Long-term Ginsenoside Rg1 Supplementation Improves Age-Related Cognitive Decline by Promoting Synaptic Plasticity Associated Protein Expression in C57BL/6J Mice

被引:46
作者
Yang, Lumeng [1 ]
Zhang, Jing [1 ]
Zheng, Kunmu [2 ]
Shen, Hui [1 ]
Chen, Xiaochun [1 ,3 ,4 ]
机构
[1] Fujian Med Univ, Affiliated Union Hosp, Fujian Inst Geriatr, Key Lab Brain Aging & Neurodegenerat Dis, Fuzhou 350001, Fujian, Peoples R China
[2] Xiamen Univ, Affiliated Hosp 1, Xiamen, Peoples R China
[3] Fujian Med Univ, Union Hosp, Dept Neurol, Fuzhou 350001, Fujian, Peoples R China
[4] Fujian Med Univ, Ctr Neurobiol, Fuzhou 350001, Fujian, Peoples R China
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2014年 / 69卷 / 03期
关键词
Aging; Ginsenoside; Cognition; Synapse; mTOR; RECOGNITION MEMORY CONSOLIDATION; MAMMALIAN TARGET; RAPAMYCIN MTOR; AMYLOID-BETA; KINASE-II; TRANSLATIONAL CONTROL; FEAR MEMORY; MOUSE MODEL; LIFE-SPAN; INHIBITION;
D O I
10.1093/gerona/glt091
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
In aging individuals, age-related cognitive decline is the most common cause of memory impairment. Among the remedies, ginsenoside Rg1, a major active component of ginseng, is often recommended for its antiaging effects. However, its role in improving cognitive decline during normal aging remains unknown and its molecular mechanism partially understood. This study employed a scheme of Rg1 supplementation for female C57BL/6J mice, which started at the age of 12 months and ended at 24 months, to investigate the effects of Rg1 supplementation on the cognitive performance. We found that Rg1 supplementation improved the performance of aged mice in behavior test and significantly upregulated the expression of synaptic plasticity-associated proteins in hippocampus, including synaptophysin, N-methyl-D-aspartate receptor subunit 1, postsynaptic density-95, and calcium/calmodulin-dependent protein kinase II alpha, via promoting mammalian target of rapamycin pathway activation. These data provide further support for Rg1 treatment of cognitive degeneration during aging.
引用
收藏
页码:282 / 294
页数:13
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