Sjöberg P, Bondesson U, Gustafsson J
Department of Drugs, National Board of Health and Welfare, Uppsala, Sweden.
Biol Neonate. 1988;53(1):32-8. doi: 10.1159/000242759.
The aim of the investigation was to study to what extent maturity influences the metabolism of mono-(2-ethylhexyl)phthalate (MEHP), the primary metabolite of the plasticizer di-(2-ethylhexyl)phthalate. The conversion of MEHP to its (omega-1)-hydroxylated product was determined in liver microsomes from fetal, neonatal (1- and 5-day-old) and adult rats. Product formation was determined by gas chromatography-mass spectrometry. The results show that fetal and neonatal as well as adult rat livers are capable of metabolizing MEHP by (omega-1)-hydroxylation. Preparations from 1- and 5-day-old rats were much more efficient than those from fetal rats. The transition into adult life gave no further increase in hydroxylase activity as compared to that in 5-day-old rats. The work shows that there is a rapid postnatal development of MEHP (omega-1)-hydroxylase activity in the rat.
该研究的目的是探究成熟度对邻苯二甲酸二(2-乙基己基)酯的主要代谢产物单(2-乙基己基)邻苯二甲酸酯(MEHP)代谢的影响程度。在来自胎儿、新生(1日龄和5日龄)及成年大鼠的肝脏微粒体中测定MEHP向其(ω-1)-羟基化产物的转化。通过气相色谱-质谱法测定产物形成。结果表明,胎儿、新生及成年大鼠的肝脏均能够通过(ω-1)-羟基化代谢MEHP。1日龄和5日龄大鼠的制剂比胎儿大鼠的制剂效率高得多。与5日龄大鼠相比,成年后的羟化酶活性没有进一步增加。该研究表明,大鼠出生后MEHP(ω-1)-羟化酶活性有快速发展。