Renner H W, Wever J
Food Chem Toxicol. 1983 Apr;21(2):123-7. doi: 10.1016/0278-6915(83)90225-9.
Chinese hamsters and mice were made sulphite-oxidase deficient by the feeding of a low-molybdenum diet with sodium tungstate as a drinking-water supplement. Hepatic sulphite-oxidase activity was checked spectrophotometrically. Under normal conditions, sulphite-oxidase activity is high in the mouse and low in the Chinese hamster. Sulphite (SO3--) was given in a single or double oral dose in aqueous solution or dissolved in fruit juice or by repeated subcutaneous injections up to the maximum tolerated doses. Possible cytogenetic effects were studied in bone-marrow cells using three test systems--the sister chromatid exchange, chromosome aberration and micronucleus tests. No induction of cytogenetic effects was observed with any of the three tests in either species, indicating that no damage at the chromosomal level was induced by sulphite in these animals, even when sulphite-oxidase activity was reduced to a very low level.
通过给中国仓鼠和小鼠喂食低钼饮食并在饮水中添加钨酸钠,使其亚硫酸盐氧化酶缺乏。用分光光度法检测肝脏亚硫酸盐氧化酶活性。在正常情况下,小鼠的亚硫酸盐氧化酶活性高,而中国仓鼠的活性低。亚硫酸盐(SO3--)以单次或双次口服剂量的水溶液形式给予,或溶解在果汁中,或通过重复皮下注射直至最大耐受剂量。使用三种测试系统——姐妹染色单体交换、染色体畸变和微核试验,研究了骨髓细胞中可能的细胞遗传学效应。在这两个物种中,三种测试中的任何一种都未观察到细胞遗传学效应的诱导,这表明即使亚硫酸盐氧化酶活性降低到非常低的水平,亚硫酸盐在这些动物中也不会诱导染色体水平的损伤。