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欧白芷提取物对单纯疱疹病毒-1和柯萨奇病毒B3感染的抗病毒作用

Antiviral effect of compounds derived from Angelica archangelica L. on Herpes simplex virus-1 and Coxsackievirus B3 infections.

作者信息

Rajtar Barbara, Skalicka-Woźniak Krystyna, Świątek Łukasz, Stec Agnieszka, Boguszewska Anastazja, Polz-Dacewicz Małgorzata

机构信息

Department of Virology, Medical University of Lublin, Poland.

Department of Pharmacognosy with Medicinal Plant Unit, Medical University of Lublin, Poland.

出版信息

Food Chem Toxicol. 2017 Nov;109(Pt 2):1026-1031. doi: 10.1016/j.fct.2017.05.011. Epub 2017 May 6.

Abstract

The dichloromethane extract from fruits of Angelica archangelica L. was separated by the modern high-performance countercurrent chromatography (HPCCC). The extract and five pure compounds: xanthotoxin, bergapten, imperatorin, phellopterin and isoimperatorin, and the mixture of imperatorin and phellopterin, have been studied as the potential antiviral agents against Herpes simplex virus type l and Coxsackievirus B3. The cytotoxicity was measured using the MTT method. Compounds were tested for the in vitro antiviral activity using the cytopathic effect (CPE) inhibitory assay and by the virus titre reduction assay. Real-time PCR was used to quantify the relative inhibition of the HSV-1 replication. The results indicate that the highest activity was demonstrated by the extract, imperatorin, phellopterin and the mixture of imperatorin and phellopterin, reducing the HSV-1 replication by 5.61 log, 4.7 log, 3.01 log and 3.73 log, respectively. The influence of isolated compounds on the CVB3 replication was not significant. Only the extract caused the decrease in the titre of virus in relation to the virus control. Our results show that coumarins of A. archangelica L. might be a potential candidate for the development of the alternative natural anti- HSV-1 compound. Moreover, the presence of isopentenyloxy moiety at C-8 position significantly improves their activity.

摘要

采用现代高效逆流色谱法(HPCCC)对欧当归果实的二氯甲烷提取物进行分离。该提取物以及五种纯化合物:花椒毒素、佛手柑内酯、欧前胡素、异欧前胡素和紫花前胡素,还有欧前胡素与紫花前胡素的混合物,已被作为抗1型单纯疱疹病毒和柯萨奇病毒B3的潜在抗病毒剂进行研究。采用MTT法测定细胞毒性。使用细胞病变效应(CPE)抑制试验和病毒滴度降低试验对化合物的体外抗病毒活性进行检测。采用实时荧光定量PCR对HSV-1复制的相对抑制作用进行定量分析。结果表明,提取物、欧前胡素、紫花前胡素以及欧前胡素与紫花前胡素的混合物表现出最高活性,分别使HSV-1复制减少5.61对数、4.7对数、3.01对数和3.73对数。分离得到的化合物对CVB3复制的影响不显著。只有提取物使病毒滴度相对于病毒对照有所降低。我们的结果表明,欧当归中的香豆素可能是开发替代天然抗HSV-1化合物的潜在候选物。此外,C-8位异戊烯氧基部分的存在显著提高了它们的活性。

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