Article ID Journal Published Year Pages File Type
5862572 Toxicology in Vitro 2011 9 Pages PDF
Abstract
► An increase ROS level with a decrease in glutathione level suggests nano-SiO2-induced free radical generation and glutathione depletion. ► A decrease in cell viability associated with ROS level suggests the role of oxidative stress on nano-SiO2 induced cell death. ► An increase in thiobarbituric-acid reactive species level suggests nano-SiO2-induced membrane damage caused by lipid peroxidation. ► An increase in a cell shrinkage and a nuclear condensation suggesting nano-SiO2-induced cell apoptosis. ► Nano-SiO2 exposure diminishes the ability of neurite extension in response to NGF in treated PC12 cells.
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