首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Expression of antiviral cytokines in Crandell-Reese feline kidney cells pretreated with Korean red ginseng extract or ginsenosides
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Expression of antiviral cytokines in Crandell-Reese feline kidney cells pretreated with Korean red ginseng extract or ginsenosides

机译:红参提取物或人参皂甙预处理后的克兰德尔·里斯猫肾细胞中抗病毒细胞因子的表达

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摘要

The antiviral activity and protective mechanism of Korean red ginseng (KRG) is not well understood. The aim of this study was to investigate the protective mechanism of KRG extract and ginsenosides against feline calicivirus (FCV), a human norovirus surrogate. CRFK cells that were pretreated for 48 h with 10 mu g/mL of KRG extract or purified ginsenoside Rb1 or Rg1, were inoculated with FCV. RNA extracted from each treated group was examined for the expression of antiviral cytokines, including interferon-alpha (IFN-alpha), interferon-beta (IFN-beta), interferon-omega (IFN-omega), Mx, and zinc finger antiviral protein shorter isoform (ZAPS), by relative real-time reverse transcription-polymerase chain reaction. mRNA expression of IFN-alpha, IFN-beta, IFN-alpha, Mx, and ZAPS was significantly induced in the FCV-challenged group pretreated with the KRG extract or ginsenosides, and it was higher than the group treated with FCV alone. Mx protein expression was confirmed by western blotting of CRFK cells pretreated with the ginsenoside Rb1 or with Rg1. Induction of antiviral cytokines contributes to the reduction of the viral titer in CRFK cells pretreated with the KRG extract and purified ginsenosides. In future studies, the antiviral protective mechanism of KRG should be demonstrated using other viruses such as human norovirus. (C) 2014 Elsevier Ltd. All rights reserved.
机译:高丽人参的抗病毒活性和保护机制尚不清楚。这项研究的目的是调查KRG提取物和人参皂苷对猫诺维病毒替代品猫杯状病毒(FCV)的保护机制。用FCV接种用10μg / mL的KRG提取物或纯化的人参皂甙Rb1或Rg1预处理48小时的CRFK细胞。检查从每个治疗组中提取的RNA的抗病毒细胞因子的表达,包括干扰素-α(IFN-alpha),干扰素-β(IFN-beta),干扰素-ω(IFN-omega),Mx和锌指抗病毒蛋白通过相对实时逆转录-聚合酶链反应的短异构体(ZAPS)。在用KRG提取物或人参皂苷预处理的FCV攻击组中,IFN-α,IFN-β,IFN-α,Mx和ZAPS的mRNA表达被显着诱导,并且高于单独使用FCV的组。通过用人参皂苷Rb1或Rg1预处理的CRFK细胞的蛋白质印迹证实了Mx蛋白的表达。抗病毒细胞因子的诱导有助于减少用KRG提取物和纯化的人参皂甙预处理的CRFK细胞中的病毒滴度。在未来的研究中,应该使用其他病毒(例如人类诺如病毒)证明KRG的抗病毒保护机制。 (C)2014 Elsevier Ltd.保留所有权利。

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