Morrison J B, Hecht S S
IARC Sci Publ. 1984(57):185-92.
A sensitive method was developed for quantitation of N-nitrosomorpholine (NMOR) formation in vivo in rats. A major metabolite of NMOR, N-nitroso(2-hydroxyethyl)glycine, was detected by gas chromatography-thermal energy analysis in the urine of rats treated with trace levels of NMOR or treated sequentially with morpholine and sodium nitrite. Since significant levels of 2-hydroxyethylglycine do not seem to occur in rat urine, even after treatment with morpholine, artefact formation was not a problem. Formation of 1 micrograms NMOR in vivo was readily detected. The formation of NMOR from morpholine and sodium nitrite in vivo in rats appeared to depend on the doses of morpholine and [sodium nitrite]2 and occurred in higher yield than reported for formation of N-nitrosoproline, as expected. The formation of NMOR from morpholine and sodium nitrite under the conditions of the carcinogenicity study of Shank and Newberne was quantified. The daily levels of NMOR formation were highly variable, but the mean level was consistent with the tumorigenicity data in that dose-response study.
已开发出一种灵敏的方法来定量大鼠体内N-亚硝基吗啉(NMOR)的形成。通过气相色谱-热能分析在经痕量NMOR处理或先后用吗啉和亚硝酸钠处理的大鼠尿液中检测到了NMOR的一种主要代谢产物N-亚硝基(2-羟乙基)甘氨酸。由于即使在用吗啉处理后大鼠尿液中似乎也不会出现大量的2-羟乙基甘氨酸,因此假象的形成不是一个问题。在体内形成1微克NMOR很容易被检测到。大鼠体内由吗啉和亚硝酸钠形成NMOR的过程似乎取决于吗啉和[亚硝酸钠]2的剂量,并且正如预期的那样,其产率高于报道的N-亚硝基脯氨酸的形成产率。在Shank和Newberne的致癌性研究条件下,对由吗啉和亚硝酸钠形成NMOR的过程进行了定量。NMOR形成的每日水平变化很大,但平均水平与该剂量反应研究中的致瘤性数据一致。