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KMID : 0617220020130010157
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Duksung Bulletin Phamaceutical Sciences
2002 Volume.13 No. 1 p.157 ~ p.163
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2,3,7,8-Tetrachlorobenzo-ρ-dioxin Inhibits Proliferation of SK-N-SH Human Neuronal Cells Through Decreased Production of Reactive Oxygen Species
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LEE, YONG SOO
JIN, DA-QING/PARK, SEUNG HEE/HAN, SOON YOUNG/KIM, HYUNG SIK/JEONG, TAE CHEON/HUH, KEUN
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Abstract
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Oxidative stress has been known to be involved in the mechanism of toxic effects of various agents on many cellular systems. In this study we investigated the role of reactive oxygen species (ROS) in 2,3,7,8-tetrachloro-dibenzo-p-dioxin (TCDD)-induced neuronal cell toxicity using SK-N-SH human neuroblastoma cells. TCDD inhibited proliveration of the cells in a dose-dependent manner, which was revealed by MTT staining, counting of cells stained with trypan blue and [^3H]thymidine uptake assay. TCDD also suppressed the basal generation of ROS in a time-and concentration-dependent manner assessed by 2′,7′-dichlorofluorescein fluorescence. In addition, TCDD induced a dose-dependent inhibition of lipid peroxidation, a biomarker of oxidative stress, whereas it significantly increased the level of glutathione (GSH), an intracellular free radical scavenger in the cells. Moreover, TCDD altered the activities of major antioxidant enzymesw; increase in superoxide dismutase (SOD) and catalase, but decrease in glutathione peroxidase (GSH-Px) and glutathione reductase (GSH-Red). Pretreatment with L-buthionine-S, R-sulfoximine (BSO, 50uM), an ingibitor of GSH synthesis, significantly prevented the TCDD-induced reduction in lipid peroxidation and cell proliferation. Interestingly, exogenous application of an oxidant, H_2O_2(50㎛) markedly restored the inhibited cell proliferation induced by TCDD. Taken together, these results suggest that alteration of cellular redox balance may mediate the TCDD-induced inhibition of proliferation in human neuronal cells.
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