Tsuda H, Miyata Y, Hagiwara A, Hasegawa R, Shirai T, Ito N
Gan. 1977 Dec;68(6):781-3.
N-Butyl-N-(4-hydroxybutyl) nitrosamine (BBN), which selectively induced urinary bladder tumors in several experimental animal species, was found to cause damage of DNA in the bladder epithelium. Wistar strain rats were given 100 mg/kg of BBN intravesically and killed after 2, 6, 12, 24, or 48 hr. DNA damage was examined by measuring the change in sedimentation pattern in an alkaline sucrose gradient. Amount of DNA in each fraction was determined by fluorescence spectrophotometry. At 2 hr, the sedimentation profile shifted from heavier (No 15, control peak) to lighter (Nos. 2 approximately 4) fractions, and the maximum effect appeared at 6 hr as a single peak in the lighter fractions. At 12 hr, damaged DNA was in the process of repair as two peaks were present, one light and one heavy. At 48 hr, the sedimentation profile showed a single peak identical with that of controls indicating complete repair of DNA.
N-丁基-N-(4-羟基丁基)亚硝胺(BBN)能在几种实验动物物种中选择性诱发膀胱肿瘤,已发现它会导致膀胱上皮细胞的DNA损伤。给Wistar品系大鼠膀胱内注射100mg/kg的BBN,并在2、6、12、24或48小时后处死。通过测量碱性蔗糖梯度中沉降模式的变化来检测DNA损伤。用荧光分光光度法测定每个组分中的DNA量。在2小时时,沉降图谱从较重的组分(第15号,对照峰)转移到较轻的组分(第2至4号),最大效应在6小时时出现,表现为较轻组分中的一个单峰。在12小时时,受损DNA处于修复过程中,出现两个峰,一个轻峰和一个重峰。在48小时时,沉降图谱显示出与对照相同的单峰,表明DNA已完全修复。