Neuroprotective effects of 20(S)-protopanaxatriol (PPT) on scopolamine-induced cognitive deficits in mice

被引:39
|
作者
Lu, Cong [1 ,2 ,3 ]
Lv, Jingwei [1 ,2 ]
Dong, Liming [1 ,2 ]
Jiang, Ning [1 ,2 ]
Wang, Yan [3 ]
Wang, Qiong [4 ]
Li, Yinghui [5 ]
Chen, Shanguang [5 ]
Fan, Bei [3 ]
Wang, Fengzhong [3 ]
Liu, Xinmin [1 ,2 ]
机构
[1] CAMS, Inst Med Plant Dev IMPLAD, Res Ctr Pharmacol & Toxicol, Beijing 100193, Peoples R China
[2] PUMC, Beijing 100193, Peoples R China
[3] CAAS, Inst Food Sci & Technol, Beijing 100193, Peoples R China
[4] Southwest Med Univ, Sinoportugal TCM Int Cooperat Ctr, Affiliated TCM Hosp, Sch Pharm, Luzhou 646000, Peoples R China
[5] China Astronaut Res & Training Ctr, State Key Lab Space Med Fundamentals & Applicat, Natl Lab Human Factors Engn, Beijing 100094, Peoples R China
基金
中国国家自然科学基金;
关键词
20(S)-protopanaxatriol (PPT); cholinergic function; cognitive deficits; oxidative stress; scopolamine; MEMORY IMPAIRMENT; OBJECT-RECOGNITION; ALZHEIMERS-DISEASE; RATS; STRESS; GINSENOSIDES; IMPROVEMENT; EXPRESSION; RECEPTOR; CELLS;
D O I
10.1002/ptr.6044
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
20(S)-protopanaxatriol (PPT), one of the ginsenosides from Panax ginseng, has been reported to have neuroprotective effects and to improve memory. The present study was designed to investigate the protective effect of PPT on scopolamine-induced cognitive deficits in mice. Male Institute of Cancer Research mice were pretreated with 2 different doses of PPT (20 and 40mol/kg) for 27days by intraperitoneal injection, and scopolamine (0.75mg/kg) was injected intraperitoneally for 9days to induce memory impairment. Thirty minutes after the last pretreatment, the locomotor activity was firstly examined to evaluate the motor function of mice. Then, memory-related behaviors were evaluated, and the related mechanism was further researched. It was founded that PPT treatment significantly reversed scopolamine-induced cognitive impairment in the object location recognition experiment, the Morris water maze test, and the passive avoidance task, showing memory-improving effects. PPT also significantly improved cholinergic system reactivity and suppressed oxidative stress, indicated by inhibition of acetylcholinesterase activity, elevation of acetylcholine levels, increasing superoxide dismutase activity and lowering levels of malondialdehyde in the hippocampus. In addition, the expression levels of Egr-1, c-Jun, and cAMP responsive element binding in the hippocampus were significantly elevated by PPT administration. These results suggest that PPT may be a potential drug candidate for the treatment of cognitive deficit in Alzheimer's disease.
引用
收藏
页码:1056 / 1063
页数:8
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