Suzuki E, Mochizuki M, Okada M
Gan. 1981 Oct;72(5):713-6.
The metabolic fate of N-methyl-N-dodecylnitrosamine (MDN) was investigated in the rat, in order to elucidate a possible correlation between urinary metabolites and organotropic carcinogenicity to the urinary bladder of this N-nitrosamine. MDN was extensively metabolized in the rat, no unchanged MDN being found in the urine. The urinary metabolites identified were N-methyl-N-(3-carboxypropyl) nitrosamine (MCPN), N-methyl-N-(2-hydroxy-3-carboxy-propyl) nitrosamine, N-methyl-N-(carboxymethyl) nitrosamine, and N-methyl-N-(2-oxopropyl) nitrosamine. Thus the metabolic pattern of MDN was essentially similar to that of N-methyl-N-(4-hydroxybutyl) nitrosamine, a potent bladder carcinogen, in the rat. A possible important role of MCPN in the induction of bladder tumors by MDN is discussed.
为了阐明尿代谢物与这种N-亚硝胺对膀胱的器官特异性致癌性之间可能存在的相关性,研究了N-甲基-N-十二烷基亚硝胺(MDN)在大鼠体内的代谢命运。MDN在大鼠体内被广泛代谢,尿液中未发现未变化的MDN。鉴定出的尿代谢物为N-甲基-N-(3-羧丙基)亚硝胺(MCPN)、N-甲基-N-(2-羟基-3-羧丙基)亚硝胺、N-甲基-N-(羧甲基)亚硝胺和N-甲基-N-(2-氧代丙基)亚硝胺。因此,MDN的代谢模式与大鼠体内一种强效膀胱致癌物N-甲基-N-(4-羟基丁基)亚硝胺的代谢模式基本相似。讨论了MCPN在MDN诱导膀胱肿瘤中可能起的重要作用。