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黄酮类化合物抗肠道病毒 71 型感染的体外和新生小鼠体内的抗病毒功效。

Antiviral Efficacy of Flavonoids against Enterovirus 71 Infection in Vitro and in Newborn Mice.

机构信息

National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University, Changchun 130012, China.

Key Laboratory for Molecular Enzymology and Engineering of the Ministry of Education, School of Life Sciences, Jilin University, Changchun 130012, China.

出版信息

Viruses. 2019 Jul 7;11(7):625. doi: 10.3390/v11070625.

Abstract

Enterovirus 71 (EV71) infection is known to cause hand, foot, and mouth disease (HFMD), which is associated with neurological complications; however, there is currently no effective treatment for this infection. Flavonoids are a large group of naturally occurring compounds with multiple bioactivities, and the inhibitory effects of several flavonoids against EV71 have been studied in cell cultures; however, to date, there are no reported data on their effects in animal models. In this study, we confirmed the in vitro activities of eight flavonoids against EV71 infection, based on the inhibition of cytopathic effects. Moreover, these flavonoids were found to reduce viral genomic RNA replication and protein synthesis. We further demonstrated the protective efficacy of these flavonoids in newborn mice challenged with a lethal dose of EV71. Apigenin, luteolin, kaempferol, formononetin, and penduletin conferred survival protection of 88.89%, 91.67%, 88.89%, 75%, and 66.67%, respectively, from the lethal EV71 challenge. In addition, isorhamnetin provided the highest mice survival protection of 100% at a dose of 10 mg/kg. This study, to the best of our knowledge, is the first to evaluate the in vivo anti-EV7l activities of multiple flavonoids, and we accordingly identified flavonoids as potential leading compounds for anti-EV71 drug development.

摘要

肠道病毒 71 型(EV71)感染已知会引起手足口病(HFMD),并伴有神经并发症;然而,目前针对这种感染还没有有效的治疗方法。类黄酮是一大类具有多种生物活性的天然化合物,已有研究表明几种类黄酮在细胞培养物中对 EV71 具有抑制作用;然而,迄今为止,尚无关于它们在动物模型中作用的报道数据。在这项研究中,我们基于对细胞病变效应的抑制作用,证实了 8 种类黄酮在体外对 EV71 感染的活性。此外,这些类黄酮被发现可减少病毒基因组 RNA 的复制和蛋白合成。我们进一步在新生小鼠模型中证明了这些类黄酮对致死剂量 EV71 攻击的保护作用。白杨素、木樨草素、山奈酚、芒柄花素和 Pendulletin 分别对致死性 EV71 攻击的保护率为 88.89%、91.67%、88.89%、75%和 66.67%。此外,异鼠李素在 10mg/kg 的剂量下提供了最高的 100%的小鼠存活率保护。据我们所知,这项研究首次评估了多种类黄酮在体内抗 EV7l 的活性,因此我们将类黄酮鉴定为抗 EV71 药物开发的潜在先导化合物。

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