期刊
TOXICOLOGY
卷 261, 期 3, 页码 119-125出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.tox.2009.05.002
关键词
Synthetic pyrethroids; Bifenthrin; Enantioselectivity; Apoptosis; MAPKs
资金
- National Natural Science Foundations of China [20837002]
- Natural Science Foundation of Zhejiang Province, China [Z506070]
- National Basic Research Program of China [2009CB421603]
- Program for Changjiang Scholars and Innovative Research Team in Chinese Universities [IRT 0653]
Enantioselectivity in toxicology, and health risk of chiral xenobiotics have become important topics at the forefront of chemistry and toxicology research. Our previous results showed that cis-bifenthrin (cis-BF) induced cytotoxicity and genotoxicity in human amnion epithelial (FL) cells, in an enantioselective manner. However, the exact molecular mechanisms of synthetic pyrethroid-induced, enantioselective apoptosis and cytotoxicity remain unclear. In this study, enantiomers of the synthetic pyrethroid-based insecticide, cis-BF, were separated on selected chiral columns by HPLC. Enantioselectivity in cytotoxicity and apoptosis, mediated by the mitogen-activated protein kinase (MAPK) signalling pathway, were evaluated in the human hepatocellular liver carcinoma (Hep G2) cell line. Exposure to 1S-cis-BF resulted in increased levels of phosphorylated JNK (Jun-N-terminal Kinases)/MAPKs, while exposure to 1R-cis-BF did not affect phosphorylated JNK levels. Pre-treatment with the JNK inhibitor SP600125, blocked 1S-cis-BF-induced cytotoxicity and apoptosis. In addition, 1S-cis-BF enhanced the production of ROS, while pre-treatment with the antioxidant agent MnTBAP resulted in decreased phosphorylation of JNK. To the best of our knowledge, this is the first report demonstrating that cis-BF-induced apoptosis might occur, at least in part, through the enantioselective activation of JNK/MAPK signalling pathway in Hep G2 cells. The results suggest that enantioselectivity should be considered when evaluating eco-toxicological effects and health risks of chiral contaminants, and could also improve the understanding of molecular mechanisms responsible for chiral chemical-induced cytotoxicity and apoptosis. (c) 2009 Elsevier Ireland Ltd. All rights reserved.
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