. In vitro, IGE exhibited highest activity against influenza virus A/FM1/47 induced visible cytopathic effect (CPE), with half maximal inhibitory concentration and therapeutic index values of 3.15 mg/mL and 11.37, respectively, and the replication of influenza virus A/FM1/47 was inhibited markedly by IGE at the concentrations of 25, 12.5 and 6.25 mg/mL. In vivo, treatment of mice with IGE decreased pulmonary index, viral titers and M2 protein expression in a dose-dependent manner. IGE increased the declining pHi induced by influenza virus significantly at the concentrations of 25 and 12.5 mg/mL 0.5 or 1 h post-infection, respectively. IGE treatment inhibited elevation of [Ca2+]i significantly at the concentrations of 25 and 12.5 mg/mL 0.5, 1 or 24 h post-infection, respectively. In addition, IGE reduced the rate of early-apoptotic cells at the concentrations of 25, 12.5 and 6.25 mg/mL, but showed no apparent effect on the rate of late-apoptotic cells. Our study demonstrates that IGE possesses antiviral activity against influenza A virus, and the antiviral action might be related to the inhibition of intracellular acidification and Ca2+ influx during fusion and uncoating of influenza replication cycle.
机译:流感是一个严重的公共卫生问题,高危人群会导致严重的疾病和死亡。鸢尾苷是is子中具有抗病毒和抗炎特性的主要活性成分之一。本研究旨在研究从Garden子中提取的艾立得胶苷对流感的抑制作用,并探讨其潜在的作用机理。在体外,IGE表现出对流感病毒A / FM1 / 47诱导的可见细胞病变效应(CPE)的最高活性,最大抑制浓度和治疗指数分别为3.15 mg / mL和11.37的一半,并且流感病毒A /在浓度为25、12.5和6.25 mg / mL的IGE中,FM1 / 47被显着抑制。在体内,用IGE治疗的小鼠以剂量依赖性方式降低了肺指数,病毒滴度和M2蛋白表达。 IGE在感染后0.5或1 h分别以25和12.5 mg / mL的浓度显着增加流感病毒诱导的pHi下降。 IGE处理分别在感染后0.5、1或24 h分别以25和12.5 mg / mL的浓度显着抑制[Ca2 +] i的升高。此外,在25、12.5和6.25 mg / mL的浓度下,IGE降低了早期凋亡细胞的速率,但对晚期凋亡细胞的速率没有明显影响。我们的研究表明,IGE具有抗甲型流感病毒的抗病毒活性,其抗病毒作用可能与抑制流感病毒复制周期融合和脱壳过程中的细胞内酸化和Ca2 +内流有关。

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