ANALYSIS OF THE 6 ADDITIONAL CHEMICALS FOR INVITRO ASSAYS OF THE EUROPEAN-ECONOMIC-COMMUNITIES EEC ANEUPLOIDY PROGRAM USING SACCHAROMYCES-CEREVISIAE D61.M AND THE INVITRO PORCINE BRAIN TUBULIN ASSEMBLY ASSAY

被引:9
作者
ALBERTINI, S
BRUNNER, M
WURGLER, FE
机构
[1] SWISS FED INST TECHNOL, INST TOXICOL, CH-8092 ZURICH, SWITZERLAND
[2] UNIV ZURICH, CH-8006 ZURICH, SWITZERLAND
关键词
CHROMOSOMAL MALSEGREGATION; RESISTANT COLONIES; TOXIC DOSES;
D O I
10.1002/em.2850210211
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We tested six additional chemicals (acetaldehyde, benomyl, diethylstilboestrol, diethylstilboestrol dipropionate, griseofulvin, and mercaptoethanol) for in vitro systems of the coordinated programme to study aneuploidy induction sponsored by the Commission of the European Communities in two in vitro test systems. Using Saccharomyces cerevisice D61.M (mitotic chromosomal malsegregation assay), benomyl showed a dose-dependent increase in the frequency of chromosomal malsegregation with a lowest effective dose tested (LEDT) of 30 mug/ml (0.1 mM). Diethylstilboestrol (DES) showed solvent-dependent effects. DES dissolved in ethanol induced an increase in chromosomal malsegregation as well as in the frequency of total resistant colonies (mutations and recombinations) with a LEDT arround 13 mug/ml (0.048 mM). Using dimethylsulfoxide as the solvent, no increases were observed with DES up to 333 mug/ml (1.24 mM). Acetaldehyde induced an increase in chromosomal malsegregation with the cold treatment protocol (LEDT: 1.25 mul/ml (21 mM) and 0.75 mul/ml (13 mM), respectively) but no increase with the overnight protocol (highest dose tested (HDT): 1.75 mul/ml; 30 mM). Concerning the frequency of total cycloheximide-resistant colonies (mutations and recombinations) increases were obtained with both protocols. The other three compounds were negative when tested up to toxic doses (survival below 10%), up to the maximum solubility in the solvent used or up to heavy precipitation in the incubation mix. The HDT were 333 mug/ml (0.88 mM) for diethylstilboestrol dipropionate, 1,600 mug/ml (4.5 mM) for griseofulvin and 0.5 mul/ml (7 mM) for mercaptoethanol. Concerning effects on porcine brain tubulin assembly in vitro, diethylstilboestrol and griseofulvin inhibited the assembly process. The IC30% (30% inhibition concentration) values were 12.5 muM and 100 muM for DES and griseofulvin, respectively. Mercaptoethanol showed no effects up to 50 mM.
引用
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页码:180 / 192
页数:13
相关论文
共 64 条
[1]   MOUSE MICRONUCLEUS TESTS WITH KNOWN AND SUSPECT SPINDLE POISONS - RESULTS FROM 2 LABORATORIES [J].
ADLER, ID ;
KLIESCH, U ;
VANHUMMELEN, P ;
KIRSCHVOLDERS, M .
MUTAGENESIS, 1991, 6 (01) :47-53
[2]   INDUCTION OF MITOTIC CHROMOSOME LOSS IN THE DIPLOID YEAST SACCHAROMYCES-CEREVISIAE D61.M BY GENOTOXIC CARCINOGENS AND TUMOR PROMOTERS [J].
ALBERTINI, S ;
FRIEDERICH, U ;
WURGLER, FE .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1988, 11 (04) :497-508
[3]   INFLUENCE OF DIFFERENT FACTORS ON THE INDUCTION OF CHROMOSOME MALSEGREGATION IN SACCHAROMYCES-CEREVISIAE D61.M BY BAVISTAN AND ASSESSMENT OF ITS GENOTOXIC PROPERTY IN THE AMES TEST AND IN SACCHAROMYCES-CEREVISIAE D7 [J].
ALBERTINI, S .
MUTATION RESEARCH, 1989, 216 (06) :327-340
[4]   REEVALUATION OF THE 9 COMPOUNDS REPORTED CONCLUSIVE POSITIVE IN YEAST SACCHAROMYCES-CEREVISIAE ANEUPLOIDY TEST SYSTEMS BY THE GENE-TOX PROGRAM USING STRAIN D61.M OF SACCHAROMYCES-CEREVISIAE [J].
ALBERTINI, S .
MUTATION RESEARCH, 1991, 260 (02) :165-180
[5]   ANALYSIS OF 9 KNOWN OR SUSPECTED SPINDLE POISONS FOR MITOTIC CHROMOSOME MALSEGREGATION USING SACCHAROMYCES-CEREVISIAE D61.M [J].
ALBERTINI, S .
MUTAGENESIS, 1990, 5 (05) :453-459
[6]   THE DETECTION OF CHEMICALLY-INDUCED CHROMOSOMAL MALSEGREGATION IN SACCHAROMYCES-CEREVISIAE D61.M - A LITERATURE SURVEY (1984-1990) [J].
ALBERTINI, S ;
ZIMMERMANN, FK .
MUTATION RESEARCH, 1991, 258 (03) :237-258
[7]   THE INVITRO PORCINE BRAIN TUBULIN ASSEMBLY ASSAY - EFFECTS OF A GENOTOXIC CARCINOGEN (AFLATOXIN-B1), 8 TUMOR PROMOTERS AND 9 MISCELLANEOUS SUBSTANCES [J].
ALBERTINI, S ;
FRIEDERICH, U ;
HOLDEREGGER, C ;
WURGLER, FE .
MUTATION RESEARCH, 1988, 201 (02) :283-292
[8]  
Baraona E, 1981, Curr Alcohol, V8, P421
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]   EFFECTS OF 10 KNOWN OR SUSPECTED SPINDLE POISONS IN THE INVITRO PORCINE BRAIN TUBULIN ASSEMBLY ASSAY [J].
BRUNNER, M ;
ALBERTINI, S ;
WURGLER, FE .
MUTAGENESIS, 1991, 6 (01) :65-70