Neuroprotective Properties of Panax notoginseng Saponins via Preventing Oxidative Stress Injury in SAMP8 Mice

被引:36
|
作者
Huang, Jin-Lan [1 ,2 ]
Jing, Xin [3 ]
Tian, Xin [4 ]
Qin, Mei-Chun [5 ]
Xu, Zhe-Hao [5 ]
Wu, Deng-Pan [1 ,2 ]
Zhong, Zhen-Guo [5 ]
机构
[1] Xuzhou Med Univ, Sch Pharm, Jiangsu Key Lab New Drug Res & Clin Pharm, Xuzhou 221004, Jiangsu, Peoples R China
[2] Xuzhou Med Univ, Sch Pharm, Dept Pharmacol, Xuzhou 221004, Jiangsu, Peoples R China
[3] Xian Med Coll, Dept Pharmacol, Xian 710309, Shangxi, Peoples R China
[4] Guangxi Adverse Drug React Monitoring Ctr, Nanning 530029, Guangxi, Peoples R China
[5] Guangxi Univ Chinese Med, Dept Sci & Technol, Nanning 530200, Guangxi, Peoples R China
关键词
UNCOUPLING PROTEINS; DAMAGE; MOUSE; MODEL; BETA;
D O I
10.1155/2017/8713561
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Inhibiting oxidative damage in early stage of Alzheimer's disease (AD) is considered as a strategy for AD treatment. Our previous study has shown that Panax notoginseng saponins (PNS) have an antiaging action by increasing the levels of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-PX) in the serum of aged rats. In this study, we aimed to investigate the effects of PNS on antioxidant enzymes and uncoupling proteins (UCPs) involved in oxidative stress in AD mice. The results showed that PNS prevented neuronal loss in hippocampal CA1 region and alleviated pathomorphological change of neurons in CA1 region. Moreover, PNS inhibited the production of 8-hydroxydeoxyguanosine (8-OHdG), enhanced the expressions and activities of SOD, CAT, and GSH-PX, and improved the mRNA and protein levels of UCP4 and UCP5 in the brains of SAMP8 mice. Together, our study shows that PNS has the ability to protect neurons in AD brain from oxidative stress damage through attenuating the production of 8-OHdG, enhancing the activities of antioxidant enzymes and the expressions levels of UCP4 andUCP5. Accordingly, PNS may be a promising agent for AD treatment.
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页数:7
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