Nitro musk compounds - Genotoxic activity - Genotoxicity testing of nitro musks with the SOS-chromotest and the sister-chromatid exchange test

被引:14
作者
Kevekordes, S
Grahl, K
Zaulig, A
Dunkelberg, H
机构
[1] Med. Inst. Gen. Hyg. Environ. Hlth., Universität of Göttingen, D-37073 Göttingen
关键词
nitro musks; musk xylene; musk ketone; musk ambrette; musk moskene; musk tibetene; genotoxicity; SOS chromotest; sister-chromatid exchange test; human lymphocytes;
D O I
10.1007/BF02986953
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Five nitro musk compounds are widely used as fragrance ingredients in perfumes, lotions and detergents; as food additives in cigarettes and fish baits, and in such technical products as herbicide formulations and explosives. Several studies identified nitro musk compounds in aquatic environment samples, human milk and fat samples as highly lipophilic and persistent bioaccumulating environmental pollutants. To examine the compounds for genotoxic activity, musk xylene (1-tert.-butyl-3,5-dimethyl-2,4,6-trinitrobenzene), musk ketone (4-tert.-butyl-3,5-dinitro-2,6-dimethylacetophenone), musk ambrette (1-tert.-butyl-4-methyl-6-methoxy-3,5-dinitrobenzene), musk moskene (1,1,3,3,5-pentamethyl-4,6-di-nitroindane) and musk tibetene (1-tert.-butyl-3,4,5-trimethyl-2,6-dinitrobenzene) were rested for SOS inducing potency in the SOS chromotest with E. coli PQ37 and for sister-chromatid exchange inducing activities in human lymphocytes in vitro both in the presence and absence of an exogenous metabolizing system from rat liver S9-Mix. Nitro musks revealed no genotoxicity either in the SOS chromotest with E. coli PQ37 or in the sister-chromatid exchange rest with human lymphocytes.
引用
收藏
页码:189 / 192
页数:4
相关论文
共 33 条
[1]   A comparative study of five nitro musk compounds for genotoxicity in the SOS chromotest and Salmonella mutagenicity [J].
Emig, M ;
Reinhardt, A ;
MerschSundermann, V .
TOXICOLOGY LETTERS, 1996, 85 (03) :151-156
[2]   THE SOS CHROMOTEST, A COLORIMETRIC ASSAY BASED ON THE PRIMARY CELLULAR-RESPONSES TO GENOTOXIC AGENTS [J].
HOFNUNG, M ;
QUILLARDET, P .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1988, 534 :817-825
[3]  
HOFNUNG M, 1989, NEW TRENDS GENETIC R, P125
[4]  
IWATA N, 1993, EUR J PHARM-ENVIRON, V248, P243
[5]   CELL-KINETICS AND SISTER-CHROMATID-EXCHANGE FREQUENCY IN HUMAN-LYMPHOCYTES [J].
LAMBERTI, L ;
PONZETTO, PB ;
ARDITO, G .
MUTATION RESEARCH, 1983, 120 (2-3) :193-199
[6]   MICROFLUOROMETRIC DETECTION OF DEOXYRIBONUCLEIC-ACID REPLICATION IN HUMAN METAPHASE CHROMOSOMES [J].
LATT, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (12) :3395-3399
[7]   MUSK XYLENE INDUCES AND INHIBITS MOUSE HEPATIC CYTOCHROME-P-450 2B ENZYMES [J].
LEHMANMCKEEMAN, LD ;
CAUDILL, D ;
YOUNG, JA ;
DIERCKMAN, TA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 206 (03) :975-980
[8]  
Liebl B, 1993, Gesundheitswesen, V55, P527
[9]   LONG-TERM TOXICITY CARCINOGENICITY OF MUSK XYLOL IN B6C3F1 MICE [J].
MAEKAWA, A ;
MATSUSHIMA, Y ;
ONODERA, H ;
SHIBUTANI, M ;
OGASAWARA, H ;
KODAMA, Y ;
KUROKAWA, Y ;
HAYASHI, Y .
FOOD AND CHEMICAL TOXICOLOGY, 1990, 28 (08) :581-586
[10]  
Mersch-Sundermann Volker, 1995, Anticancer Research, V15, P1653