Epigallocatechin-3-gallate Alleviates Cognitive Deficits in APP/PS1 Mice

被引:0
|
作者
Jian Bao
Wei Liu
Hong-yan Zhou
Yu-ran Gui
You-hua Yang
Meng-juan Wu
Yi-fan Xiao
Jin-ting Shang
Gui-feng Long
Xi-ji Shu
机构
[1] Jianghan University,Department of Pathology and Pathophysiology, School of Medicine
[2] Jianghan University,Department of Traditional Chinese Medicine, School of Medicine
[3] Jianghan University,Department of Physiology, School of Medicine
[4] Jianghan University,Institutes of Biomedical Sciences, School of Medicine
[5] Jianghan University,School of Life Science
来源
Current Medical Science | 2020年 / 40卷
关键词
Alzheimer’s disease; cognitive impairments; epigallocatechin-3-gallate; anti-inflammation; β-amyloid;
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中图分类号
学科分类号
摘要
Alzheimer’s disease (AD) shows cognitive impairments in clinic, which is multifactorial with different etiopathogenic mechanisms such as Aβ deposition, neuroinflammation and neuronal dystrophy involved. Therefore, multi-targets drugs with neuroprotective, anti-amyloidogenic and anti-inflammatory properties will be effective in AD treatment. Epigallocatechin-3-gallate (EGCG) possesses a broad spectrum of pharmacological activities in the prevention and treatment of multiple neurodegenerative diseases. In the present study, we showed that oral administration of EGCG (50 mg/kg) for 4 months significantly attenuated the cognitive deficits in APP/PS1 transgenic mice, which served as AD model. Moreover, EGCG induced an improvement in dendritic integrity and expression levels of synaptic proteins in the brain of APP/PS1 mice. And EGCG exerted obvious anti-inflammatory effects, which was manifested by alleviating microglia activation, decreasing pro-inflammatory cytokine (IL-1β) and increasing anti-inflammatory cytokines (IL-10, IL-13). Furthermore, β-amyloid (Aβ) plaques were markedly reduced in the hippocampus of 6-month old APP/PS1 mice after EGCG treatment. In conclusion, these findings indicate that EGCG improves AD-like cognitive impairments through neuroprotective, anti-amyloidogenic and anti-inflammatory effects, thus is a promising therapeutic candidate for AD.
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页码:18 / 27
页数:9
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