首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Dehydroepiandrosterone, epiandrosterone and synthetic derivatives inhibit Junin virus replication in vitro.
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Dehydroepiandrosterone, epiandrosterone and synthetic derivatives inhibit Junin virus replication in vitro.

机译:脱氢表雄酮,表雄酮和合成衍生物在体外抑制胡宁病毒复制。

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摘要

In the present paper the in vitro antiviral activity of dehydroepiandrosterone (DHEA), epiandrosterone (EA) and 16 synthetic derivatives against Junin virus (JUNV) replication in Vero cells was studied. DHEA and EA caused a selective inhibition of the replication of JUNV and other members of the Arenaviridae family such as Pichinde virus and Tacaribe virus. The compounds were not virucidal to cell-free JUNV. The impairment of viral replication was not due to an inhibitory effect of the steroids on virus adsorption or internalization. An inhibitory effect of the compounds on JUNV protein synthesis and both intracellular and extracellular virus production was demonstrated. A partial inhibitory action on cell surface expression of JUNV glycoprotein G1 was also detected on DHEA- and EA-treated cultures. Like DHEA and EA, three compounds obtained from EA by chemical synthesis showed selectivity indexes higher than ribavirin, the only antiviral compound that has shown partial efficacy against arenavirus infections.
机译:本文研究了脱氢表雄酮(DHEA),表雄甾酮(EA)和16种合成衍生物对Jeroin病毒(JUNV)在Vero细胞中复制的体外抗病毒活性。 DHEA和EA选择性抑制了JUNV和Arenaviridae家族其他成员(如Pichinde病毒和Tacaribe病毒)的复制。该化合物对无细胞的JUNV无杀伤力。病毒复制的损伤不是由于类固醇对病毒吸附或内在化的抑制作用。证明了这些化合物对JUNV蛋白合成以及细胞内和细胞外病毒产生的抑制作用。在DHEA和EA处理的培养物中也检测到对JUNV糖蛋白G1细胞表面表达的部分抑制作用。像DHEA和EA一样,通过化学合成从EA中获得的三种化合物显示出的选择性指数高于病毒唑,后者是唯一显示出部分抗沙粒病毒感染功效的抗病毒化合物。

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