Cox R, Irving C C
Cancer Res. 1976 Nov;36(11 Pt 1):4114-8.
Bladder cancer can be induced in the rat by the intravesicular administration of N-methyl-N-nitrosourea. DNA damage in rat bladder epithelial cells after administration of methylnitrosourea has been examined by measuring the change in sedimentation of the DNA in alkaline sucrose gradients. A dose response of DNA damage in the urothelium was observed with single intravesicular doses of 0.1, 0.3, and 0.5 mg of methylnitrosourea. Larger doses of methylnitrosourea damaged the epithelium so extensively, that biochemical studies were not feasible. DNA repair, measured by the return to a normal sedimentation pattern of DNA on alkaline sucrose gradients, was followed over a period of 9 days with the use of 0.5 mg of methylnitrosourea to initiate the damage. Bladder epithelial cells were able to repair the DNA damage induced by methylnitrosourea. However, the possibility of persistent damage not detectable by sedimentation of DNA on alkaline sucrose gradients cannot be ruled out.
通过膀胱内给予N-甲基-N-亚硝基脲可在大鼠中诱发膀胱癌。通过测量碱性蔗糖梯度中DNA沉降的变化,已检测了给予甲基亚硝基脲后大鼠膀胱上皮细胞中的DNA损伤。单次膀胱内给予0.1、0.3和0.5mg甲基亚硝基脲时,观察到尿路上皮中DNA损伤的剂量反应。更大剂量的甲基亚硝基脲对上皮造成了广泛损伤,以至于无法进行生化研究。使用0.5mg甲基亚硝基脲引发损伤后,在9天的时间里跟踪通过碱性蔗糖梯度上DNA恢复正常沉降模式来测量的DNA修复情况。膀胱上皮细胞能够修复由甲基亚硝基脲诱导的DNA损伤。然而,不能排除存在通过碱性蔗糖梯度上DNA沉降无法检测到的持续性损伤的可能性。