The microcystins-induced DNA damage in the liver and the heart of zebrafish, Danio rerio

被引:4
|
作者
Shahi, Neetu [1 ]
Sahoo, Monalisa [2 ]
Mallik, Sumanta Kumar [1 ]
Sarma, Debajit [1 ]
Das, Partha [1 ]
机构
[1] Directorate Coldwater Fisheries Res, Naini Tal 263136, Uttarakhand, India
[2] Indian Vet Res Inst, Bareilly 243122, Uttar Pradesh, India
关键词
microcystins; zebrafish; genotoxicity; DNA damage; apoptosis; PROTEIN PHOSPHATASE INHIBITION; BLUE-GREEN-ALGAE; IN-VIVO; CYANOBACTERIAL TOXINS; LR; WATER; TOXICITY; GENOTOXICITY; APOPTOSIS; EXTRACTS;
D O I
10.1080/02772248.2011.646111
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Microcystins (MCYST) are the freshwater cyanobacterial toxins, known to induce hepatocellular carcinoma, necrosis, intrahepatic bleeding, as well as human and livestock mortality. Within hepatocytes, MCYST selectively bind to protein phosphatases 1 and 2A, resulting in severe liver damage. The toxicology of MCYST in mice and rats has been well studied, but little is known regarding genotoxicity in aquatic animals. In this study, the zebrafish, Danio rerio was exposed to crude extract of Microcystis aeruginosa bloom. Liver and heart were examined for MCYST-induced toxicity. Light microscopy at 36 h revealed severe, widespread apoptotic necrosis of the majority of hepatocytes, and cytoskeletal deformation in myocardiocytes. Hepatocytes were dissociated with cell shrinkage and margination of nuclear chromatin. Laddering of genomic DNA from the liver and heart of the exposed fish in an increment of 180-200 bp was consistent with apoptosis. Fluorimetric analysis of DNA unwinding was carried out to determine the DNA strand breakage. After 36 h exposure, the % double-stranded DNA was significantly reduced in hepatocytes and myocardiocytes. In conclusion, the results obtained in this study indicate that, the extract of M. aeruginosa bloom is genotoxic to fish. The DNA damage observed in this study may be attributed to the activation of DNA endonucleases. This model of DNA damage may contribute for identifying novel molecular mechanisms of interest for therapeutic application.
引用
收藏
页码:340 / 349
页数:10
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