神经炎症
发病机制
氧化应激
转基因小鼠
医学
机制(生物学)
早老素
中医药
炎症
药理学
治疗方法
疾病
淀粉样前体蛋白
转基因
神经科学
阿尔茨海默病
免疫学
生物
病理
内科学
基因
生物化学
哲学
替代医学
认识论
作者
Haiting An,Dongfeng Wei,Yanjing Qian,Ning Li,Xiaomin Wang
出处
期刊:PubMed
日期:2018-01-01
卷期号:10 (11): 3857-3875
被引量:10
摘要
The pathogenesis of Alzheimer's disease (AD) involves multiple contributing factors, including amyloid β (Aβ) peptide aggregation, inflammation, oxidative stress, and others. Effective therapeutic drugs for treating AD are urgently needed. SQYZ granules (SQYZ), a Chinese herbal preparation, are mainly composed of the ginsenoside Rg1, astragaloside A and baicalin, and have been widely used to treat dementias for decades in China. In this study, we found the therapeutic effects of SQYZ on the cognitive impairments in an AD mouse model, the β-amyloid precursor protein (APP) and presenilin-1 (PS1) double-transgenic mouse, which co-expresses five familial AD mutations (5XFAD); next, we further explored the underlying mechanism and observed that after SQYZ treatment, the Aβ burden and inflammatory reactions in the brain were significantly attenuated. Through a proteomic approach, we found that SQYZ regulated the expression of 27 proteins, mainly those related to neuroinflammation, stress responses and energy metabolism. These results suggested that SQYZ has the ability to improve the cognitive impairment and ameliorate the neural pathological changes in AD, and the therapeutic mechanism may be related to the modulation of multiple processes related to AD pathogenesis, especially anti-neuroinflammation, promotion of stress recovery and improvement of energy metabolism.
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