Inducing effect of phenobarbital on clozapine metabolism in patients with chronic schizophrenia

被引:22
作者
Facciola, G
Avenoso, A
Spina, E
Perucca, E
机构
[1] Univ Messina, Inst Pharmacol, I-98122 Messina, Italy
[2] Azienda USL 5, Ctr Mental Hlth, Messina, Italy
[3] Univ Pavia, Dept Internal Med, Clin Pharmacol Unit, Ctr Mental Hlth, I-27100 Pavia, Italy
关键词
phenobarbital; clozapine; norclozapine; clozapine N-oxide; drug interaction; enzyme induction;
D O I
10.1097/00007691-199812000-00008
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The steady state plasma concentrations of clozapine and its two major metabolites, norclozapine and clozapine N-oxide, were compared in patients with schizophrenia treated with clozapine in combination with phenobarbital (n = 7), and in control patients treated with clozapine alone (n = 15). Patients were matched for sex, age, body weight, and antipsychotic dosage. Patients comedicated with phenobarbital had significantly lower plasma clozapine levels than those of the controls (232 +/- 104 versus 356 +/- 138 ng/ml; mean, SD, p < 0.05). Plasma norclozapine levels did not differ between the two groups (195 +/- 91 versus 172 +/- 61 ng/ml, NS), whereas clozapine N-oxide levels were significantly higher in the phenobarbital group (115 +/- 49 versus 53 +/- 31 ng/ml, p < 0.01). Norclozapine/clozapine and clozapine N-oxide/clozapine ratios were also significantly higher (p < 0.001) in patients comedicated with phenobarbital. These findings suggest that phenobarbital stimulates the metabolism of clozapine, probably by inducing its N-oxidation and demethylation pathways.
引用
收藏
页码:628 / 630
页数:3
相关论文
共 18 条
[1]   Determination of clozapine, desmethylclozapine and clozapine N-oxide in human plasma by reversed-phase high-performance liquid chromatography with ultraviolet detection [J].
Avenoso, A ;
Facciolá, G ;
Campo, GM ;
Fazio, A ;
Spina, E .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 1998, 714 (02) :299-308
[2]  
BALDESSARINI RJ, 1991, NEW ENGL J MED, V324, P746
[3]   CLOZAPINE DISPOSITION COVARIES WITH CYP1A2 ACTIVITY DETERMINED BY A CAFFEINE TEST [J].
BERTILSSON, L ;
CARRILLO, JA ;
DAHL, ML ;
LLERENA, A ;
ALM, C ;
BONDESSON, U ;
LINDSTROM, L ;
DELARUBIA, IR ;
RAMOS, S ;
BENITEZ, J .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1994, 38 (05) :471-473
[4]   FLUVOXAMINE IS A POTENT INHIBITOR OF CYTOCHROME-P4501A2 [J].
BROSEN, K ;
SKJELBO, E ;
RASMUSSEN, BB ;
POULSEN, HE ;
LOFT, S .
BIOCHEMICAL PHARMACOLOGY, 1993, 45 (06) :1211-1214
[5]  
Edge SC, 1997, HUM PSYCHOPHARM CLIN, V12, P5, DOI 10.1002/(SICI)1099-1077(199701/02)12:1<5::AID-HUP831>3.0.CO
[6]  
2-4
[7]   The involvement of CYP1A2 and CYP3A4 in the metabolism of clozapine [J].
Eiermann, B ;
Engel, G ;
Johansson, I ;
Zanger, UM ;
Bertilsson, L .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1997, 44 (05) :439-446
[8]   Will routine therapeutic drug monitoring have a place in clozapine therapy? [J].
Freeman, DJ ;
Oyewumi, LK .
CLINICAL PHARMACOKINETICS, 1997, 32 (02) :93-100
[9]  
HARING C, 1990, AM J PSYCHIAT, V147, P1471
[10]  
HIEMKE C, 1994, J CLIN PSYCHOPHARM, V14, P279