Protective effect of 3H-1, 2-dithiole-3-thione on cellular model of Alzheimer's disease involves Nrf2/ARE signaling pathway

被引:30
|
作者
Wang, Lan [1 ]
Wang, Min [1 ,2 ]
Hu, Jing [3 ]
Shen, Wei [1 ]
Hu, Junjie [2 ]
Yao, Yi [2 ]
Wang, Xifeng [1 ]
Afzal, Curimbacus M. [2 ]
Ma, Rong [4 ]
Li, Gang [2 ]
机构
[1] Huazhong Univ Sci & Technol, Dept Neurol, Puai Hosp, Tongji Med Coll, Wuhan 430033, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Neurol, Wuhan 430022, Peoples R China
[3] Henan Univ, Huaihe Hosp, Dept Neurol, Kaifeng 47500, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Pharmacol, Wuhan 430030, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; 3H-1; 2-dithiole-3-thione; N2a/APPswe; Nrf2; TRANSCRIPTION FACTOR NRF2; AMYLOID-BETA PEPTIDE; OXIDATIVE STRESS; THERAPEUTIC TARGET; A-BETA; INHIBITION; INDUCTION; DAMAGE; CELLS; ACID;
D O I
10.1016/j.ejphar.2016.12.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nuclear factor erythroid 2-related factor 2 (Nrf2) is a major regulator for a battery of genes encoding detoxifying and antioxidative enzymes. 3H-1, 2-dithiole-3-thione (D3T), a potent free radical scavenger, is able to activate Nrf2 signaling pathway. In the present study, N2a/APPswe cells were used as the Alzheimer's disease (AD) cellular model and we investigated the protective effect of D3T on N2a/APPswe cells and the potential mechanisms. Our assays demonstrated that D3T was able to attenuate reactive oxygen species generation, increase MMP level as well as decrease MDA content. Furthermore, treatment of the cells with 40 mu M D3T for 24 h, showed significant suppression of A beta level in N2a/APPswe cells. The current study also found that D3T significantly upregulated the Nrf2 mRNA level and protein expression, and subsequently enhanced mRNA expression of HO-1 and NQO1 in N2a/APPswe cells. Meanwhile, down-regulation of Nrf2 by small interference RNA abolished cytoprotection of D3T. Taken together, these results demonstrate that D3T provides neuroprotection in vitro model and therefore may be a potential complement for AD therapy.
引用
收藏
页码:115 / 123
页数:9
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