Evaluation of the genotoxic activity of metronidazole and dimetridazole in human lymphocytes by the comet assay

被引:75
作者
Re, JL
DeMeo, MP
Laget, M
Guiraud, H
Castegnaro, M
Vanelle, P
Dumenil, G
机构
[1] FAC PHARM MARSEILLE,LAB BIOGENOTOXICOL & MUTAGENESE ENVIRONM EA 1784,F-13385 MARSEILLE 5,FRANCE
[2] INT AGCY RES CANC,UNITE CANCEROL ENVIRONM EA 1784,F-69372 LYON 8,FRANCE
[3] FAC PHARM MARSEILLE,CHIM ORGAN LAB,F-13385 MARSEILLE 5,FRANCE
关键词
metronidazole; dimetridazole; 8-hydroxyquinoline; vitamin C; catalase; superoxide dismutase; comet assay; DNA damage; lymphocyte; human;
D O I
10.1016/S0027-5107(97)00010-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The genotoxicity of metronidazole (MZ) and dimetridazole (DZ) has been evaluated in human lymphocytes using the comet assay. The test has been performed using 3 doses (58.4, 175.2 and 292.1 mu M for MZ; and 70.9, 212.6 and 354.3 mu M for DZ) under 3 experimental protocols: aerobiosis, anaerobiosis (90% N-2, 10% CO2) and with the presence of the microsomal fraction S9 mix. The effects of 4 antioxidants (8-hydroxyquinoline (8HQ), vitamin C (VitC), catalase (CAT) and superoxide dismutase (SOD), have been investigated on DNA damage generated by fixed concentrations of MZ (292.1 mu M) and DZ (354.4 mu M). In aerobic conditions, MZ and DZ produced significant dose-response relationships. The dose-related effects of both drugs decreased or were abolished in anaerobic conditions or in presence of S9 mix. 8HQ, VitC, CAT and SOD induced dose-related protective responses against DNA damage due to MZ and DZ, These findings suggest that MZ and DZ induce DNA damage in human lymphocytes through the futile cycle, The one-electron reduction of the drugs leads to the production of nitro radical anions. In the presence of oxygen, these radicals are reoxidized and generate oxygen-activated species.
引用
收藏
页码:147 / 155
页数:9
相关论文
共 45 条
[21]   DOES PHYSICAL-ACTIVITY INDUCE DNA-DAMAGE [J].
HARTMANN, A ;
PLAPPERT, U ;
RADDATZ, K ;
GRUNERTFUCHS, M ;
SPEIT, G .
MUTAGENESIS, 1994, 9 (03) :269-272
[22]  
HEIMBROOK DC, 1985, MOL PHARMACOL, V29, P168
[23]   DIMETHYLSULFOXIDE AS MODIFIER OF THE ORGANOSPECIFIC MUTAGENICITY OF METRONIDAZOLE IN MICE [J].
HRELIA, P ;
SCOTTI, M ;
MOROTTI, M ;
VIGAGNI, F ;
PAOLINI, M ;
SAPIGNI, E ;
CANTELLIFORTI, G .
TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS, 1990, 10 (03) :263-271
[24]  
HRELIA P, 1987, MUAGENESIS, V2, P45
[25]   THE METABOLIC-ACTIVATION OF NITROHETEROCYCLIC THERAPEUTIC AGENTS [J].
KEDDERIS, GL ;
MIWA, GT .
DRUG METABOLISM REVIEWS, 1988, 19 (01) :33-62
[26]   THE MUTAGENICITY OF NITROAROMATIC DRUGS - EFFECT OF METRONIDAZOLE AFTER INCUBATION IN HYPOXIA INVITRO [J].
KORBELIK, M ;
HORVAT, D .
MUTATION RESEARCH, 1980, 78 (02) :201-207
[27]   THE EFFECTS OF METRONIDAZOLE ON THE FREQUENCY OF SISTER-CHROMATID EXCHANGES AND CHROMOSOMAL-ABERRATIONS IN HUMAN-LYMPHOCYTES INVITRO AND INVIVO [J].
LAMBERT, B ;
LINDBLAD, A .
MUTATION RESEARCH, 1980, 74 (03) :230-230
[28]  
LARUSSO NF, 1977, MOL PHARMACOL, V13, P872
[29]  
LOFT S, 1990, PHARM TOXICOL S6, V66, P331
[30]   VALIDITY OF INVITRO TESTING [J].
MATULA, TI .
DRUG METABOLISM REVIEWS, 1990, 22 (6-8) :777-787