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木犀草素对伪狂犬病病毒的体内外抗病毒活性

Antiviral Activity of Luteolin against Pseudorabies Virus In Vitro and In Vivo.

作者信息

Men Xiaoyu, Li Su, Cai Xiaojing, Fu Lian, Shao Yi, Zhu Yan

机构信息

College of Veterinary Medicine, Northeast Agricultural University, Harbin 150038,China.

State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150008, China.

出版信息

Animals (Basel). 2023 Feb 20;13(4):761. doi: 10.3390/ani13040761.

Abstract

Pseudorabies virus (PRV) can cause acute swine disease leading to economic losses worldwide and is a potential causative agent of viral encephalitis in humans. Although effective vaccines are available, an increasing number of variants have emerged in China, and identifying effective antiviral agents against PRV to prevent latent infection is essential. In this study, we assessed the antiviral activity of luteolin against PRV in vitro and in vivo. Luteolin was found to significantly inhibit PRV at a noncytotoxic concentration (70 μM), with an IC of 26.24 μM and a selectivity index of 5.64. Luteolin inhibited the virus at the replication stage and decreased the expression of viral mRNA and gB protein. Luteolin reduced the apoptosis of PRV-infected cells, improved the survival rate of mice after lethal challenge, reduced the viral loads in the liver, kidney, heart, lung, and brain, reduced brain lesions, and slowed inflammation and oxidation reactions. Our results showed that luteolin has promise as a new alternative antiviral drug for PRV infection.

摘要

伪狂犬病病毒(PRV)可引发急性猪病,在全球范围内导致经济损失,并且是人类病毒性脑炎的潜在病原体。尽管有有效的疫苗,但中国出现了越来越多的变异株,因此鉴定针对PRV的有效抗病毒药物以预防潜伏感染至关重要。在本研究中,我们评估了木犀草素在体外和体内对PRV的抗病毒活性。发现木犀草素在非细胞毒性浓度(70μM)下能显著抑制PRV,其半数抑制浓度(IC)为26.24μM,选择性指数为5.64。木犀草素在病毒复制阶段抑制病毒,并降低病毒mRNA和gB蛋白的表达。木犀草素减少了PRV感染细胞的凋亡,提高了致死性攻击后小鼠的存活率,降低了肝脏、肾脏、心脏、肺和脑中的病毒载量,减少了脑部病变,并减缓了炎症和氧化反应。我们的结果表明,木犀草素有望成为一种用于PRV感染的新型替代抗病毒药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e49/9952634/3cc282d653de/animals-13-00761-g001.jpg

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