Jujuboside A, a neuroprotective agent from semen Ziziphi Spinosae ameliorates behavioral disorders of the dementia mouse model induced by Aβ1-42

被引:76
作者
Liu, Zhi [1 ]
Zhao, Xu [1 ]
Liu, Bing [1 ]
Liu, Ai-jing [1 ]
Li, Huan [1 ]
Mao, Xin [1 ]
Wu, Bo [1 ]
Bi, Kai-shun [2 ]
Jia, Ying [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China
关键词
Alzheimer's disease; Jujuboside A; A beta(1-42); Antioxidant; Anti-inflammation; ALZHEIMERS-DISEASE; COGNITIVE IMPAIRMENT; OXIDATIVE STRESS; INTRACEREBROVENTRICULAR-STREPTOZOTOCIN; SUANZAOREN DECOCTION; MEMORY DEFICITS; RAT MODEL; PERFORMANCE; ACID; NEURODEGENERATION;
D O I
10.1016/j.ejphar.2014.05.041
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Semen Ziziphi Spinosae (SZS) has been used as a hypnotic-sedative medicine for thousands of years. Recently, SZS has also shown notable neuroprotective activities via anti-oxidative and anti-inflammatory effects in dementia animals. Jujuboside A (JuA), isolated from SZS, has been proved to be a major hypnotic-sedative component of SZS. In the present study, we firstly evaluated the effects of intracerebroventricular (ICV) injection of JuA (0.02 and 0.2 mg/kg) for five consecutive days on cognitive impairment induced by ICV injection of A beta(1-42). The results showed that ICV treatment with JuA significantly mitigated learning and memory impairment in mice induced by A beta(1-42) as measured by the Y-maze, active avoidance and Morris water maze. Furthermore, ICV treatment with JuA reduced the level of A beta(1-42) in hippocampus, significantly inhibited the activities of acetylcholinesterase (AChE) and NO, and decreased the amount of the increased malondialdehyde (MDA) in the hippocampus and cerebral cortex of mice treated with ICV injection of A beta(1-42).Shrinkage of nuclei, swollen and eccentrically dispersed neuronal bodies were observed in hippocampus of AD mice induced by A beta(1-42), however, JuA noticeably improved the histopathological damage. Cumulatively, the present study indicates that JuA may serve as a potential therapeutic agent for the treatment of Alzheimer's disease. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:206 / 213
页数:8
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