Timosaponin B-II ameliorates scopolamine-induced cognition deficits by attenuating acetylcholinesterase activity and brain oxidative damage in mice

被引:45
|
作者
Zhao, Xu [1 ]
Liu, Chunmei [2 ]
Qi, Yu [2 ]
Fang, Lina [3 ]
Luo, Jie [2 ]
Bi, Kaishun [4 ]
Jia, Ying [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Funct Food & Wine, Wenhua Rd 103, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Wenhua Rd 103, Shenyang 110016, Peoples R China
[3] Shenyang Med Coll, Sch Basic Med Sci, Huanghe North St 146, Shenyang 110034, Peoples R China
[4] Shenyang Pharmaceut Univ, Sch Pharm, Wenhua Rd 103, Shenyang 110016, Peoples R China
基金
中国国家自然科学基金;
关键词
Timosaponin B-II; Alzheimer's disease; Learning and memory; Acetylcholinesterase; Oxidative stress; INDUCED MEMORY IMPAIRMENT; ALZHEIMERS-DISEASE; INDUCED AMNESIA; HUPERZINE; ASPHODELOIDES; SAPONINS; RHIZOMA; STRESS; RADIX;
D O I
10.1007/s11011-016-9877-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Timosaponin B-II (TB-II) is a main active saponin isolated from the rhizome of Anemarrhena asphodeloides Bge., which is widely used in traditional Chinese medicine. In this study, the effect of TB-II on learning and memory was investigated in a scopolamine-induced mouse model of Alzheimer's disease. The results of behavioral tests indicated that TB-II significantly increased the spontaneous alternation in the Y-maze test, and reversed the shortening of step-through latency induced by scopolamine in the passive avoidance test, showing protective effects on short-term and working memory. In the Morris water maze test, TB-II reduced the escape latency time in the training trial, and increased the swimming time in the target quadrant in the probe trial. Biochemical data demonstrated that TB-II significantly inhibited acetylcholinesterase (AChE) activity in the cerebral cortex and hippocampus of mice. Moreover, TB-II markably attenuated the reduction in glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) activities, and decreased malondialdehyde (MDA) levels, which are key biomarkers of brain oxidative stress. These results indicated that TB-II offers protection against scopolamine-induced deficits in learning and memory, possibly by inhibiting AChE and preventing oxidative stress damage. The findings suggested that TB-II has a potential therapeutic effect on cognitive and behavioral impairment.
引用
收藏
页码:1455 / 1461
页数:7
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