Differential effects of diallyl disulfide on neuronal cells depend on its concentration

被引:20
作者
Kim, JG
Koh, SH
Lee, YJ
Lee, KY
Kim, Y
Kim, S
Lee, MK
Kim, SH
机构
[1] Chungbuk Natl Univ, Coll Pharm, Dept Pharm, Cheongju, Chungbuk, South Korea
[2] KFDA, Natl Inst Toxicol Res, Dept Toxicol Res, Seoul, South Korea
[3] Hanyang Univ, Coll Med, Dept Neurol, Seoul 133791, South Korea
关键词
diallyl disulfide; antioxidant; apoptosis; PI3K; Akt;
D O I
10.1016/j.tox.2005.02.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diallyl disulfide (DADS) is one of the organosulfur compounds of garlic. The effects of DADS on neuronal cells have not clearly been established. We investigated its effects on the viability of neuronal cells (NI 8D3 cells), the levels of free radical and membrane lipid peroxidation, and the cell signals, such as phosphatidylinositol 3-kinase (PI3K)/Akt and glycogen synthase kinase-3 (GSK-3). When N18D3 cells were treated with several concentrations of DADS, the viability was not affected up to 25 mu M, however, decreased at higher than 25 mu M. The levels of free radicals and membrane lipid peroxidation were increased in a dose-dependent manner, especially at higher than 25 mu M, The treatment of N 18133 cells with 25 mu M DADS slightly increased the expressions of p85a PI3K, phosphorylated Akt and phosphorylated GSK-3, but the treatment with 100 mu M significantly reduced them. To evaluate whether low concentration of DADS, up to 25 mu M, had protective effect on oxidative stress-injured N I 8D3 cells, the viability of N I 8D3 cells (pretreated with DADS for 2 h versus not pretreated) was evaluated 24 h after their exposure to 100 mu M H2O2 for 30 min. Compared to the cells treated with only 100 mu M H2O2, the pretreatment with 25 mu M DADS increased the viability, and the expressions of p85a PI3K, phosphorylated Akt and phosphorylated GSK-3. These results indicate that low concentration of DADS has protective effects on N18D3 cells, whereas high concentration is rather cytotoxic. Therefore, some specific optimum concentration of DADS may be a new potential therapeutic strategy for oxidative stress-injury in vitro model of neurodegenerative diseases. (c) 2005 Published by Elsevier Ireland Ltd.
引用
收藏
页码:86 / 96
页数:11
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