Induction of cytochrome P450 activities in Drosophila melanogaster strains susceptible or resistant, to insecticides

被引:27
作者
Amichot, M
Brun, A
Cuany, A
De Souza, G
Le Mouél, T
Bride, JM
Babault, M
Salaün, JP
Rahmani, R
Bergé, JB
机构
[1] INRA, LBI, Unite Rech Resistance Xenobiot, F-06606 Antibes, France
[2] CNRS, UA 1182, F-67083 Strasbourg, France
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY | 1998年 / 121卷 / 1-3期
关键词
Drosophila melanogaster; cytochrome P450; induction; insecticide; resistance; hydroxylation; testosterone; lauric acid; ethoxycoumarin; ethoxyresorufin;
D O I
10.1016/S0742-8413(98)10052-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We analysed Drosophila melanogaster cytochrome P450's (P450) through the measurements of four enzymatic activities: ethoxycoumarin-O-deethylase, ethoxyresorufin-O-deethylase, lauric acid hydroxylation, and testosterone hydroxylation. We did these measurements in two Drosophila strains: one is susceptible to insecticides (Canton(S)) and the other is resistant to insecticides by enhanced P450 activities (RDDTR). In addition, we also treated the flies with eight chemicals (beta-naphtoflavone, benzo-alpha-pyrene, 3-methylcholanthrene, phenobarbital, aminopyrine, rifampicin, prochloraz, and clofibrate) known to induce genes from the families CYP1, CYP2, CYP3, CYP4, and CYP6. Metabolisation of all the substrates by P450 from flies microsomes was observed. The chemicals had different effects on these activities, ranging from induction to inhibition. The effects of these chemicals varied with the strains as most of them were ineffective on the RDDTR strain. The results showed that P450-dependent activities are numerous in Drosophila. Regulation features of these activities are complex. The availability of mutant strains as RDDTR should allow fundamental studies of P450 in insects. (C) 1998 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:311 / 319
页数:9
相关论文
共 65 条
[1]   Protection by coffee against somatic genotoxicity in Drosophila: Role of bioactivation capacity [J].
Abraham, SK ;
Graf, U .
FOOD AND CHEMICAL TOXICOLOGY, 1996, 34 (01) :1-14
[2]  
AMICHOT M, 1994, CYTOCHROME P450, P689
[3]  
AMICHOT M, 1995, X86026 GENB
[4]   EXPRESSION OF HOUSE-FLY CYP6A1 AND NADPH-CYTOCHROME P450 REDUCTASE IN ESCHERICHIA-COLI AND RECONSTITUTION OF AN INSECTICIDE-METABOLIZING P450 SYSTEM [J].
ANDERSEN, JF ;
UTERMOHLEN, JG ;
FEYEREISEN, R .
BIOCHEMISTRY, 1994, 33 (08) :2171-2177
[5]   PHOTOAFFINITY-LABELING OF METHYL FARNESOATE EPOXIDASE IN COCKROACH CORPORA ALLATA [J].
ANDERSEN, JF ;
CERUSO, M ;
UNNITHAN, GC ;
KUWANO, E ;
PRESTWICH, GD ;
FEYEREISEN, R .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 25 (06) :713-719
[6]  
BACH J, 1989, XENOBIOTICA, V19, P1
[7]  
BASETT MH, 1996, U44753 GENB
[8]   CYTOCHROME-P450 FAMILY-4 IN A COCKROACH - MOLECULAR-CLONING AND REGULATION BY HYPERTREHALOSEMIC HORMONE [J].
BRADFIELD, JY ;
LEE, YH ;
KEELEY, LL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (10) :4558-4562
[9]   Inducibility of the Drosophila melanogaster cytochrome P450 gene, CYP6A2, by phenobarbital in insecticide susceptible or resistant strains [J].
Brun, A ;
Cuany, A ;
LeMouel, T ;
Berge, J ;
Amichot, M .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1996, 26 (07) :697-703
[10]  
BURKE MD, 1974, DRUG METAB DISPOS, V2, P583