Nishioka H, Nishi K, Kyokane K
Mutat Res. 1981 Oct;85(5):323-33. doi: 10.1016/0165-1161(81)90223-5.
Mutagenicities of AF-2, MNNG, 4NQO, aflatoxin B1, benzo [a] pyrene and Trp-P-1, with or without metabolic activation, were inactivated by treatment with human saliva to a great extent in the Ames test with Salmonella typhimurium test strains TA98 and TA100. Mutagenic activities of quercetin, pyrolysates of beef, salmon and sodium glutamate, and condensate of cigarette smoke were also decreased to some extent by saliva treatment, but no significant effect was found on the activity of MMS and pyrolysate of polypeptone. These effects showed individual variations. The inhibition of AF-2 mutagenicity by saliva varied with temperature in TA100 but not in TA98 cultures. Boiled saliva inactivated AF-2 mutagenicity in TA98 to some extent but not in TA100 cultures. Inactivation of AF-2 mutagenicity by saliva treatment was completed within 30 sec. Complex mechanisms may be involved in the inactivation of mutagenicity of carcinogens by saliva, including biochemical reactions with enzymes, vitamins, etc. and/or adsorption with high molecular weight substances in saliva such as proteins, bacterial cells, mucous materials, etc.
在使用鼠伤寒沙门氏菌测试菌株TA98和TA100进行的艾姆斯试验中,AF-2、MNNG、4NQO、黄曲霉毒素B1、苯并[a]芘和Trp-P-1在有或无代谢激活的情况下,经人唾液处理后其致突变性在很大程度上被灭活。槲皮素、牛肉、三文鱼和谷氨酸钠的热解产物以及香烟烟雾冷凝物的致突变活性经唾液处理后也有一定程度降低,但对甲磺酸甲酯和蛋白胨热解产物的活性未发现显著影响。这些影响存在个体差异。唾液对AF-2致突变性的抑制在TA100培养物中随温度变化,而在TA98培养物中则不然。煮沸的唾液在一定程度上使TA98中的AF-2致突变性失活,但在TA100培养物中则没有。唾液处理使AF-2致突变性失活在30秒内完成。唾液使致癌物致突变性失活可能涉及复杂机制,包括与酶、维生素等的生化反应和/或与唾液中如蛋白质、细菌细胞、黏液物质等高分子量物质的吸附作用。