维普中文期刊产品整合服务

Kai Xin San ameliorates scopolamine-induced cognitive dysfunction

查看全文 作  者:Yu-Min [1,2]Xu;Xin-Chen [3]Wang;Ting-Ting [1]Xu;Hong-Ying [1]Li;Shang-Yan [1]Hei;Na-Chuan [1]Luo;Hong [1]Wang;Wei [1]Zhao;Shu-Huan [1]Fang;Yun-Bo [1]Chen;Li [1]Guan;Yong-Qi [4]Fang;Shi-Jie [1,5]Zhang;Qi [1,6]Wang;Wei-Xiong [1,6]Liang 高影响力作者 机构地区:[1]Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine;[2]First Affiliated Hospital of Henan University of Chinese Medicine;[3]School of Food and Pharmaceutical Engineering, Zhaoqing University;[4]First Affiliated Hospital of Guangzhou University of Chinese Medicine;[5]Department of Neurology, The First Affiliated Hospital, Guangzhou Medical University;[6]Guangdong Provincial Hospital of Chinese Medicine高影响力机构 出  处:《Neural Regeneration Research》索引2019年第14卷第5期,共11页高影响力期刊 基  金:supported by the National Natural Science Foundation of China,No.81473740,81673627,81673717(to QW);Guangzhou Science Technology and Innovation Commission Technology Research Projects,China,No.2018050100(to QW);the Foundation for Characteristic Innovation of Educational Commission of Guangdong Province,China,Grant No.2016KTSCX011(to SHF);the Open Tending Project for Construction of High-Level University,Guangzhou University of Chinese Medicine,China,No.34 and 118,2017(to SHF);the Technology Platform of Clinical Trials on New Traditional Medicine,China,No.2012ZX09303009-003(to WXL);the Technology Platform of Clinical Evaluation on New Traditional Medicine,China,No.2008ZX09312-021(to WXL) 摘  要:Kai Xin San(KXS, containing ginseng, hoelen, polygala, and acorus), a traditional Chinese herbal compound, has been found to regulate cognitive dysfunction; however, its mechanism of action is still unclear. In this study, 72 specific-pathogen-free male Kunming mice aged 8 weeks were randomly divided into a vehicle control group, scopolamine group, low-dose KXS group, moderate-dose KXS group, high-dose KXS group, and positive control group. Except for the vehicle control group and scopolamine groups(which received physiological saline), the doses of KXS(0.7, 1.4 and 2.8 g/kg per day) and donepezil(3 mg/kg per day) were gastrointestinally administered once daily for 2 weeks. On day 8 after intragastric treatment, the behavioral tests were carried out. Scopolamine group and intervention groups received scopolamine 3 mg/kg per day through intraperitoneal injection. The effects of KXS on spatial learning and memory, pathological changes of brain tissue, expression of apoptosis factors, oxidative stress injury factors, synapse-associated protein, and cholinergic neurotransmitter were measured. The results confirmed the following.(1) KXS shortened the escape latency and increased residence time in the target quadrant and the number of platform crossings in the Morris water maze.(2) KXS increased the percentage of alternations between the labyrinth arms in the mice of KXS groups in the Y-maze.(3) Nissl and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling staining revealed that KXS promoted the production of Nissl bodies and inhibited the formation of apoptotic bodies.(4) Western blot assay showed that KXS up-regulated the expression of anti-apoptotic protein Bcl-2 and inhibited the expression of pro-apoptotic protein Bax. KXS up-regulated the expression of postsynaptic density 95, synaptophysin, and brain-derived neurotrophic factor in the cerebral cortex and hippocampus.(5) KXS increased the level and activity of choline acetyltransferase, acetylcholine, superoxide dismutase, and glutathione peroxidase, and reduced the level and activity of acetyl cholinesterase, reactive oxygen species, and malondialdehyde through acting on the cholinergic system and reducing oxidative stress damage. These results indicate that KXS plays a neuroprotective role and improves cognitive function through reducing apoptosis and oxidative stress, and regulating synapse-associated protein and cholinergic neurotransmitters. 关 键 词:Kai Xin SAN cognitive DYSFUNCTION SCOPOLAMINE hydrobromide neuroprotection oxidative stress SYNAPTIC DYSFUNCTION apoptosis CHOLINERGIC system DYSFUNCTION DONEPEZIL neural regeneration
相关文献

参考文献(66)

引证文献(14)

耦合文献(88)

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费