Exploring the Effect of Ginsenoside Rh1 in a Sleep Deprivation-Induced Mouse Memory Impairment Model

被引:42
|
作者
Lu, Cong [1 ,2 ]
Shi, Zhe [3 ]
Dong, Liming [1 ,2 ]
Lv, Jingwei [1 ,2 ]
Xu, Pan [1 ,2 ]
Li, Yinghui [4 ]
Qu, Lina [4 ]
Liu, Xinmin [1 ,2 ,4 ]
机构
[1] Chinese Acad Med Sci, Inst Med Plant Dev IMPLAD, Res Ctr Pharmacol & Toxicol, Beijing, Peoples R China
[2] Peking Union Med Coll, Beijing, Peoples R China
[3] Hunan Univ Chinese Med, Changsha, Hunan, Peoples R China
[4] China Astronaut Res & Training Ctr, Natl Lab Human Factors Engn, State Key Lab Space Med Fundamentals & Applicat, Beijing, Peoples R China
关键词
ginsenoside Rh1; sleep deprivation (SD); cognitive impairment; cortexhippocampus; oxidative stress; ACUTE NICOTINE TREATMENT; LONG-TERM POTENTIATION; OXIDATIVE STRESS; RAT HIPPOCAMPUS; VITAMIN-E; COGNITION; BRAIN; MODAFINIL; MICE;
D O I
10.1002/ptr.5797
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Panax ginseng C.A. Meyer (Araliaceae) has been used in traditional Chinese medicine for enhancing cognition for thousands of years. Ginsenoside Rh1, a constituent of ginseng root, as with other constituents, has memory-improving effects in normal mice and scopolamine-induced amnesic mice. Sleep deprivation (SD) is associated with memory impairment through induction of oxidative stress. The present study investigated the effect of Rh1 against SD-induced cognitive impairment and attempted to define the possible mechanisms involved. Ginsenoside Rh1 (20mol/kg; 40mol/kg) and modafinil (0.42g/kg) were administered to the mice intraperitoneally for 23days. After 14-day SD, locomotor activity was examined using the open field test, and the object location recognition and Morris water maze tests were used to evaluate cognitive ability. The cortex and hippocampus were then dissected and homogenized, and levels and activities of antioxidant defense biomarkers were evaluated to determine the level of oxidative stress. The results revealed that Rh1 prevented cognitive impairment induced by SD, and its ability to reduce oxidative stress in cortex and hippocampus may contribute to the mechanism of action. Copyright (c) 2017 John Wiley & Sons, Ltd.
引用
收藏
页码:763 / 770
页数:8
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