Mackenzie P I, Väisänen M, Hänninen O
Toxicol Lett. 1982 Aug;12(4):259-63. doi: 10.1016/0378-4274(82)90249-1.
Administration of the carcinogens, benzo[a]pyrene and 1,2-benzanthracene, increased UDP glucuronosyltransferase activities towards 4-nitrophenol, 3-hydroxybenzo[a]pyrene, 7-hydroxycoumarin and 1-naphthol to a greater extent than did pretreatment with the noncarcinogens, anthracene and phenanthrene. However, the activity towards morphine was preferentially increased by the noncarcinogens. Activities towards testosterone and oestrone were only slightly increased by the four hydrocarbons. The results suggest that even within a single class of inducer various compounds are capable of causing a differential stimulation of UDP glucuronosyltransferase activities towards certain substrates.
给予致癌物苯并[a]芘和1,2-苯并蒽后,相较于用非致癌物蒽和菲预处理,UDP葡萄糖醛酸基转移酶对4-硝基苯酚、3-羟基苯并[a]芘、7-羟基香豆素和1-萘酚的活性有更大程度的增加。然而,非致癌物优先增加了对吗啡的活性。这四种碳氢化合物对睾酮和雌酮的活性仅有轻微增加。结果表明,即使在单一类别的诱导剂中,各种化合物对某些底物的UDP葡萄糖醛酸基转移酶活性也能产生不同的刺激作用。