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西咪替丁亚硝化物的pH依赖性降解及其机制。

pH-dependent degradation of nitrosocimetidine and its mechanisms.

作者信息

Frank N, Sato S, Tsuda M

机构信息

Biochemistry Division, National Cancer Center Research Institute, Tokyo.

出版信息

Jpn J Cancer Res. 1988 Oct;79(10):1083-8. doi: 10.1111/j.1349-7006.1988.tb01530.x.

Abstract

The degradation of nitrosocimetidine (NC) and its mechanism were found to be strongly dependent upon pH by monitoring NC and its degradation products by high-performance liquid chromatography (HPLC). NC was relatively stable at neutral pH, but it degraded rapidly under both acidic and alkaline conditions. In a strongly acidic solution, the degradation was shown to be entirely by denitrosation, but under alkaline conditions scarcely any denitrosation was observed and various other degradation products were found. At neutral pH, both these degradation mechanisms were observed. In neutral solution, the presence of thiol compounds greatly shortened the half life of NC, and enhanced its denitrosation. The high degradation rate in acidic solution, the strong influence of thiol groups, and the preference of denitrosation at pH 0.3-5 can explain the discrepancy between the in vitro genotoxicity and the lack of carcinogenicity of NC.

摘要

通过高效液相色谱法(HPLC)监测西咪替丁亚硝胺(NC)及其降解产物,发现NC的降解及其机制强烈依赖于pH值。NC在中性pH条件下相对稳定,但在酸性和碱性条件下均迅速降解。在强酸性溶液中,降解完全通过脱亚硝化作用进行,但在碱性条件下几乎未观察到脱亚硝化作用,而是发现了各种其他降解产物。在中性pH条件下,观察到了这两种降解机制。在中性溶液中,硫醇化合物的存在大大缩短了NC的半衰期,并增强了其脱亚硝化作用。酸性溶液中的高降解率、硫醇基团的强烈影响以及在pH 0.3 - 5时脱亚硝化作用的偏好,可以解释NC体外遗传毒性与缺乏致癌性之间的差异。

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Mutation, DNA labeling, and transformation of BHK-21/CL 13 cells by MNNG, and nitrosocimetidine.
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