She Lingyu, Sun Jinfeng, Xiong Li, Li Ankang, Li Liwei, Wu Haibin, Ren Juan, Wang Wei, Liang Guang, Zhao Xia
Department of Pharmacy, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang 310014, China; Key Laboratory of Natural Medicines of the Changbai Mountain, Ministry of Education, Yanbian University, Yanji, Jilin 133002, China.
Key Laboratory of Natural Medicines of the Changbai Mountain, Ministry of Education, Yanbian University, Yanji, Jilin 133002, China.
Phytomedicine. 2024 Jan;122:155168. doi: 10.1016/j.phymed.2023.155168. Epub 2023 Oct 30.
The pathogenesis of Alzheimer's disease (AD) is complex, resulting in unsatisfactory effects of single-target therapeutic drugs. Accumulation evidence suggests that low toxicity multi-target drugs may play effective roles in AD. Ginseng is the root and rhizome of Panax ginseng Meyer, which can be used not only as herbal medicine but also as a functional food to support body functions. Ginsenoside RK1 (RK1), obtained from ginseng plants through high-temperature treatment, has antiapoptotic, antioxidant, anti-inflammatory effects and these events are involved in the development of AD. So, we believe that RK1 may be an effective drug for the treatment of AD.
HYPOTHESIS/PURPOSE: We aimed to investigate the potential protective effects and mechanisms of RK1 in AD.
Neuronal damage was detected by MTT assay, LDH assay, immunofluorescence and western blotting. Oxidative stress was measured by JC-1 staining, reactive oxygen species (ROS) staining, superoxide dismutase (SOD) and malonaldehyde (MDA). The cognitive deficit was measured through morris water maze (MWM) and novel object recognition (NOR) tests.
RK1 attenuated Aβ-induced apoptosis, restored mitochondrial membrane potential (ΔΨm), and reduced intracellular levels of ROS in both PC12 cells and primary cultured neurons. In vivo, RK1 significantly improved cognitive deficits and mitigated AD-like pathological features. Notably, RK1 demonstrated superior efficacy compared to the positive control drug, donepezil. Mechanistically, our study elucidates that RK1 modulates the phosphorylation of AMP-activated protein kinase (AMPK) and its downstream target, NF-E2-related factor 2 (Nrf2), leading to the optimization of mitochondrial membrane potential, reduction of ROS levels, and mitigation of AD-like pathology. It's noteworthy that blocking the AMPK signaling pathway attenuated the protective effects of RK1.
RK1 demonstrates superior efficacy in alleviating cognitive deficits and mitigating pathological changes compared to donepezil. These findings suggest the potential utility of RK1-based therapies in the development of treatments for AD.
阿尔茨海默病(AD)的发病机制复杂,导致单靶点治疗药物的效果不尽人意。越来越多的证据表明,低毒性的多靶点药物可能在AD治疗中发挥有效作用。人参是五加科人参属植物人参的根及根茎,不仅可作为草药,还可作为维持身体机能的功能性食品。通过高温处理从人参植物中获得的人参皂苷RK1(RK1)具有抗凋亡、抗氧化、抗炎作用,而这些作用均与AD的发展有关。因此,我们认为RK1可能是一种治疗AD的有效药物。
假设/目的:我们旨在研究RK1对AD的潜在保护作用及其机制。
通过MTT法、乳酸脱氢酶(LDH)检测法、免疫荧光法和蛋白质免疫印迹法检测神经元损伤。通过JC-1染色、活性氧(ROS)染色、超氧化物歧化酶(SOD)和丙二醛(MDA)检测氧化应激。通过莫里斯水迷宫(MWM)和新物体识别(NOR)试验检测认知缺陷。
RK1可减轻Aβ诱导的细胞凋亡,恢复线粒体膜电位(ΔΨm),并降低PC12细胞和原代培养神经元内的ROS水平。在体内,RK1显著改善认知缺陷并减轻AD样病理特征。值得注意的是,与阳性对照药物多奈哌齐相比,RK1显示出更好的疗效。从机制上讲,我们的研究表明RK1调节腺苷酸活化蛋白激酶(AMPK)及其下游靶点核因子E2相关因子2(Nrf2)的磷酸化,从而优化线粒体膜电位,降低ROS水平,并减轻AD样病理变化。值得注意的是,阻断AMPK信号通路会减弱RK1的保护作用。
与多奈哌齐相比,RK1在减轻认知缺陷和病理变化方面显示出更好的疗效。这些发现表明基于RK1的疗法在AD治疗开发中的潜在效用。