Kahl G F, Müller W, Kahl R, Jonen H G, Netter K J
Naunyn Schmiedebergs Arch Pharmacol. 1978 Oct;304(3):297-301. doi: 10.1007/BF00507972.
A differential inhibition of biphenyl hydroxylation by alpha-naphthoflavone and metyrapone was observed in isolated perfused rat liver. alpha-Naphthoflavone inhibited 2- and 4-hydroxylation in livers from beta-naphthoflavone-pretreated animals but had no effect on both reactions in livers from phenobarbital-pretreated animals. Metyrapone inhibited 2- and 4-hydroxylation in phenobarbital-stimulated livers, but only insignificant inhibition of 2-hydroxylation and a slight enhancement of 4-hydroxylation by metyrapone was observed in beta-naphthoflavone-stimulated livers. Conjugation of 2-hydroxybiphenyl and 4-hydroxybiphenyl by isolated perfused livers was also studied. 4-Hydroxybiphenyl preferentially formed sulphates in livers from untreated animals but after induction glucuronidation was as effective as sulphation or even exceeded sulphation. Only glucuronic acid conjugates of 2-hydroxybiphenyl were detected.
在离体灌注大鼠肝脏中观察到α-萘黄酮和甲吡酮对联苯羟基化的差异抑制作用。α-萘黄酮抑制β-萘黄酮预处理动物肝脏中的2-和4-羟基化反应,但对苯巴比妥预处理动物肝脏中的这两种反应均无影响。甲吡酮抑制苯巴比妥刺激肝脏中的2-和4-羟基化反应,但在β-萘黄酮刺激的肝脏中,仅观察到甲吡酮对2-羟基化的抑制作用不显著,对4-羟基化有轻微增强作用。还研究了离体灌注肝脏对2-羟基联苯和4-羟基联苯的结合作用。在未处理动物的肝脏中,4-羟基联苯优先形成硫酸盐,但诱导后葡糖醛酸化与硫酸化效果相当,甚至超过硫酸化。仅检测到2-羟基联苯的葡糖醛酸结合物。