Wang T, Miller K W, Tu Y Y, Yang C S
J Natl Cancer Inst. 1985 Jun;74(6):1291-7.
The effects of riboflavin deficiency on the metabolism of N-nitrosodimethylamine [(DMN) CAS: 62-75-9] and other nitrosamines were examined in rats. After weanling rats were put on a riboflavin-deficient diet, the development of the deficiency was monitored by the growth rate and the erythrocyte glutathione reductase activation coefficient. In the riboflavin-deficient rats, the liver microsomal NADPH-cytochrome c reductase activity was lower but the cytochrome P450 content was higher than that of the control. The metabolism of DMN was dependent on the severity of the deficiency. During mild deficiency, which was observed mainly with Sprague-Dawley rats, the microsomal DMN demethylase (DMNd) activity was elevated 30-80%, but the metabolism of N-nitrosomethylbenzylamine (CAS: 937-40-6) and three other nitrosamines was slightly decreased. Dietary restriction in the pair-fed group also caused an elevation of DMNd activity above that of the ad libitum control group due to a partial fasting effect. During severe deficiency, which was observed mainly with Wistar rats, however, the metabolism of DMN, as well as the oxidation of benzo[a]pyrene, was decreased. Preincubation with flavin adenine dinucleotide and flavin mononucleotide enhanced the DMNd activity of the microsomes from riboflavin-deficient rats but not that from control rats. The results suggest that, depending on the alterations of the monooxygenase enzyme system during the development of the deficiency, riboflavin deficiencies may have different effects on the metabolism of DMN and some other carcinogens.
研究了核黄素缺乏对大鼠体内N-亚硝基二甲胺[(DMN),化学物质登记号:62-75-9]及其他亚硝胺代谢的影响。将断奶大鼠置于核黄素缺乏饮食环境中后,通过生长速率和红细胞谷胱甘肽还原酶激活系数监测缺乏症的发展情况。在核黄素缺乏的大鼠中,肝脏微粒体NADPH-细胞色素c还原酶活性较低,但细胞色素P450含量高于对照组。DMN的代谢取决于缺乏症的严重程度。在轻度缺乏期间(主要在斯普拉格-道利大鼠中观察到),微粒体DMN脱甲基酶(DMNd)活性提高了30%-80%,但N-亚硝基甲基苄胺(化学物质登记号:937-40-6)及其他三种亚硝胺的代谢略有下降。成对喂养组的饮食限制由于部分禁食效应也导致DMNd活性高于自由进食对照组。然而,在严重缺乏期间(主要在Wistar大鼠中观察到),DMN的代谢以及苯并[a]芘的氧化均下降。用黄素腺嘌呤二核苷酸和黄素单核苷酸预孵育可增强核黄素缺乏大鼠微粒体的DMNd活性,但对对照组大鼠微粒体的DMNd活性无增强作用。结果表明,根据缺乏症发展过程中单一加氧酶系统的变化情况,核黄素缺乏可能对DMN和其他一些致癌物的代谢产生不同影响。