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Anti HSV-1 Activity of Halistanol Sulfate and Halistanol Sulfate C Isolated from Brazilian Marine Sponge Petromica citrina (Demospongiae)

机译:从巴西海洋海绵Petromica citrina(Demospongiae)分离得到的硫酸四氢萘酚和硫酸四氢萘酚的抗HSV-1活性

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摘要

The n-butanol fraction (BF) obtained from the crude extract of the marine sponge Petromica citrina, the halistanol-enriched fraction (TSH fraction), and the isolated compounds halistanol sulfate (>1) and halistanol sulfate C (>2), were evaluated for their inhibitory effects on the replication of the Herpes Simplex Virus type 1 (HSV-1, KOS strain) by the viral plaque number reduction assay. The TSH fraction was the most effective against HSV-1 replication (SI = 15.33), whereas compounds >1 (SI = 2.46) and >2 (SI = 1.95) were less active. The most active fraction and these compounds were also assayed to determine the viral multiplication step(s) upon which they act as well as their potential synergistic effects. The anti-HSV-1 activity detected was mediated by the inhibition of virus attachment and by the penetration into Vero cells, the virucidal effect on virus particles, and by the impairment in levels of ICP27 and gD proteins of HSV-1. In summary, these results suggest that the anti-HSV-1 activity of TSH fraction detected is possibly related to the synergic effects of compounds >1 and >2.
机译:从海生海绵Petromica citrina的粗提物中提取的正丁醇馏分(BF),富含卤代斯坦醇的馏分(TSH馏分)以及分离的化合物硫酸卤代乙醇(> 1 )和硫酸卤代醇C (> 2 ),通过减少病毒斑块数评估了其对1型单纯疱疹病毒(HSV-1,KOS株)复制的抑制作用。 TSH组分对HSV-1复制最有效(SI = 15.33),而化合物> 1 (SI = 2.46)和> 2 (SI = 1.95)活性较低。还测定了活性最高的部分和这些化合物,以确定它们所作用的病毒增殖步骤以及它们潜在的协同作用。检测到的抗HSV-1活性是通过抑制病毒附着,渗透到Vero细胞,对病毒颗粒的杀病毒作用以及HSV-1的ICP27和gD蛋白水平的降低来介导的。总之,这些结果表明,检测到的TSH组分的抗HSV-1活性可能与化合物> 1 和> 2 的协同作用有关。

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