Sal'nikova L E, Bakhitova L M, Pashin Iu V
Biull Eksp Biol Med. 1988 Jan;105(1):66-7.
Genetic effects of alkylation alone and combined with carbamoylation were studied following treatment of CHO-AT3-2 Chinese hamster cell line with N-nitroso-N-methylurea for 7 and 60 min. Gene mutations at HGPRT and Na+/K+-ATPase loci, micronuclei, cells with fragmented nuclei and lethality caused by NMU were recorded. Prolonged exposure to the mutagen made these effects more pronounced, particularly the fragmented nuclei and cell death. The combined action of the two mechanisms, therefore, enhanced the mutagenic effects of alkylation and expanded the range of DNA lesions towards greater incidence of gross damage to chromosomes and chromatids.
在用N-亚硝基-N-甲基脲处理中国仓鼠CHO-AT3-2细胞系7分钟和60分钟后,研究了单独烷基化以及烷基化与氨甲酰化联合作用的遗传效应。记录了次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HGPRT)和钠钾ATP酶位点的基因突变、微核、核碎片化细胞以及由N-亚硝基-N-甲基脲引起的致死率。长时间暴露于诱变剂会使这些效应更加明显,尤其是核碎片化和细胞死亡。因此,这两种机制的联合作用增强了烷基化的诱变效应,并扩大了DNA损伤范围,导致染色体和染色单体出现更严重损伤的发生率更高。