GENETIC TOXICITY OF 6 CARCINOGENS AND 6 NONCARCINOGENS IN THE DROSOPHILA WING SPOT-TEST

被引:42
作者
TRIPATHY, NK
WURGLER, FE
FREI, H
机构
[1] SWISS FED INST TECHNOL,INST TOXICOL,CH-8092 ZURICH,SWITZERLAND
[2] UNIV ZURICH,CH-8006 ZURICH,SWITZERLAND
来源
MUTATION RESEARCH | 1990年 / 242卷 / 03期
关键词
2-Aminobiphenyl; 4-Aminobiphenyl; Amitrole; Ascorbic acid; Chlorambucil; Drosophila; Mannitol; Melphalan; Piperonyl butoxide; SMART; Sodium arsenate; Sodium arsenite; Stannous chloride; Titanium dioxide; Wing spot test;
D O I
10.1016/0165-1218(90)90082-D
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Six rodent carcinogens, 5 of which are also human carcinogens, and 6 compounds recognized as non-carcinogens were tested for their genotoxic activity in the Drosophila melanogaster wing spot test. 72-h-old larvae trans-heterozygous for the recessive wing cell markers 'multiple wing hairs' (mwh) and 'flare' (flr3) were fed various concentrations of the test compounds for a period of 48 h. With amitrole and 4-aminobiphenyl, larvae of the same age were also given an acute treatment of 6 h with higher concentrations, and, in addition, 48-h-old larvae were fed for a longer period of 72 h. Repeats of all experiments document the good reproducibility of the results in the wing spot test. Amitrole and 4-aminobiphenyl were genotoxic after both 48-h and 72-h treatments, but their activity could not be detected following acute exposure of only 6 h. Chlorambucil and melphalan were clearly genotoxic. The carcinogens sodium arsenite and sodium arsenate, however, which are highly toxic to Drosophila, could only be tested at low exposure levels and were negative undere these treatment conditions. The 6 non-carcinogens (ascorbic acid, 2-aminobiphenyl, mannitol, piperonyl butoxide, stannous chloride and titanium dioxide) were all definitely non-genotoxic in the Drosophila wing spot test. The data for the non-carcinogens demonstrate that non-genotoxic compounds can be identified in the wing spot test with a reasonable experimental effort. © 1990.
引用
收藏
页码:169 / 180
页数:12
相关论文
共 48 条
[31]   CHEMICALS SHOWING NO EVIDENCE OF CARCINOGENICITY IN LONG-TERM, 2-SPECIES RODENT STUDIES - THE NEED FOR SHORT-TERM TEST DATA [J].
SHELBY, MD ;
STASIEWICZ, S .
ENVIRONMENTAL MUTAGENESIS, 1984, 6 (06) :871-878
[32]  
SIMMON VF, 1979, J NATL CANCER I, V62, P911
[33]   INDUCTION OF REVERSE MUTATION AND MITOTIC GENE CONVERSION BY SOME METAL-COMPOUNDS IN SACCHAROMYCES-CEREVISIAE [J].
SINGH, I .
MUTATION RESEARCH, 1983, 117 (1-2) :149-152
[34]   THE SCE-INDUCING CAPACITY OF VITAMIN-C - INVESTIGATIONS INVITRO AND INVIVO [J].
SPEIT, G ;
WOLF, M ;
VOGEL, W .
MUTATION RESEARCH, 1980, 78 (03) :273-278
[35]   NEED FOR A MAMMALIAN TEST SYSTEM FOR MUTAGENS - ACTION OF SOME REDUCING AGENTS [J].
STICH, HF ;
WEI, L ;
LAM, P .
CANCER LETTERS, 1978, 5 (04) :199-204
[36]   MUTAGENIC ACTION OF ASCORBIC-ACID [J].
STICH, HF ;
KARIM, J ;
KOROPATNICK, J ;
LO, L .
NATURE, 1976, 260 (5553) :722-724
[37]   CHEMICAL MUTAGENESIS TESTING IN DROSOPHILA .3. RESULTS OF 48 CODED COMPOUNDS TESTED FOR THE NATIONAL TOXICOLOGY PROGRAM [J].
VALENCIA, R ;
MASON, JM ;
WOODRUFF, RC ;
ZIMMERING, S .
ENVIRONMENTAL MUTAGENESIS, 1985, 7 (03) :325-348
[39]  
Wurgler F. E., 1985, PROGR MUTATION RES, V5, P325
[40]  
WURGLER FE, 1986, CHEM MUTAGENS, V10, P1