Testing of p-dichlorobenzene and hexachlorobenzene for their ability to induce DNA damage and micronucleus formation in primary cultures of rat and human hepatocytes

被引:31
作者
Canonero, R [1 ]
Campart, GB [1 ]
Mattioli, F [1 ]
Robbiano, L [1 ]
Martelli, A [1 ]
机构
[1] UNIV GENOA,IST FARMACOL,I-16132 GENOA,ITALY
关键词
D O I
10.1093/mutage/12.1.35
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
The genotoxicity of p-dichlorobenzene (DCB) and hexachlorobenzene (HCB) was evaluated in primary cultures of rat and human hepatocytes, DNA fragmentation was measured by the alkaline elution technique and clastogenic activity by the increase in micronucleus formation, In rat hepatocytes, exposure to concentrations of DCB ranging from 0.56 to 3.2 mM and of HCB from 0.1 to 0.56 mM did not induce any significant increase in the frequency of DNA breaks but consistently produced a statistically significant increase in the frequency of micronucleated cells, In human hepatocytes, under the same experimental conditions, the response to DCB was negative in terms of both DNA fragmentation and clastogenic effect, whereas HCB produced a significant increase in the frequency of both DNA breaks and micronuclei, Taken as a whole these results suggest that of the two pesticides examined only HCB should be considered as a weak genotoxic carcinogen.
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页码:35 / 39
页数:5
相关论文
共 35 条
[1]
LONG-TERM TOXICITY OF HEXACHLOROBENZENE IN THE RAT AND THE EFFECT OF DIETARY VITAMIN-A [J].
ARNOLD, DL ;
MOODIE, CA ;
CHARBONNEAU, SM ;
GRICE, HC ;
MCGUIRE, PF ;
BRYCE, FR ;
COLLINS, BT ;
ZAWIDZKA, ZZ ;
KREWSKI, DR ;
NERA, EA ;
MUNRO, IC .
FOOD AND CHEMICAL TOXICOLOGY, 1985, 23 (09) :779-793
[2]
STRUCTURE ACTIVITY RELATIONSHIP (SAR) MODELS ESTABLISHED INVITRO WITH THE NEUTRAL RED CYTOTOXICITY ASSAY [J].
BABICH, H ;
BORENFREUND, E .
TOXICOLOGY IN VITRO, 1987, 1 (01) :3-9
[3]
MAINTENANCE OF THE BIOTRANSFORMATION CAPACITY BY CULTURED HUMAN HEPATOCYTES AFTER SEVERAL DAILY EXPOSURES TO DRUGS [J].
BEGUE, JM ;
KOCH, P ;
MAURER, G ;
GUILLOUZO, A .
TOXICOLOGY IN VITRO, 1993, 7 (04) :493-498
[4]
LIMITATIONS OF METABOLIC-ACTIVATION SYSTEMS USED WITH INVITRO TESTS FOR CARCINOGENS [J].
BIGGER, CAH ;
TOMASZEWSKI, JE ;
DIPPLE, A ;
LAKE, RS .
SCIENCE, 1980, 209 (4455) :503-505
[5]
GENOTOXICITY OF N-NITROSOCHLORDIAZEPOXIDE IN CULTURED MAMMALIAN-CELLS [J].
BRAMBILLA, G ;
ROBBIANO, L ;
MARTELLI, A ;
CAJELLI, E ;
ALLAVENA, A ;
MAZZEI, M .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1989, 97 (03) :480-488
[6]
CABRAL JRP, 1978, TOXICOL APPL PHARM, V45, P323
[7]
CARCINOGENIC ACTIVITY OF HEXACHOLOROBENZENE IN HAMSTERS [J].
CABRAL, JRP ;
SHUBIK, P ;
MOLLNER, T ;
RAITANO, F .
NATURE, 1977, 269 (5628) :510-511
[8]
CARCINOGENESIS OF HEXACHLOROBENZENE IN MICE [J].
CABRAL, JRP ;
MOLLNER, T ;
RAITANO, F ;
SHUBIK, P .
INTERNATIONAL JOURNAL OF CANCER, 1979, 23 (01) :47-51
[9]
IMPROVED MICRO-FLUOROMETRIC DNA DETERMINATION IN BIOLOGICAL-MATERIAL USING 33258-HOECHST [J].
CESARONE, CF ;
BOLOGNESI, C ;
SANTI, L .
ANALYTICAL BIOCHEMISTRY, 1979, 100 (01) :188-197
[10]
ERTURK E, 1986, IARC SCI PUBL, V77, P417