Aneuploidy induced by dimethylarsinic acid in mouse bone marrow cells

被引:31
作者
Kashiwada, E [1 ]
Kuroda, K [1 ]
Endo, G [1 ]
机构
[1] Osaka City Univ, Sch Med, Dept Prevent Med & Environm Hlth, Abeno Ku, Osaka 545, Japan
关键词
dimethylarsinic acid; aneuploidy; mouse bone marrow; cytogenetic assay; cell cycle progression;
D O I
10.1016/S1383-5718(98)00011-4
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
We investigated the cytogenetic effects of dimethylarsinic acid (DMA), which is the major metabolite of inorganic arsenic compounds, on mouse bone marrow cells after a single intraperitoneal injection to mice. DMA increased mitotic indices significantly at 16, 24 and 48 h after injection, and prolonged the average generation time 1.5 h at the: 24 h. These results suggest that DMA may cause mitotic arl est in vivo as well as in vitro. However the activity of mitotic arrest induced by DMA was much weaker than that induced by colchicine. Metaphase cells obtained after administration of DMA without colchicine pretreatment were morphologically normal except for chromosome number, which varied by stage fi-om the prophase to the telophase in M phase as seen after administration of saline. DMA significantly induced aneuploids. The frequencies of euploids with DMA and saline treatment were 55.1 and 94.0%, respectively, and in DMA treatment hyperploids with or 2 extra chromosomes were over 80% of all aneuploids. These results suggest that aneuploidy induced by DMA might be associated with carcinogenicity of arsenic. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:33 / 38
页数:6
相关论文
共 22 条
[1]   STUDY OF FACTORS INFLUENCING THE INVIVO METHYLATION OF INORGANIC ARSENIC IN RATS [J].
BUCHET, JP ;
LAUWERYS, R .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1987, 91 (01) :65-74
[2]   Metabolites of arsenic induced tetraploids and mitotic arrest in cultured cells [J].
Eguchi, N ;
Kuroda, K ;
Endo, G .
ARCHIVES OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 1997, 32 (02) :141-145
[3]  
ENDO G, 1992, B ENVIRON CONTAM TOX, V48, P131
[4]   Induction of hypoploidy and cell cycle delay by acrylamide in somatic and germinal cells of male mice [J].
Gassner, P ;
Adler, ID .
MUTATION RESEARCH-GENETIC TOXICOLOGY, 1996, 367 (04) :195-202
[5]   THE INDUCTION OF MICRONUCLEI AS A MEASURE OF GENOTOXICITY - A REPORT OF THE UNITED-STATES ENVIRONMENTAL-PROTECTION-AGENCY GENE-TOX PROGRAM [J].
HEDDLE, JA ;
HITE, M ;
KIRKHART, B ;
MAVOURNIN, K ;
MACGREGOR, JT ;
NEWELL, GW ;
SALAMONE, MF .
MUTATION RESEARCH, 1983, 123 (01) :61-118
[6]  
IARC (International Agency for Research on Cancer), 1987, MONOGRAPHS EVALUATIO, P100
[7]  
Iwami K, 1997, APPL ORGANOMET CHEM, V11, P743, DOI 10.1002/(SICI)1099-0739(199709)11:9<743::AID-AOC642>3.0.CO
[8]  
2-Q
[9]   INDUCTION OF ANEUPLOIDY BY MITOTIC ARRESTANTS IN MOUSE BONE-MARROW [J].
LIANG, JC ;
SATYAPRAKASH, KL .
MUTATION RESEARCH, 1985, 155 (1-2) :61-70
[10]   ORIGIN OF ANEUPLOIDY IN RELATION TO DISTURBANCES OF CELL-CYCLE PROGRESSION .1. EFFECTS OF VINBLASTINE ON MOUSE BONE-MARROW CELLS [J].
MANCA, A ;
BASSANI, B ;
RUSSO, A ;
PACCHIEROTTI, F .
MUTATION RESEARCH, 1990, 229 (01) :29-36