Anhui Academy of Chinese Medicine, Anhui University of Chinese Medicine, Hefei, 230012, People's Republic of China.
Engineering Technology Research Center of Modernized Pharmaceutics, Anhui Education Department (AUCM), Hefei, 230012, Anhui, China.
Mol Neurobiol. 2024 Apr;61(4):2297-2312. doi: 10.1007/s12035-023-03707-y. Epub 2023 Oct 24.
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 Aβ (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 Aβ-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.
开心散(KXS)是由远志、人参、石菖蒲和茯苓组成的经典名方。临床上,KXS 对治疗健忘症和调节阿尔茨海默病(AD)的认知功能障碍有效,但作用机制尚不清楚。在这项研究中,通过腹腔注射 D-半乳糖(150mg/kg/天)和脑内注射 Aβ(10μL)联合建立 AD 模型大鼠,以研究 KXS 对 AD 的改善作用及其机制。经过 1 个月的 KXS 治疗,Morris 水迷宫测试表明,不同剂量的 KXS 均改善了 AD 大鼠的认知障碍。苏木精-伊红染色、尼氏染色和 Tunnel 染色结果表明,KXS 处理后 AD 大鼠海马 CA1 区神经元损伤明显改善。同时,KXS 逆转了 AD 大鼠的生化指标水平。此外,KXS 组的 Wnt1 和β-连环蛋白蛋白表达显著增加,而 Bax 和 caspase-3 表达明显减少。此外,KXS 介导的血清降低了肿瘤坏死因子-α、白细胞介素-1β和活性氧的水平,并调节了 Aβ 诱导的嗜铬细胞瘤细胞中β-连环蛋白、糖原合酶激酶-3β(GSK-3β)、p-GSK-3β、Bax 和 caspase-3 的蛋白表达。最重要的是,Wnt 抑制剂 IWR-1 减弱了这种作用。我们的结果表明,KXS 改善了 AD 大鼠的认知和记忆功能,其神经保护机制可能是通过 Wnt/β-连环蛋白信号通路介导的。