Cytotoxic and genotoxic effects of the azo-dye p-dimethylaminoazobenzene in mice:: A time-course study

被引:27
作者
Biswas, SJ [1 ]
Khuda-Bukhsh, AR [1 ]
机构
[1] Univ Kalyani, Cytogenet Lab, Dept Zool, Kalyani 741235, W Bengal, India
关键词
hepatocarcinogenesis; p-dimethylaminoazobenzene; genotoxicity; tumour marker enzymes;
D O I
10.1016/j.mrgentox.2005.06.011
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
The cytotoxic and genotoxic effects of chronic feeding of the azo-dye p-dimethylaminoazobenzene (p-DAB) during 7, 15, 30, 60, 90 and 120 days have been assessed in mice. The endpoints used for genotoxic analysis were chromosome aberrations (CA), micronuclei (MN) and mitotic index (MI) in bone-marrow cells, and sperm-head abnormality (SHA) in male gonads. The activities of marker enzymes for toxicity, such as glutamate oxalo-acetate transaminase (GOT), glutamate pyruvate transaminase (GPT), acid phosphatase (ACP) and alkaline phosphatase (ALKP) were also assayed periodically, as was lipid peroxidation (LPO). Chronic feeding of p-DAB produced increased numbers of chromosome aberrations, nuclear anomalies and sperm-head abnormalities, as compared with normal untreated controls, generally in a time-dependent manner until 60 days, after which the anomalies persisted, but rather erratically. However, although there was some noticeable modulation in enzyme activities in the corresponding p-DAB-fed mice as well, these were not strictly time-dependent. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 32 条
[21]   CHEMICAL CARCINOGENS - A REVIEW AND ANALYSIS OF THE LITERATURE OF SELECTED CHEMICALS AND THE ESTABLISHMENT OF THE GENE-TOX CARCINOGEN DATABASE - A REPORT OF THE UNITED-STATES-ENVIRONMENTAL-PROTECTION-AGENCY GENE-TOX PROGRAM [J].
NESNOW, S ;
ARGUS, M ;
BERGMAN, H ;
CHU, K ;
FRITH, C ;
HELMES, T ;
MCGAUGHY, R ;
RAY, V ;
SLAGA, TJ ;
TENNANT, R ;
WEISBURGER, E .
MUTATION RESEARCH, 1987, 185 (1-2) :1-195
[22]  
*NTP, 2002, CARC 10TH
[23]   Oxidative DNA damage induced by an N-hydroxy metabolite of carcinogenic 4-dimethylaminoazobenzene [J].
Ohnishi, S ;
Murata, M ;
Degawa, M ;
Kawanishi, S .
JAPANESE JOURNAL OF CANCER RESEARCH, 2001, 92 (01) :23-29
[24]  
PALEKAR SD, 1966, INDIAN J EXP BIOL, V4, P73
[25]  
Plaa G. L., 1991, TOXIC RESPONSES LIVE
[26]   ALKALINE-PHOSPHATASE ACTIVITY AND REGULATION OF GROWTH IN TRANSFORMED MAMMALIAN-CELLS [J].
SELA, BA ;
SACHS, L .
JOURNAL OF CELLULAR PHYSIOLOGY, 1974, 83 (01) :27-34
[27]   Listing occupational carcinogens [J].
Siemiatycki, J ;
Richardson, L ;
Straif, K ;
Latreille, B ;
Lakhani, R ;
Campbell, S ;
Rousseau, MC ;
Boffetta, P .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2004, 112 (15) :1447-1459
[28]  
TIMBRELL JA, 1991, PRINCIPLES BIOCH TOX
[29]   DNA damage induced by red food dyes orally administered to pregnant and male mice [J].
Tsuda, S ;
Murakami, M ;
Matsusaka, N ;
Kano, K ;
Taniguchi, K ;
Sasaki, YF .
TOXICOLOGICAL SCIENCES, 2001, 61 (01) :92-99
[30]   INCREASED SERUM ALANINE AMINOTRANSFERASE ACTIVITY ASSOCIATED WITH MUSCLE NECROSIS IN THE DOG [J].
VALENTINE, BA ;
BLUE, JT ;
SHELLEY, SM ;
COOPER, BJ .
JOURNAL OF VETERINARY INTERNAL MEDICINE, 1990, 4 (03) :140-143