Detection of in vivo genotoxicity of 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX) by the alkaline single cell gel electrophoresis (Comet) assay in multiple mouse organs

被引:45
作者
Sasaki, YF
Nishidate, E
Izumiyama, F
WatanabeAkanuma, M
Kinae, N
Matsusaka, N
Tsuda, S
机构
[1] INST ENVIRONM TOXICOL,KODAIRA,TOKYO 187,JAPAN
[2] UNIV SHIZUOKA,SCH FOOD & NUTR SCI,LAB FOOD HYG,SHIZUOKA 422,JAPAN
[3] IWATE UNIV,FAC AGR,DEPT VET MED,LAB VET PUBL HLTH,MORIOKA,IWATE 020,JAPAN
关键词
single cell gel electrophoresis (SCG) assay; comet assay; genotoxicity; multiple organs; mouse; stomach; intestine; bladder; MX;
D O I
10.1016/S1383-5718(97)00085-5
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 tested the genotoxicity of 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanose (MX) in the mouse in 6 organs (liver, lung, kidney, brain, spleen, and bone marrow) and in the mucosa of stomach, jejunum, ileum, colon, and bladder using the alkaline single-cell gel electrophoresis (SCG) (Comet) assay modified by us. Mice were sacrificed 1, 3, 6, and 24 h after oral administration of the mutagen at 100 mg/kg. MX yielded statistically significant DNA damage in the liver, kidney, lung, and brain and in all the mucosa samples. While DNA damage persisted in the gastrointestinal and urinary tract for 6-24 h after a single oral dosing, it peaked in the liver at 1 h and returned to almost the control level at 3 h. Our present results suggest that MX is genotoxic for various mouse organs, but not for the hematopoietic system, and that the alkaline SCG assay with a homogenization technique can be used to predict genotoxicity in the gastrointestinal and urinary tracts. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:47 / 53
页数:7
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