Engelhardt G, Fleig H
Department of Toxicology, BASF Aktiengesellschaft, Ludwigshafen, Germany.
Mutat Res. 1993 Jan;298(3):149-55. doi: 10.1016/0165-1218(93)90035-c.
1-Methyl-2-pyrrolidinone induces aneuploidy in yeast, but only under special treatment conditions. Other genotoxic effects have not been found in vitro, and in vivo no data are available in the literature. Therefore, NMP was investigated in the mouse micronucleus test and the Chinese hamster bone marrow test for structural and numerical chromosomal aberrations. These tests can detect both types of alterations as demonstrated by appropriate positive control substances (cyclophosphamide, vincristine sulfate and benomyl). NMP at single oral doses up to 3800 mg/kg body weight (approximately 80% of the LD50) did not lead to an increase either in micronucleated erythrocytes or in structural or numerical chromosomal aberrations when bone marrow was sampled 16, 24 and 48 h after treatment in the micronucleus test or after 24 and 48 h for karyotype analysis.
1-甲基-2-吡咯烷酮可诱导酵母出现非整倍体,但仅在特殊处理条件下。体外未发现其他遗传毒性作用,且文献中尚无体内相关数据。因此,在小鼠微核试验和中国仓鼠骨髓试验中对NMP进行了结构和数量染色体畸变研究。如适当的阳性对照物质(环磷酰胺、硫酸长春新碱和苯菌灵)所示,这些试验可检测到两种类型的改变。在微核试验中,处理后16、24和48小时采集骨髓,或在处理后24和48小时进行核型分析时,单次口服剂量高达3800mg/kg体重(约为半数致死量的80%)的NMP,并未导致微核红细胞数量增加,也未导致结构或数量染色体畸变增加。