Aitio A, Parkki M
Arch Int Pharmacodyn Ther. 1978 Oct;235(2):187-95.
Dibutyl-, di(2-ethylhexyl)-, di(3, 3, 5-trimethylhexyl)- and didecylphthalate (DBP, DEHP, TMHP, DDP) all caused an increase in the amount of hepatic cytochrome P=450, when administered intragastrically to rats. No statistically significant increase could be detected in the catalytic activities dependent on cytochrome P-450 (Benzo(a)pyrene hydroxylation, ethoxycoumarin deethylation). Dibutylphthalate inhibited these reactions, when added to the incubation in vitro. Phthalates caused an increase in the activities of epoxide hydratase, and glutathione-S-transferase. Conjugation of 0-aminophenol and 4-methylumbelliferone with glucuronic acid was increased after phthalate administration.
将邻苯二甲酸二丁酯、二(2-乙基己基)酯、二(3,3,5-三甲基己基)酯和二癸酯(DBP、DEHP、TMHP、DDP)经胃内给予大鼠后,均会导致肝脏细胞色素P-450含量增加。在依赖细胞色素P-450的催化活性(苯并(a)芘羟基化、乙氧基香豆素脱乙基作用)方面未检测到统计学上的显著增加。当在体外孵育中添加邻苯二甲酸二丁酯时,它会抑制这些反应。邻苯二甲酸酯会导致环氧化物水解酶和谷胱甘肽-S-转移酶的活性增加。给予邻苯二甲酸酯后,0-氨基酚和4-甲基伞形酮与葡糖醛酸的结合增加。