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草药-海洋化合物(HESA-A)对流感病毒感染力的衰减作用:在 MDCK 细胞中的体外研究。

Attenuation of influenza virus infectivity with herbal-marine compound (HESA-A): an in vitro study in MDCK cells.

机构信息

Institute of Bioscience, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia.

出版信息

Virol J. 2012 Feb 16;9:44. doi: 10.1186/1743-422X-9-44.

DOI:10.1186/1743-422X-9-44
PMID:22340010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3296628/
Abstract

BACKGROUND

The influenza virus is still one of the most important respiratory risks affecting humans which require effective treatments. In this case, traditional medications are of interest. HESA-A is an active natural biological compound from herbal-marine origin. Previous studies have reported that the therapeutic properties of HESA-A are able to treat psoriasis vulgaris and cancers. However, no antiviral properties have been reported.

METHODS

This study was designed to investigate the potential antiviral properties of HESA-A and its effects in modulating TNF-α and IL-6 cytokine levels. HESA-A was prepared in normal saline as a stock solution (0.8 mg/ml, pH = 7.4). Percentages of cell survival when exposed to different concentrations of HESA-A at different time intervals was determined by MTT assay. To study the potential antiviral activity of HESA-A, Madin-Darby Canine Kidney (MDCK) cells were treated with the effective concentration (EC50) of HESA-A (0.025 mg/ml) and 100 TCID50/0.1 ml of virus sample under different types of exposure.

RESULTS

Based on the MTT method and hemagglutination assay (HA), HESA-A is capable of improving cell viability to 31% and decreasing HA titre to almost 99% in co-penetration exposures. In addition, based on quantitative real-time PCR (qRT-PCR) and enzyme-linked immunosorbent assay (ELISA), it was found that HESA-A causes decrements in TNF-α and IL-6 cytokine expressions, which was significant for TNF-α (p ≤ 0.05) but not for IL-6.

CONCLUSION

In conclusion, HESA-A was effective against influenza infection through suppressing cytokine expression.

摘要

背景

流感病毒仍然是影响人类的最重要的呼吸道风险之一,需要有效的治疗方法。在这种情况下,传统药物受到关注。HESA-A 是一种源自草药-海洋的活性天然生物化合物。先前的研究报告称,HESA-A 的治疗特性能够治疗寻常型银屑病和癌症。但是,尚未报道其抗病毒特性。

方法

本研究旨在研究 HESA-A 的潜在抗病毒特性及其调节 TNF-α 和 IL-6 细胞因子水平的作用。将 HESA-A 在生理盐水(pH = 7.4)中制备为储备溶液(0.8mg/ml)。通过 MTT 测定法确定在不同浓度的 HESA-A 下暴露于不同时间间隔时细胞的存活率百分比。为了研究 HESA-A 的潜在抗病毒活性,用有效浓度(EC50)的 HESA-A(0.025mg/ml)和 100TCID50/0.1ml 病毒样品处理 Madin-Darby 犬肾(MDCK)细胞在不同类型的暴露下。

结果

根据 MTT 法和血凝(HA)测定法,HESA-A 能够将细胞活力提高到 31%,并将 HA 滴度降低到几乎 99%的共渗透暴露。此外,根据实时定量 PCR(qRT-PCR)和酶联免疫吸附测定(ELISA),发现 HESA-A 导致 TNF-α 和 IL-6 细胞因子表达减少,对 TNF-α 有显著影响(p≤0.05),但对 IL-6 没有影响。

结论

总之,HESA-A 通过抑制细胞因子表达对流感感染有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a91/3296628/9873c0c9f8b6/1743-422X-9-44-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a91/3296628/9e3c13fe672c/1743-422X-9-44-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a91/3296628/9873c0c9f8b6/1743-422X-9-44-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a91/3296628/9e3c13fe672c/1743-422X-9-44-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a91/3296628/9873c0c9f8b6/1743-422X-9-44-2.jpg

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