Morrison V, Ashby J
Zeneca Central Toxicology Laboratory, Nr Macclesfield, Cheshire, UK.
Mutagenesis. 1994 Jul;9(4):361-5. doi: 10.1093/mutage/9.4.361.
Five positive and four negative reports of the activity of dimethylnitrosamine (DMN) in the mouse bone marrow micronucleus assay exist in the literature: toxicity and micronucleus experiments have been conducted to resolve this finely balanced conflict of data. The maximum dose at which mice can survive a single treatment with DMN is 10-12.5 mg/kg. A dose of 15 mg/kg is lethal within 4 days while higher doses are lethal within 1-2 days. None the less, micronucleus assays can be conducted with DMN up to dose levels of 100 mg/kg if animals are sampled within 24 h of dosing, i.e. before they die. We have demonstrated clear positive assay responses for DMN at lethal dose levels (30 and 60 mg/kg). At non-lethal (maximum tolerated) dose-levels (10 and 12.5 mg/kg) marginal positive or negative responses were observed. Both the oral and intraperitoneal injection routes of exposure have been studied. These observations enable the nine previous and divergent literature reports to be explained. The present data for DMN focus attention on the need to consider carefully the selection of dose-levels for use in short-term in vivo genotoxicity assays. In particular, it is suggested that many of the conflicts of assay data that exist in the literature may be caused by the failure of investigators to study, adequately, the toxicity of chemicals. It is proposed that positive genotoxicity test data generated only at lethal dose-levels are of no toxicological value.
文献中存在关于二甲基亚硝胺(DMN)在小鼠骨髓微核试验中活性的五份阳性报告和四份阴性报告:已进行毒性和微核试验以解决这一数据上的微妙冲突。小鼠单次接受DMN处理能够存活的最大剂量为10 - 12.5毫克/千克。15毫克/千克的剂量在4天内致死,而更高剂量在1 - 2天内致死。尽管如此,如果在给药后24小时内(即动物死亡前)对动物进行采样,DMN可进行高达100毫克/千克剂量水平的微核试验。我们已证明DMN在致死剂量水平(30和60毫克/千克)下有明确的阳性试验反应。在非致死(最大耐受)剂量水平(10和12.5毫克/千克)下观察到边缘性阳性或阴性反应。已研究了口服和腹腔注射两种暴露途径。这些观察结果能够解释之前九份不同的文献报告。DMN的当前数据使人们关注在短期体内遗传毒性试验中仔细选择剂量水平的必要性。特别是,有人提出文献中存在的许多试验数据冲突可能是由于研究人员未能充分研究化学物质的毒性所致。有人提议仅在致死剂量水平产生的阳性遗传毒性试验数据没有毒理学价值。