This study is to synthesize sulfated Angelica polysaccharides (APSs) and investigate the activity of one of the sulfated derivatives APS-1 on murine leukemia virus in vivo. Six sulfated derivatives with degree of sulfation ranging from 0.68 to 1.91 were obtained. And the virus replication was inhibited by APS-1 at the dose of 10 and 30 mg/kg (26% and 30% inhibition respectively). Furthermore, both the percentage of CD4(+) cells and CD4(+)/CD8(+) ratio in peripheral blood cells were significantly enhanced by APS-1 at 3-30 mg/kg. In addition, the reduced thymus/body weight index by murine leukemia virus infection was increased by ASP-1 in a dose dependent manner. These results suggest that APS-1 could not only inhibit virus replication, but also improve the immune function. APS-1 may be a potential new and better antiviral drug.

译文

本研究旨在合成硫酸化当归多糖 (APSs),并研究其中一种硫酸化衍生物APS-1对小鼠白血病病毒的体内活性。获得了六种硫酸化度为0.68至1.91的硫酸化衍生物。APS-1以10和30 mg/kg的剂量抑制病毒复制 (分别抑制26% 和30%)。此外,以3-30 mg/kg的APS-1可显着提高外周血细胞中CD4 () 细胞的百分比和CD4 ()/CD8 () 比率。此外,ASP-1以剂量依赖性方式增加了鼠白血病病毒降低的胸腺/体重指数。这些结果表明,APS-1不仅可以抑制病毒复制,而且可以提高免疫功能。APS-1可能是一种潜在的新型更好的抗病毒药物。

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