Widell A, Hansson B G, Oberg B, Nordenfelt E
Antiviral Res. 1986 Mar;6(2):103-12. doi: 10.1016/0166-3542(86)90030-6.
A multiwell tissue culture system was developed to study the influence of various substances on hepatitis A virus (HAV) propagation. A panel of 20 substances of different structure types, each with known effect against at least some viruses, was studied at a concentration of 100 microM. Three substances showed reproducible inhibition. The strongest inhibitor, arabinosylcytosine, also produced cytotoxic changes in cells down to a concentration of 1 microM, and its effect was considered as nonspecific. Amantadine and ribavirin showed a moderate effect at 100 microM. A stronger inhibition was seen at 250 and 500 microM, doses that are toxic and impractical for clinical use. Although no promising candidates for antiviral treatment of hepatitis A have emerged from the present study, the assay model described here would seem useful in the screening of substances with inhibitory effects on HAV.
开发了一种多孔组织培养系统,以研究各种物质对甲型肝炎病毒(HAV)增殖的影响。研究了一组20种不同结构类型的物质,每种物质对至少某些病毒都有已知作用,浓度为100微摩尔。三种物质显示出可重复的抑制作用。最强的抑制剂阿糖胞苷,在浓度低至1微摩尔时也会在细胞中产生细胞毒性变化,其作用被认为是非特异性的。金刚烷胺和利巴韦林在100微摩尔时显示出中等效果。在250和500微摩尔时观察到更强的抑制作用,这两个剂量有毒且不适合临床使用。尽管本研究未发现有希望的甲型肝炎抗病毒治疗候选药物,但此处描述的检测模型似乎有助于筛选对HAV有抑制作用的物质。