Neuroprotective effects of polygalacic acid on scopolamine-induced memory deficits in mice

被引:56
作者
Guo, Changrun [1 ]
Shen, Jinyang [1 ]
Meng, Zhaoqing [2 ]
Yang, Xiaolin [3 ]
Li, Fei [1 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
[2] Jiangsu Kanion Pharmaceut Co Ltd, Lianyungang 222001, Peoples R China
[3] Nanjing Univ Chinese Med, Coll Pharm, Jiangsu Key Lab Res & Dev Marine Bioresource Phar, Nanjing 210023, Jiangsu, Peoples R China
关键词
Polygalacic acid; Scopolamine; Memory deficits; Acetylcholine; Neuroinflammation; Oxidative stress; ALZHEIMERS-DISEASE; CHOLINESTERASE-INHIBITORS; COGNITIVE DEFICITS; ACETYLCHOLINE; DEMENTIA; NEUROINFLAMMATION; IMPAIRMENTS; MODELS; RADIX; RATS;
D O I
10.1016/j.phymed.2015.12.009
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Polygala tenuifolia Willd is a Traditional Chinese Medicine used for the treatment of learning and memory deficits. Triterpenoid saponins, the main bioactive compounds of Polygala tenuifolia Willd, are easily hydrolyzed to polygalacic acid (PA). Purpose: The present study was undertaken to investigate the neuroprotective effects of PA on scopolamine-induced cognitive dysfunction and to elucidate its underlying mechanisms of action. Methods: PA (3, 6, and 12 mg/kg) was administered orally to mice for fourteen days, and scopolamine (1 mg/kg) was injected intraperitoneally for fourteen days to induce memory impairment. Memory related behaviors were evaluated using the Morris water maze. Cholinergic and neuroinflammatory activities were measured in brain tissue. Superoxide dismutase activities, malondialdehyde and reduced glutathione contents were also measured in the brains. Results: Treatment with scopolamine significantly increased the escape latency time, decreased the number of crossings, and shortened the time spent in the target quadrant, while PA reversed these scopolamine-induced effects. PA significantly improved cholinergic system reactivity, as indicated by decreased acetylcholinesterase (AChE) activity, increased choline acetyltransferase (ChAT) activity, and elevated levels of acetylcholine (ACh) in the hippocainpus and frontal cortex. PA also significantly ameliorated neuroinflammation and oxidative stress in mice. Conclusion: These results suggest that PA might exert a significant neuroprotective effect on cognitive impairment, driven in part by the modulation of cholinergic activity and neuroinflammation. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:149 / 155
页数:7
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