Cytochrome P450-dependent drug oxidation activities in liver microsomes of various animal species including rats, guinea pigs, dogs, monkeys, and humans

被引:156
作者
Shimada, T [1 ]
Mimura, M [1 ]
Inoue, K [1 ]
Nakamura, S [1 ]
Oda, H [1 ]
Ohmori, S [1 ]
Yamazaki, H [1 ]
机构
[1] CHIBA UNIV HOSP, CHIBA 260, JAPAN
关键词
cytochrome P450; CYP; species; drug metabolism; liver microsomes;
D O I
10.1007/s002040050403
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Levels of cytochrome P450 (P450 or CYP) proteins immunoreactive to antibodies raised against human CYP1A2, 2A6, 2C9, 2E1, and 3A4, monkey CYP2B17, and rat CYP2D1 were determined in liver microsomes of rats, guinea pigs, dogs, monkeys, and humans. We also examined several drug oxidation activities catalyzed by liver microsomes of these animal species using eleven P450 substrates such as phenacetin, coumarin, pentoxyresorufin, phenytoin, S-mephenytoin, bufuralol, aniline, benzphetamine, ethylmorphine, erythromycin, and nifedipine; the activities were compared with the levels of individual P450 enzymes. Monkey liver P450 proteins were found to have relatively similar immunochemical properties by immunoblotting analysis to the human enzymes, which belong to the same P450 gene families. Mean catalytic activities (on basis of mg microsomal protein) of P450-dependent drug oxidations with eleven substrates were higher in liver microsomes of monkeys than of humans, except that humans showed much higher activities for aniline p-hydroxylation than those catalyzed by monkeys. However, when the catalytic activities of liver microsomes of monkeys and humans were compared on the basis of nmol of P450, both species gave relatively similar rates towards the oxidation of phenacetin, coumarin, pentoxyresorufin, phenytoin, mephenytoin, benzphetamine, ethylmorphine, erythromycin, and nifedipine, while the aniline p-hydroxylation was higher and bufuralol 1'-hydroxylation was lower in humans than monkeys. On the other hand: the immunochemical properties of P450 proteins and the activities of P450-dependent drug oxidation reactions in dogs, guinea pigs, and rats were somewhat different from those of monkeys and humans; the differences in these animal species varied with the P450 enzymes examined and the substrates used. The results presented in this study provide useful information towards species-related differences in susceptibilities of various animal species regarding actions and toxicities of drugs and xenobiotic chemicals.
引用
收藏
页码:401 / 408
页数:8
相关论文
共 53 条
[1]   7-ETHOXYCOUMARIN O-DEETHYLASE KINETICS IN ISOLATED RAT, DOG AND HUMAN HEPATOCYTE SUSPENSIONS [J].
BAYLISS, MK ;
BELL, JA ;
WILSON, K ;
PARK, GR .
XENOBIOTICA, 1994, 24 (03) :231-241
[2]   INTERSPECIES VARIATIONS IN CAFFEINE METABOLISM RELATED TO CYTOCHROME-P4501A ENZYMES [J].
BERTHOU, F ;
GUILLOIS, B ;
RICHE, C ;
DREANO, Y ;
JACQZAIGRAIN, E ;
BEAUNE, PH .
XENOBIOTICA, 1992, 22 (06) :671-680
[3]   METABOLISM OF THEOPHYLLINE AND ITS INHIBITION BY FLUOROQUINOLONES IN RAT HEPATIC MICROSOMES [J].
DAVIS, JD ;
AARONS, L ;
HOUSTON, JB .
XENOBIOTICA, 1995, 25 (06) :563-573
[4]  
DISTLERATH LM, 1985, J BIOL CHEM, V260, P9057
[5]  
EBERHART DC, 1991, MOL PHARMACOL, V40, P859
[6]  
GELBOIN HV, 1993, PHARMACOL REV, V45, P413
[7]   ROLE OF HUMAN HEPATIC CYTOCHROMES-P450 IN DRUG-METABOLISM AND TOXICITY [J].
GEORGE, J ;
FARRELL, GC .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1991, 21 (03) :356-362
[8]   BIOCHEMISTRY AND MOLECULAR-BIOLOGY OF THE HUMAN CYP2C SUBFAMILY [J].
GOLDSTEIN, JA ;
DEMORAIS, SMF .
PHARMACOGENETICS, 1994, 4 (06) :285-299
[9]   EVIDENCE THAT CYP2C19 IS THE MAJOR (S)-MEPHENYTOIN 4'-HYDROXYLASE IN HUMANS [J].
GOLDSTEIN, JA ;
FALETTO, MB ;
ROMKESSPARKS, M ;
SULLIVAN, T ;
KITAREEWAN, S ;
RAUCY, JL ;
LASKER, JM ;
GHANAYEM, BI .
BIOCHEMISTRY, 1994, 33 (07) :1743-1752
[10]   ROLE OF HUMAN CYTOCHROMES P450 IN THE METABOLIC-ACTIVATION OF CHEMICAL CARCINOGENS AND TOXINS [J].
GONZALEZ, FJ ;
GELBOIN, HV .
DRUG METABOLISM REVIEWS, 1994, 26 (1-2) :165-183