Hakura A, Mochida H, Yamatsu K
Department of Drug Safety Research, Eisai Co., Ltd., Ibaraki, Japan.
Mutat Res. 1993 Nov;303(3):127-33. doi: 10.1016/0165-7992(93)90025-q.
We used the Ames method with the modification of pre-incubation to evaluate the potential mutagenicity of DMSO. We performed the assays using nine different Ames Salmonella strains and Escherichia coli strains WP2 and WP2uvrA. DMSO was found to be mutagenic for Salmonella typhimurium TA1537 and TA2637 (the latter strain being isogenic to TA1537 but carrying plasmid pKM101) and for E. coli WP2uvrA. The mutagenic activity of DMSO observed at a concentration of 33% was about 10 times higher than the background level (65 revertants induced) for TA1537 after 20 min of incubation, where some lethal toxicity was observed. The mutagenicity of DMSO was observed in the presence and absence of rat liver S9 mix.
我们采用预孵育改良的艾姆斯试验法来评估二甲基亚砜(DMSO)的潜在致突变性。我们使用九种不同的艾姆斯沙门氏菌菌株以及大肠杆菌WP2和WP2uvrA菌株进行了检测。结果发现,DMSO对鼠伤寒沙门氏菌TA1537和TA2637(后者与TA1537基因同源,但携带质粒pKM101)以及大肠杆菌WP2uvrA具有致突变性。在33%的浓度下观察到,DMSO的致突变活性比TA1537在孵育20分钟后的背景水平(诱导65个回复突变体)高约10倍,此时观察到了一些致死毒性。无论有无大鼠肝脏S9混合液,均观察到了DMSO的致突变性。