Pletsa V, Steenwinkel M J, van Delft J H, Baan R A, Kyrtopoulos S A
Laboratory of Chemical Carcinogenesis, Institute of Biological Research and Biotechnology, National Hellenic Research Foundation, Athens, Greece.
Cancer Lett. 1999 Jan 8;135(1):21-7. doi: 10.1016/s0304-3835(98)00262-6.
Following single or multiple oral treatments of rats or lambda lacZ transgenic mice with methyl bromide, methylated DNA adducts (N7- and/or O6-methylguanine) were found at comparable levels in various tissues, including among others the glandular stomach, the forestomach and the liver. Multiple rat treatment resulted in substantial decreases in the repair enzyme O6-alkylguanine-DNA alkyltransferase which were probably due in part to direct interaction of the enzyme with methyl bromide. However, no induction of mutagenesis in the lacZ transgene could be detected in any tissue 14 days after single treatments of up to 50 mg/kg or after multiple treatments of as many as 10 daily treatments of 25 mg/kg MeBr.
用溴甲烷对大鼠或λ-乳糖操纵子转基因小鼠进行单次或多次口服处理后,在包括腺胃、前胃和肝脏等多种组织中发现了甲基化DNA加合物(N7-和/或O6-甲基鸟嘌呤),且水平相当。对大鼠进行多次处理导致修复酶O6-烷基鸟嘌呤-DNA烷基转移酶大幅减少,这可能部分归因于该酶与溴甲烷的直接相互作用。然而,在单次给予高达50 mg/kg或多次给予多达10次每日25 mg/kg溴甲烷处理后的14天,在任何组织中均未检测到lacZ转基因的诱变。