CONTRIBUTION OF CYTOCHROME P450S TO MEOS (MICROSOMAL ETHANOL-OXIDIZING SYSTEM) - A SPECIFIC AND SENSITIVE ASSAY OF MEOS ACTIVITY BY HPLC WITH FLUORESCENCE LABELING

被引：30

作者：

KUNITOH, S ^{[1
]}

TANAKA, T ^{[1
]}

IMAOKA, S ^{[1
]}

FUNAE, Y ^{[1
]}

MONNA, Y ^{[1
]}

机构：

[1] OSAKA CITY UNIV,SCH MED,CHEM LAB,ABENO KU,OSAKA 545,JAPAN

来源：

ALCOHOL AND ALCOHOLISM | 1993年 / 28卷

关键词：

D O I：

10.1093/alcalc/28.Supplement_1B.63

中图分类号：

R194 [卫生标准、卫生检查、医药管理];

学科分类号：

摘要：

The contribution of cytochrome P450s to MEOS (microsomal ethanol-oxidizing system) in rat hepatic microsomes was studied with a modified assay method for MEOS activity. Acetaldehyde produced by MEOS was coverted into the fluorescent derivative with cyclohexane-1,3-dione and analyzed by HPLC with a fluorescence detector. Acetaldehyde production by hepatic microsomes of rats treated with ethanol was higher by 75% than that by control rats. Ethanol oxidation activity of eight forms of P450 was investigated in a reconstituted system. CYP1A2 and CYP2E1 had high rates of acetaldehyde formation. The K-m value of CYP2E1 for ethanol oxidation was 9.48 mM, similar to that of hepatic microsomes from rats treated with ethanol. The K-m value of CYP1A2 was higher than that of CYP2E1, indicating the CYP1A2 with lower affinity for ethanol compared with CYP2E1. From the results of an inhibition study with antibodies, CYP2E1 was found to be a main contributor to MEOS induced by ethanol in rats, but CYP1A2 was considered to play an important role for MEOS when CYP2E1 was not induced. These results present the possibility that CYP1A2 and CYP2E1 contribute to MEOS activity.

引用

页码：63 / 68

页数：6

共 26 条

[1] FATTY LIVER IN RAT AFTER PROLONGED INTAKE OF ETHANOL WITH A NUTRITIONALLY ADEQUATE NEW LIQUID DIET [J].

DECARLI, LM ;

LIEBER, CS .

JOURNAL OF NUTRITION, 1967, 91 (3P1) :331-&

[2] COMPARATIVE EFFECTS OF ETHANOL ADMINISTRATION ON HEPATIC MONOOXYGENASES IN RATS AND MICE [J].

ELVES, RG ;

UENG, TH ;

ALVARES, AP .

ARCHIVES OF TOXICOLOGY, 1984, 55 (04) :258-264

[3] PURIFICATION AND CHARACTERIZATION OF LIVER MICROSOMAL CYTOCHROME-P-450 FROM UNTREATED MALE-RATS [J].

FUNAE, Y ;

IMAOKA, S .

BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 926 (03) :349-358

[4] SIMULTANEOUS PURIFICATION OF MULTIPLE FORMS OF RAT-LIVER MICROSOMAL CYTOCHROME-P-450 BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].

FUNAE, Y ;

IMAOKA, S .

BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 842 (2-3) :119-132

[5]

FUNAE Y, 1993, HDB EXPT PHARM, V105, P221

[6] ENZYMATIC PRODUCTION OF ACETALDEHYDE FROM ETHANOL IN RAT-BRAIN TISSUE [J].

GILL, K ;

MENEZ, JF ;

LUCAS, D ;

DEITRICH, RA .

ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1992, 16 (05) :910-915

[7] PURIFICATION AND CHARACTERIZATION OF 2 CONSTITUTIVE CYTOCHROME-P-450 (F1 AND F2) FROM ADULT FEMALE RATS - IDENTIFICATION OF P-450F-1 AS THE PHENOBARBITAL-INDUCIBLE CYTOCHROME-P-450 IN MALE-RAT LIVER [J].

IMAOKA, S ;

TERANO, Y ;

FUNAE, Y .

BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 916 (03) :358-367

[8] ETHANOL-INDUCIBLE, FASTING-INDUCIBLE, AND ACETONE-INDUCIBLE CYTOCHROMES-P-450 IN RAT-LIVER - REGULATION AND CHARACTERISTICS OF ENZYMES BELONGING TO THE IIB-GENE AND IIE-GENE SUBFAMILIES [J].

JOHANSSON, I ;

EKSTROM, G ;

SCHOLTE, B ;

PUZYCKI, D ;

JORNVALL, H ;

INGELMANSUNDBERG, M .

BIOCHEMISTRY, 1988, 27 (06) :1925-1934

[9]

KAMATAKI T, 1983, MOL PHARMACOL, V24, P146

[10] N-HYDROXYLATION OF CARCINOGENIC AND MUTAGENIC AROMATIC-AMINES [J].

KATO, R ;

KAMATAKI, T ;

YAMAZOE, Y .

ENVIRONMENTAL HEALTH PERSPECTIVES, 1983, 49 (MAR) :21-25

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