CLASTOGENIC EFFECTS OF KNOWN AND SUSPECT SPINDLE POISONS STUDIED BY CHROMOSOME ANALYSIS IN MOUSE BONE-MARROW CELLS

被引:53
作者
WANG, X
ADLER, ID
机构
[1] GESELL STRAHLEN & UMWELTFORSCH MBH, INST SAUGETIERGENET, W-8042 NEUHERBERG, GERMANY
[2] YUNNAN NORMAL UNIV, DEPT BIOL, YUNNAN, PEOPLES R CHINA
关键词
D O I
10.1093/mutage/5.4.371
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The present study was performed within the project 'Genomic Mutations' (sponsored by the Commission of the European Communities) in order to gather all possible experimental information on 10 chemicals selected on the basis of their possible capacity to induce aneuploidy. An analysis of chromosomal aberrations was carried out in bone marrow cells of mice with the first five chemicals: colchicine (COL), econazole (EZ), chloralhydrate (CH), hydroquinone (HQ) and diazepam (DIAZ). The experiments were performed in parallel to micronucleus tests with the objective to distinguish a positive micronucleus response due to chromosomal breakage from that obtained by lagging chromosomes. The results of the micronucleus tests will be reported elsewhere. COL, CH, EZ and DIAZ showed on clastogenic effects in mouse bone marrow cells after single intraperitoneal injection. Polyploid cells were significantly more frequent after COL treatment. HQ showed a dose-dependent induction of chromosomal aberrations at 6 and 24 h after treatment. After 24 h, cells with multiple aberrations up to complete chromosome fragmentation were frequently observed. They indicate that a small fraction of the cell population, probably related to a specific stage of the cell cycle, was particularly sensitive to HQ. A sex difference in clastogenic response to HQ was not observed. It is concluded that of the five chemicals tested only HQ was clastogenic in mouse bone marrow cells under the present experimental conditions. © 1990 Oxford University Press.
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页码:371 / 374
页数:4
相关论文
共 27 条
[1]  
Adler I.-D., 1984, MUTAGENICITY TESTING, P275
[2]  
ADLER ID, 1989, IN PRESS MUTAT RES
[3]   BENZENE INDUCES MICRONUCLEI IN CIRCULATING ERYTHROCYTES OF CHRONICALLY TREATED MICE [J].
BARALE, R ;
GIORGELLI, F ;
MIGLIORE, L ;
CIRANNI, R ;
CASINI, D ;
ZUCCONI, D ;
LOPRIENO, N .
MUTATION RESEARCH, 1985, 144 (03) :193-196
[4]   MEMBRANE-DAMAGING AGENTS CAUSE MITOTIC NONDISJUNCTION IN ASPERGILLUS-NIDULANS [J].
BELLINCAMPI, D ;
GUALANDI, G ;
LAMONICA, E ;
POLEY, C ;
MORPURGO, GP .
MUTATION RESEARCH, 1980, 79 (02) :169-172
[5]   MUTAGENIC ACTIVITY OF 61 AGENTS AS DETERMINED BY THE MICRONUCLEUS, SALMONELLA, AND SPERM ABNORMALITY ASSAYS [J].
BRUCE, WR ;
HEDDLE, JA .
CANADIAN JOURNAL OF GENETICS AND CYTOLOGY, 1979, 21 (03) :319-333
[6]   BENZENE AND THE GENOTOXICITY OF ITS METABOLITES .1. TRANS-PLACENTAL ACTIVITY IN MOUSE FETUSES AND IN THEIR DAMS [J].
CIRANNI, R ;
BARALE, R ;
MARRAZZINI, A ;
LOPRIENO, N .
MUTATION RESEARCH, 1988, 208 (01) :61-67
[7]   BENZENE AND THE GENOTOXICITY OF ITS METABOLITES .2. THE EFFECT OF THE ROUTE OF ADMINISTRATION ON THE MICRONUCLEI AND BONE-MARROW DEPRESSION IN MOUSE BONE-MARROW CELLS [J].
CIRANNI, R ;
BARALE, R ;
GHELARDINI, G ;
LOPRIENO, N .
MUTATION RESEARCH, 1988, 209 (1-2) :23-28
[8]   RECENT FINDINGS ON THE GENETIC TOXICOLOGY OF BENZENE, TOLUENE, XYLENES AND PHENOLS [J].
DEAN, BJ .
MUTATION RESEARCH, 1985, 154 (03) :153-181
[9]   DIFFERENCE BETWEEN INTRAPERITONEAL AND ORAL GAVAGE APPLICATION IN THE MICRONUCLEUS TEST - THE 3RD COLLABORATIVE STUDY BY CSGMT JEMS MMS [J].
HAYASHI, M ;
SUTOU, S ;
SHIMADA, H ;
SATO, S ;
SASAKI, YF ;
WAKATA, A .
MUTATION RESEARCH, 1989, 223 (04) :329-344
[10]  
HUS TC, 1983, MUTAT RES, V122, P201