Edwards G, Whong W Z, Speciner N
Mutat Res. 1979 Dec;64(6):415-23. doi: 10.1016/0165-1161(79)90111-0.
An intrahepatic host-mediated mutagenicity assay capable of detecting low levels of N-nitrosomorpholine (NMOR) is described. The indicator organism was Salmonella typhimurium TA1530 which had been injected intravenously 10 min prior to the administration of the test compound. The bacteria were subsequently recovered from the liver and scored for revertants by standard methods. The lower limit of detectibility of this system for intubated NMOR was 0.2 microgram/g body weight. This assay was then used to study the formation of NMOR in vivo from morpholine and nitrite which had been sequentially gavaged to mice. Under acidic conditions (pH 3.4) 12--19% of the administered morpholine was converted to NMOR in the presence of excess nitrite. This nitrosation, and the subsequent uptake and activation of the NMOR, took place so rapidly that most of the total mutagenic response was complete within 15 min. This response was inhibited by prior intubation of ascorbic acid, a known inhibitor of nitrosation, and enhanced by sodium thiocyanate, a nitrosation catalyst.
本文描述了一种能够检测低水平N-亚硝基吗啉(NMOR)的肝内宿主介导的致突变性试验。指示生物为鼠伤寒沙门氏菌TA1530,在给予受试化合物前10分钟经静脉注射。随后从肝脏中回收细菌,并通过标准方法对回复突变体进行计数。该系统对经插管给予的NMOR的可检测下限为0.2微克/克体重。然后使用该试验研究了对小鼠依次灌胃给予吗啉和亚硝酸盐后体内NMOR的形成。在酸性条件(pH 3.4)下,在过量亚硝酸盐存在的情况下,所给予吗啉的12%-19%转化为NMOR。这种亚硝化作用以及随后NMOR的摄取和活化发生得非常迅速,以至于大部分总致突变反应在15分钟内就完成了。已知的亚硝化作用抑制剂抗坏血酸预先插管可抑制这种反应,而亚硝化作用催化剂硫氰酸钠则可增强这种反应。