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人参皂苷 Rb1 是一种免疫刺激剂,具有抗肠道病毒 71 的抗病毒活性。

Ginsenoside Rb1 is an immune-stimulatory agent with antiviral activity against enterovirus 71.

机构信息

College of Pharmaceutical Science, Soochow University, Suzhou, 215123, China.

College of Pharmacy, Guangxi University of Chinese Medicine, Nanning, 530000, China.

出版信息

J Ethnopharmacol. 2021 Feb 10;266:113401. doi: 10.1016/j.jep.2020.113401. Epub 2020 Sep 25.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

According to the theory of traditional Chinese medicine, the main pathogenesis of severe hand, foot and mouth disease (HFMD) is that the heat and wet poisons are deeply trapped in the viscera, which causes the deficiency of Qi and Yin in the patient's body. Ginsenoside Rb1 (Rb1) is the most abundant triterpenoid saponin in Panax quinquefolius L., which has the function of Qi-invigorating and Yin-nourishing. Enterovirus 71 (EV71) is one of the causative pathogens of HFMD, especially the form associated with some lethal complications. Therefore, the therapeutic effect of Rb1 on this disease caused by EV71 infection is worth exploring.

AIM OF THE STUDY

We explored the effective antiviral activities of Rb1 against EV71 in vitro and in vivo and investigated its preliminary antiviral mechanisms.

MATERIAL AND METHODS

EV71-infected two-day-old suckling mice model was employed to detect the antiviral effects of Rb1 in vivo. To detect the antiviral effects of Rb1 in vitro, cytopathic effect (CPE) reduction assay was performed in EV71-infected Rhabdomyosarcoma (RD) cells. Interferon (IFN)-β interference experiment was employed to detect the antiviral mechanism of Rb1.

RESULTS

In this paper, we first found that Rb1 exhibited strong antiviral activities in EV71-infected suckling mice when compared to those of ribavirin. Administration of Rb1 reduced the CPE of EV71-infected RD cells in a dose-dependent manner. Moreover, EV71-induced viral protein-1 (VP-1) expression was significantly reduced by Rb1 administration in vitro and in vivo. Furthermore, Rb1 treatment could induce high cellular and humoral immune responses in vivo. Meanwhile, Rb1 contributed to the enhanced Type I IFN responses and IFN-β knockdown reversed the antiviral activity of Rb1 in vitro.

CONCLUSION

In summary, our findings suggest that Rb1 is an immune-stimulatory agent and provide an insight into therapeutic potentials of Rb1 for the treatment of EV71 infection.

摘要

民族药理学相关性

根据中医理论,重症手足口病(HFMD)的主要发病机制是热毒湿邪深入脏腑,导致患者体内气阴两虚。人参皂苷 Rb1(Rb1)是西洋参中含量最丰富的三萜皂苷,具有益气养阴的作用。肠道病毒 71 型(EV71)是手足口病的病原体之一,特别是与一些致命并发症相关的形式。因此,Rb1 对这种由 EV71 感染引起的疾病的治疗效果值得探索。

研究目的

我们研究了 Rb1 对体内外 EV71 的有效抗病毒活性,并探讨了其初步的抗病毒机制。

材料与方法

采用 EV71 感染的 2 日龄乳鼠模型检测 Rb1 体内的抗病毒作用。在 EV71 感染的横纹肌肉瘤(RD)细胞中进行细胞病变效应(CPE)减少测定,以检测 Rb1 的体外抗病毒作用。采用干扰素(IFN)-β干扰实验检测 Rb1 的抗病毒机制。

结果

本文首次发现,与利巴韦林相比,Rb1 在 EV71 感染的乳鼠中表现出较强的抗病毒活性。Rb1 给药可降低 EV71 感染 RD 细胞的 CPE,呈剂量依赖性。此外,Rb1 给药可显著降低 EV71 诱导的病毒蛋白 1(VP-1)在体内外的表达。此外,Rb1 治疗可在体内诱导高细胞和体液免疫反应。同时,Rb1 增强了Ⅰ型 IFN 反应,IFN-β 敲低逆转了 Rb1 在体外的抗病毒活性。

结论

综上所述,我们的研究结果表明,Rb1 是一种免疫刺激剂,为 Rb1 治疗 EV71 感染提供了治疗潜力。

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