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异喹胍表型对普萘洛尔代谢诱导性的影响。

Influence of debrisoquin phenotype on the inducibility of propranolol metabolism.

作者信息

Shaheen O, Biollaz J, Koshakji R P, Wilkinson G R, Wood A J

机构信息

Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN 37232.

出版信息

Clin Pharmacol Ther. 1989 Apr;45(4):439-43. doi: 10.1038/clpt.1989.52.

Abstract

The effects of rifampin (600 mg) once daily for 22 days on the total and fractional metabolic clearances of propranolol were determined in a group of six genetically extensive (EM) and six poor metabolizers (PM) of debrisoquin. The impaired ability of PMs to metabolize propranolol to the ring-oxidized metabolite 4-hydroxypropranolol was confirmed. The total oral clearance of propranolol increased about fourfold in both phenotypes from 219.2 +/- 52.8 to 976.7 L/hr in the EMs and from 75.0 +/- 12.6 to 289.8 +/- 78.2 L/hr in the PMs. The extent of induction of glucuronidation was similar in the two groups. 4-Hydroxylation was induced in both phenotypes but the increase was fifteenfold greater in EMs than in PMs. This would imply that the cytochrome P-450 determined by the debrisoquin allele or some coinherited 4-hydroxylase(s) was induced to a greater extent in EMs than PMs.

摘要

在一组6名异喹胍基因广泛代谢者(EM)和6名异喹胍代谢不良者(PM)中,测定了每日一次服用利福平(600毫克),持续22天对普萘洛尔总代谢清除率和分数代谢清除率的影响。证实了PM代谢普萘洛尔生成环氧化代谢物4-羟基普萘洛尔的能力受损。普萘洛尔的口服总清除率在两种表型中均增加了约四倍,在EM中从219.2±52.8升/小时增至976.7升/小时,在PM中从75.0±12.6升/小时增至289.8±78.2升/小时。两组中葡萄糖醛酸化的诱导程度相似。两种表型中4-羟基化均被诱导,但EM中的增加幅度比PM中的大15倍。这意味着由异喹胍等位基因或某些共同遗传的4-羟化酶所决定的细胞色素P-450在EM中比在PM中诱导程度更大。

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