Neuroprotective effect and mechanism of daucosterol palmitate in ameliorating learning and memory impairment in a rat model of Alzheimer's disease

被引:27
|
作者
Ji, Zhi-Hong [1 ]
Xu, Zhong-Qi [1 ]
Zhao, Hong [2 ]
Yu, Xin-Yu [1 ]
机构
[1] Dalian Univ, Coll Med, Neurosci Lab, Dalian 116622, Peoples R China
[2] Dalian Univ, Coll Med, Dept Tradit Chinese Med, Dalian 116622, Peoples R China
关键词
Daucosterol palmitate; Alzheimer's disease; Learning and memory; Reactive oxygen species; Hippocampal neurons; Synaptophysin; HIPPOCAMPAL CA1 NEURONS; OXIDATIVE STRESS; SYNAPTOPHYSIN IMMUNOREACTIVITY; SYNAPTIC PLASTICITY; CORTICAL-NEURONS; A-BETA; GLUTAMATE; PEPTIDE; PROTEIN; BRAIN;
D O I
10.1016/j.steroids.2017.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is an age-related neurodegenerative disorder characterized by progressive memory decline and cognitive impairment. Amyloid beta (A beta) has been proposed as the causative role for the pathogenesis of AD. Accumulating evidence demonstrates that A beta neurotoxicity is mediated by glutamate excitotoxicity. Daucosterol palmitate (DSP), a plant steroid with anti-glutamate excitotoxicity effect, was isolated from the anti-aging traditional Chinese medicinal herb Alpinia oxyphylla Miq. in our previous study. Based on the anti-glutamate excitotoxicity effect of DSP, in this study we investigated potential benefit and mechanism of DSP in ameliorating learning and memory impairment in AD model rats. Results from this study showed that DSP administration effectively ameliorated A beta-induced learning and memory impairment in rats, markedly inhibited A beta-induced hippocampal ROS production, effectively prevented A beta-induced hippocampal neuronal damage and significantly restored hippocampal synaptophysin expression level. This study suggests that DSP may be a potential candidate for development as a therapeutic agent for AD cognitive decline. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:31 / 35
页数:5
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