期刊
FOOD AND CHEMICAL TOXICOLOGY
卷 60, 期 -, 页码 302-308出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2013.07.072
关键词
Dimethyltin (DMT); Dibutyltin (DBT); Diphenyltin (DPT); Neurotoxicity; Apoptosis; PC12 cells
资金
- National Natural Science Foundation of China [81101687]
- Innovative Drug Development State Key Science and Technology of China [2009ZX09103-104]
- Program for the Top Science and Technology Innovation Teams of Higher Learning Institutions of Shanxi Province
- Program for the Top Young and Middle-aged Innovative Talents of Higher Learning Institutions of Shanxi Province
As ubiquitous environmental toxicants, organotin (IV) compounds (OTC) accumulate in the food chain and potential effects on human health are disquieting. The present study compared the cytotoxicity of three diorganotins, namely, dimethyltin (DMT), dibutyltin (DBT) and diphenyltin (DPT), in rat pheochromocytoma (PC12) cells, and the molecular mechanisms responsible for their cytotoxic effects were also explored. Twenty-four hours exposure of PC12 cells to DBT and DPT resulted in a concentration-dependent decrease in cell viability with median lethal concentration (LC50) of 2.97 mu M and 7.24 mu M, respectively. However, DMT at concentrations up to 128 mu M had no obvious effect on cell viability. The mechanistic study revealed that the extent of apoptosis was greater for DBT than that for DPT, followed by DMT, as evidenced by acridine orange/ethidium bromide (AO/EB) fluorescent staining method and annexin V-FITC/PI staining flow cytometry analysis, as well as generation of intracellular reactive oxygen species (ROS), mitochondrial membrane potential (MMP) disruption, release of cytochrome c (Cyt c), and consequent activation of caspase-9, and -3. These investigations suggested that the cytotoxic potency of three diorganotins in PC12 cells was in the order of DBT > DPT >> DMT, and these compounds could induce PC12 cells apoptosis through ROS mediated mitochondrial pathway. (C) 2013 Elsevier Ltd. All rights reserved.
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