Brambilla G, Cavanna M, Parodi S, Sciaba L, Pino A, Robbiano L
Int J Cancer. 1978 Aug 15;22(2):174-80. doi: 10.1002/ijc.2910220211.
DNA single-strand breaks induced in various organs of BALB/c mice by treatment with a single dose of 1,2-dimethylhydrazine (DMH) were studied by means of the alkaline elution method modified in order to allow the evaluation of DNA damage in vivo with no need of radioactive prelabelling. DNA damage was detected in liver, lung, kidney, stomach and colon mucosa, with the liver showing the greatest amount of damage. Its degree was dependent on the dose and route of administration. A differential effect was evident in colon mucosa from Swiss and C57BL/6 mice which are respectively susceptible and resistant to the induction of bowel tumors by DMH. The higher degree of DNA damage found in liver in comparison with colon mucosa is consistent with the previously reported higher degree of DNA methylation, but does not correlate with the specificity of this carcinogen in inducing tumors of the large intestine in mice given repeated subcutaneous injections.
采用改良的碱性洗脱法研究了单剂量1,2 - 二甲基肼(DMH)处理后BALB/c小鼠各器官中诱导产生的DNA单链断裂情况,该改良方法无需放射性预标记即可在体内评估DNA损伤。在肝脏、肺、肾、胃和结肠黏膜中均检测到DNA损伤,其中肝脏的损伤量最大。其损伤程度取决于给药剂量和途径。在分别对DMH诱导肠肿瘤敏感和耐药的瑞士小鼠和C57BL/6小鼠的结肠黏膜中,明显存在差异效应。与结肠黏膜相比,肝脏中发现的较高程度的DNA损伤与先前报道的较高程度的DNA甲基化一致,但与该致癌物在给小鼠反复皮下注射时诱导大肠肿瘤的特异性无关。