Mutat Res. 1992 Feb-Mar;278(2-3):83-98.
The main goal of the Collaborative Study Group for the Micronucleus Test (CSGMT) was to validate a new method for the micronucleus test, recently introduced by Hayashi et al. (1990), using mouse peripheral blood cells stained supravitally with acridine orange (AO). The micronucleus tests were performed on CD-1 mice using 23 chemicals with various modes of action. As a rule, one chemical was studied by two participants. Peripheral blood sampled from the same animal was examined 0, 24, 48, and 72 h (or longer) after treatment. The frequencies of micronucleated peripheral reticulocytes (MNRETs) were recorded based on observation of 1000 reticulocytes per mouse. All chemicals induced MNRETs dose-dependently. Interlaboratory differences in the induction of MNRETs were in an acceptable range for most chemicals tested. Although differences were observed with some chemicals, there were no discrepancies in qualitative judgment. Most chemicals gave the greatest response 48 h after treatment, which was less variable than in the bone marrow assay (greatest response, 24-48 h). These results suggest that the peripheral blood assay using the AO supravital staining technique generates reproducible and reliable data to evaluate the clastogenicity of chemicals. This makes the peripheral blood micronucleus assay an attractive alternative to the conventional bone marrow assay.
微核试验协作研究组(CSGMT)的主要目标是验证一种新的微核试验方法,该方法由Hayashi等人于1990年提出,使用吖啶橙(AO)对小鼠外周血细胞进行活体染色。使用23种具有不同作用方式的化学物质对CD-1小鼠进行微核试验。通常,每种化学物质由两名参与者进行研究。在处理后0、24、48和72小时(或更长时间)对来自同一只动物的外周血进行检查。根据每只小鼠观察1000个网织红细胞的结果记录微核化外周网织红细胞(MNRET)的频率。所有化学物质均剂量依赖性地诱导MNRET。对于大多数测试的化学物质,实验室间MNRET诱导差异在可接受范围内。虽然观察到某些化学物质存在差异,但在定性判断上没有分歧。大多数化学物质在处理后48小时产生最大反应,其变异性低于骨髓试验(最大反应在24 - 48小时)。这些结果表明,使用AO活体染色技术的外周血试验能够产生可重复且可靠的数据来评估化学物质的致断裂性。这使得外周血微核试验成为传统骨髓试验的一个有吸引力的替代方法。