Evans M A, Papazafiratou C, Bhat R, Vidyasagar D
Pediatr Res. 1981 Nov;15(11):1406-10. doi: 10.1203/00006450-198111000-00003.
Metabolism of indomethacin was examined in freshly isolated hepatocytes prepared by liver collagenase perfusion of fetal (28) and neonatal rabbits of 3, 5, 10, 12, and 25 days of age. Initial cell viability was more than 90% and linear rates of metabolism were observed for up to 2 hr of incubation. Deacylation of indomethacin to desbenzoyl indomethacin showed a rapid increase early in postnatal development while microsomal O-demethylation to desmethyl indomethacin was increased significantly only in the hepatocytes from 25-day-old rabbits. Glucuronide conjugates of indomethacin and indomethacin metabolites accounted for less than 8% of the total metabolites in hepatocytes from 25-day-old rabbits. The maturational development of indomethacin in metabolism may account for previously reported gestational dependent half-life of the drug in the premature infant (9). However, the factors that regulate development of indomethacin metabolism appear to be under more that one control system.
通过对28日龄胎儿以及3、5、10、12和25日龄新生兔进行肝脏胶原酶灌注制备新鲜分离的肝细胞,研究了吲哚美辛的代谢情况。初始细胞活力超过90%,在长达2小时的孵育过程中观察到代谢的线性速率。吲哚美辛脱酰基生成去苯甲酰基吲哚美辛在出生后早期迅速增加,而微粒体O-去甲基化生成去甲基吲哚美辛仅在25日龄兔的肝细胞中显著增加。吲哚美辛及其代谢产物的葡糖醛酸结合物在25日龄兔肝细胞的总代谢产物中占比不到8%。吲哚美辛代谢的成熟发育可能解释了先前报道的该药物在早产儿中的妊娠依赖性半衰期(9)。然而,调节吲哚美辛代谢发育的因素似乎受不止一个控制系统的控制。