Classic Famous Prescription Kai-Xin-San Ameliorates Alzheimer’s Disease via the Wnt/β-Catenin Signaling Pathway

被引:0
|
作者
Xiaoxiao Shan
Shujie Lv
Peng Huang
Wei Zhang
Chuanshan Jin
Yuanxu Liu
Yangyang Li
Yong Jia
Xiaoqin Chu
Can Peng
Caiyun Zhang
机构
[1] Anhui University of Chinese Medicine,Anhui Academy of Chinese Medicine
[2] Anhui Education Department (AUCM),Engineering Technology Research Center of Modernized Pharmaceutics
[3] Institute of Pharmacokinetics,School of Pharmacy
[4] Anhui University of Chinese Medicine,Anhui Province Key Laboratory of Pharmaceutical Preparation Technology and Application
[5] Anhui Genuine Chinese Medicinal Materials Quality Improvement Collaborative Innovation Center,undefined
[6] Anhui University of Chinese Medicine,undefined
来源
Molecular Neurobiology | 2024年 / 61卷
关键词
Classic famous prescription; Kai-Xin-San; TCM; Alzheimer’s disease; Cognitive impairment; Wnt; β-Catenin;
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学科分类号
摘要
Kai-Xin-San (KXS) is a classic famous prescription composed of Polygalae Radix, Ginseng Radix et Rhizoma, Acori Tatarinowii Rhizoma, and Poria. Clinically, KXS is effective in treating amnesia and regulating cognitive dysfunction of Alzheimer’s disease (AD), whereas its mechanism of action is still unclear. In this study, the AD model rats were established by combining intraperitoneal injection of D-galactose (150 mg/kg/day) and intracerebral injection of Aβ25-35 (10 μL) to investigate the meliorative effect of KXS on AD and explore its mechanism. After 1-month KXS treatment, Morris water maze test showed that different doses of KXS all improved the cognitive impairment of AD rats. The results of hematoxylin and eosin staining, Nissl staining, and Tunnel staining showed that the neuron injury in the hippocampal CA1 region of the AD rats was markedly improved after KXS treatment. Concurrently, KXS reversed the levels of biochemical indexes of AD rats. Furthermore, the protein expressions of Wnt1 and β-catenin in KXS groups were remarkably increased, while the expressions of Bax and caspase-3 were significantly decreased. Besides, KXS-medicated serum reduced the levels of tumor necrosis factor-α, interleukin-1β, and reactive oxygen species and regulated the protein expressions of β-catenin, glycogen synthase kinase-3β (GSK-3β), p-GSK-3β, Bax, and caspase-3 in Aβ25-35-induced pheochromocytoma cells. Most importantly, this effect was attenuated by the Wnt inhibitor IWR-1. Our results suggest that KXS improves cognitive and memory function of AD rats, and its neuroprotective mechanism may be mediated through the Wnt/β-catenin signaling pathway.
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页码:2297 / 2312
页数:15
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