Clozel M, Beharry K, Aranda J V
Biol Neonate. 1986;50(2):83-90. doi: 10.1159/000242572.
Indomethacin is now widely used during the neonatal period, but few data exist concerning its metabolism during this period. Thus, we studied the maturational changes in the metabolism of indomethacin into desmethylindomethacin by isolated liver microsomes from 1- to 60-day-old rats. From 8 days of age on, there was a progressive increase in enzymatic activity which was inversely correlated with the change in Michaelis-Menten constant. However, the maximal velocity was not significantly affected by the age. These findings suggest that the deficient metabolism of indomethacin in the newborn rat is due to decreased affinity between enzyme and substrate, or presence of competitive inhibitors. To determine the substrate specificity of the monooxygenase-catalyzing inducers, sodium phenobarbital and beta-naphthoflavone given during 3 days in neonatal rats were also studied. Although beta-naphthoflavone did not exhibit any significant effect, phenobarbital significantly increased the activity and maximal velocity of indomethacin O-demethylation.
吲哚美辛目前在新生儿期广泛使用,但关于其在此期间的代谢情况数据较少。因此,我们利用1至60日龄大鼠的离体肝微粒体研究了吲哚美辛代谢为去甲基吲哚美辛过程中的成熟变化。从8日龄开始,酶活性逐渐增加,这与米氏常数的变化呈负相关。然而,最大反应速度并未受到年龄的显著影响。这些发现表明,新生大鼠中吲哚美辛代谢不足是由于酶与底物之间的亲和力降低,或存在竞争性抑制剂。为了确定催化诱导剂的单加氧酶的底物特异性,我们还研究了在新生大鼠出生后3天内给予苯巴比妥钠和β-萘黄酮的情况。虽然β-萘黄酮未表现出任何显著影响,但苯巴比妥显著提高了吲哚美辛O-去甲基化的活性和最大反应速度。