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用N-甲基-N-亚硝基脲处理后大鼠食管体内的DNA加合物形成及DNA非预定合成。

DNA adduct formation and unscheduled DNA synthesis in rat esophagus in vivo after treatment with N-methyl-N-nitrosourea.

作者信息

Qin X S, Nakatsuru Y, Kohyama K, Ishikawa T

机构信息

Department of Experimental Pathology, Cancer Institute, Tokyo, Japan.

出版信息

Carcinogenesis. 1990 Feb;11(2):235-8. doi: 10.1093/carcin/11.2.235.

Abstract

An in vivo method for assessment of DNA adduct formation and unscheduled DNA synthesis (UDS) in the esophagus of rats was devised. Small ventral incisions were made in the neck and upper abdomen regions of 6 week old F344 rats and ligation of the esophagus with thread at the two extreme ends performed to make an esophageal pouch. For the DNA adduct formation study, a solution (0.5 ml) containing various concentrations of N-[3H]methyl-N-nitrosourea ([3H]MNU) was injected into the pouch. DNA binding levels were calculated from radioactivity of the isolated DNA and dose-dependent DNA adduct formation could be detected 2 h after the treatment with MNU. By HPLC analysis, both 7-methylguanine (7-mGua) and O6-methylguanine (O6-mGua) adducts were identified in the esophageal DNA, the ratio of 7-mGua/O6-mGua being 5.7-12:1. For UDS measurement, a solution containing MNU plus [3H]thymidine (200 microCi/ml) was similarly injected into the pouch. UDS was dose-dependently demonstrated as silver grains over the nuclei of the epithelial cells by autoradiography. The results thus showed that MNU, when injected into the esophageal lumen, can penetrate the surface mucosa, react with the epithelial cell DNA and induce DNA adduct formation and DNA repair synthesis dose-dependently.

摘要

设计了一种用于评估大鼠食管中DNA加合物形成和非预定DNA合成(UDS)的体内方法。在6周龄的F344大鼠的颈部和上腹部区域做小的腹部切口,并在食管两端用线结扎以形成食管袋。对于DNA加合物形成研究,将含有不同浓度的N-[3H]甲基-N-亚硝基脲([3H]MNU)的溶液(0.5 ml)注入袋中。根据分离的DNA的放射性计算DNA结合水平,在用MNU处理2小时后可检测到剂量依赖性的DNA加合物形成。通过高效液相色谱分析,在食管DNA中鉴定出7-甲基鸟嘌呤(7-mGua)和O6-甲基鸟嘌呤(O6-mGua)加合物,7-mGua/O6-mGua的比例为5.7-12:1。对于UDS测量,将含有MNU加[3H]胸腺嘧啶核苷(200微居里/毫升)的溶液类似地注入袋中。通过放射自显影,UDS表现为上皮细胞核上的银颗粒,呈剂量依赖性。结果表明,当将MNU注入食管腔时,它可以穿透表面粘膜,与上皮细胞DNA反应并剂量依赖性地诱导DNA加合物形成和DNA修复合成。

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