Salidroside ameliorates cognitive impairment in a D-galactose-induced rat model of Alzheimer's disease

被引:139
|
作者
Gao, Jin [1 ]
He, He [1 ]
Jiang, Wenjiao [2 ]
Chang, Xiayun [1 ]
Zhu, Lingpeng [1 ]
Luo, Fen [1 ]
Zhou, Rui [1 ]
Ma, Chunhua [1 ]
Yan, Tianhua [1 ]
机构
[1] China Pharmaceut Univ, Dept Physiol & Pharmacol, Nanjing, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Sch Pharm, Nanjing, Jiangsu, Peoples R China
关键词
Sal; Cognitive impairment; Anti-inflammation; Anti-apoptosis; THIOREDOXIN-INTERACTING PROTEIN; OXIDATIVE STRESS; INFLAMMATION; CELLS; ACTIVATION; APOPTOSIS; PATHWAY; MICE;
D O I
10.1016/j.bbr.2015.06.045
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The purpose of the present study was to investigate possible preventive effects of salidroside (sal) on a rat model of Alzheimer's disease and to explore its possible mechanism. Sub-acute aging was induced in male SD rats by subcutaneous injection of D-gal (120 mg/kg) for 42 days, and the rats were treated with sal (20, 40 mg/kg) or normal saline for 28 days after 14 days of D-gal injection. Morris water maze (MWM) test and step-down passive avoidance test were conducted to evaluate the cognitive function of the rats. The levels of inflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and interleukin-1 beta (IL-1 beta) in hippocampus were assayed by enzyme-linked immunosorbent assay (ELISA) to assess the anti-inflammatory effect of sal. Further, we estimated the expression levels of thioredoxin (Trx), thioredoxin interacting protein (Txnip/vitamin D3 up-regulated protein/thioredoxin binding protein-2), Bax, Bcl-2, caspase-9 and related-proteins of nuclear factor kappa B (NF-kappa B) signaling pathway by western blot assay. It showed that administration of sal significantly attenuated all the D-gal-induced changes in the hippocampus, including cognitive impairment and neuroinflammation. These analytical results provides evidence that sal can improve cognitive capacity by inhibiting neuroinflammation and affecting apoptosis-related proteins in hippocampus. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 33
页数:7
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