Doyle C E, Mackay J M, Ashby J
Zeneca Central Toxicology Laboratory, Macclesfield, Cheshire, UK.
Mutagenesis. 1993 Nov;8(6):583-4. doi: 10.1093/mutage/8.6.583.
De Flora et al. (1991a) have demonstrated a marked protective effect afforded by N-acetylcysteine (NAC) to the liver and lung of rats exposed to benzo[a]pyrene (BP) by intratracheal injection. Due to the protocol used by De Flora et al., BP was inactive in the bone marrow micronucleus assay and, consequently, the possible protective effect of NAC in this tissue could not be assessed. In the present study, three daily administrations of 7,12-dimethylbenzanthracene (DMBA; 15 or 25 mg/kg/day via oral gavage) resulted in the expected increased in micronucleated polychromatic erythrocytes (MPE) in the bone marrow of male C57BL/6 mice 24 h after the final dose. Pretreatment of similar groups of mice with NAC (1 g/kg/day via oral gavage) 5 h before each administration of DMBA had no effect on MPE frequencies. It is concluded that NAC does not have a protective effect on the mouse bone marrow.
德弗洛拉等人(1991年a)已证明,通过气管内注射接触苯并[a]芘(BP)的大鼠,N-乙酰半胱氨酸(NAC)对其肝脏和肺具有显著的保护作用。由于德弗洛拉等人采用的实验方案,BP在骨髓微核试验中无活性,因此,无法评估NAC在该组织中的潜在保护作用。在本研究中,连续三天每日给予7,12-二甲基苯并蒽(DMBA;通过口服灌胃给予15或25毫克/千克/天),在最后一剂给药24小时后,雄性C57BL/6小鼠骨髓中微核多染红细胞(MPE)数量出现预期增加。在每次给予DMBA前5小时,用NAC(通过口服灌胃给予1克/千克/天)对相似组小鼠进行预处理,对MPE频率没有影响。得出的结论是,NAC对小鼠骨髓没有保护作用。