Coronnello M, Caderni G, Dolara P
Methods Find Exp Clin Pharmacol. 1985 Jan;7(1):29-34.
Various techniques are available for the evaluation of the genotoxic potential of drugs and chemicals, some of which utilize as targets mammalian cells grown in vitro. Among these techniques alkaline elution of DNA has the advantage of rapidity and low cost, and can be performed on easily grown leukemia cell lines. To test the applicability of the method to pharmaceutical compounds, we used DNA-alkaline elution with a series of antiviral agents with variable DNA-damaging activity. 5-Iodo-2'-deoxyuridine (5-IdU), 5-bromo-2'-deoxyuridine (5-BrdU) and 5-trifluoromethyl-2'-deoxyuridine (F3dT) increased the DNA elution rate over controls in a dose-dependent fashion, 9-beta-D-arabinofuranosyladenine (ARA-A) had a marginal effect. 9-(2-Hydroxyethoxymethyl)guanine(acyclovir,ACV) and 5-(2-bromovinyl)-2-deoxyuridine (5-BrVdU), selective antiviral compounds, did not vary alkaline elution profiles. These results fully support the use of alkaline elution of DNA as a standard procedure in the evaluation of the genotoxic effect of drugs.
有多种技术可用于评估药物和化学物质的遗传毒性潜力,其中一些技术将体外培养的哺乳动物细胞作为靶标。在这些技术中,DNA碱性洗脱具有快速和低成本的优点,并且可以在易于培养的白血病细胞系上进行。为了测试该方法对药物化合物的适用性,我们对一系列具有不同DNA损伤活性的抗病毒药物使用了DNA碱性洗脱法。5-碘-2'-脱氧尿苷(5-IdU)、5-溴-2'-脱氧尿苷(5-BrdU)和5-三氟甲基-2'-脱氧尿苷(F3dT)以剂量依赖性方式提高了DNA洗脱率,与对照组相比,9-β-D-阿拉伯呋喃糖基腺嘌呤(ARA-A)有轻微影响。9-(2-羟乙氧基甲基)鸟嘌呤(阿昔洛韦,ACV)和5-(2-溴乙烯基)-2'-脱氧尿苷(5-BrVdU)这两种选择性抗病毒化合物,并未改变碱性洗脱图谱。这些结果充分支持将DNA碱性洗脱作为评估药物遗传毒性作用的标准程序。