Kopeć Kamila, Koziorowski Dariusz, Szlufik Stanisław
Department of Neurology, Faculty of Health Sciences, Medical University of Warsaw, Żwirki i Wigury 61, 02-091 Warsaw, Poland.
Int J Mol Sci. 2025 Aug 5;26(15):7552. doi: 10.3390/ijms26157552.
Neurodegenerative disorders, including Alzheimer's disease (AD), are a growing problem in aging society. The amyloid cascade hypothesis has recently been questioned, and therapies based on it have not yielded the expected results. However, the role of amyloid-β (Aβ) in AD pathogenesis cannot be rejected. It appears that some of the key players in the pathogenesis of the disease are the soluble amyloid-β oligomers. Soluble amyloid-β oligomers have neurotoxic effects by disrupting intracellular Ca homeostasis and impairing mitochondrial function. The glymphatic system is an important pathway for the removal of soluble amyloid forms from the brain. The decline in the activity of this system is observed in aging brains, which is correlated with the occurrence of Alzheimer's disease, primarily among the elderly population. Therefore, the question arises as to whether the glymphatic system could be another potential target for therapeutic interventions in Alzheimer's disease. In this regard, it is imperative to pay attention to the factors that contribute to the pathogenesis of Alzheimer's disease and also impact the glymphatic system, such as sleep, physical activity, alcohol consumption, and supplementation with polyunsaturated fatty acids. The question remains whether the glymphatic system will become the key to treating Alzheimer's disease.
包括阿尔茨海默病(AD)在内的神经退行性疾病,在老龄化社会中是一个日益严重的问题。淀粉样蛋白级联假说最近受到质疑,基于该假说的治疗方法并未产生预期效果。然而,β-淀粉样蛋白(Aβ)在AD发病机制中的作用不能被否定。看来,该疾病发病机制中的一些关键因素是可溶性淀粉样β寡聚体。可溶性淀粉样β寡聚体通过破坏细胞内钙稳态和损害线粒体功能而具有神经毒性作用。类淋巴系统是从大脑中清除可溶性淀粉样蛋白形式的重要途径。在衰老的大脑中观察到该系统的活性下降,这与阿尔茨海默病的发生相关,主要发生在老年人群中。因此,问题在于类淋巴系统是否可能成为阿尔茨海默病治疗干预的另一个潜在靶点。在这方面,必须关注导致阿尔茨海默病发病机制并影响类淋巴系统的因素,如睡眠、体育活动、饮酒以及补充多不饱和脂肪酸。类淋巴系统是否会成为治疗阿尔茨海默病的关键,这一问题仍然存在。