Alzheimer's Center at Temple, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA; Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Viale Ferdinando Stagno D' Alcontres 31. 98166 Messina, Italy.
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Viale Ferdinando Stagno D' Alcontres 31. 98166 Messina, Italy.
Pharmacol Ther. 2022 Oct;238:108178. doi: 10.1016/j.pharmthera.2022.108178. Epub 2022 Mar 26.
Defects in cellular functions related to altered protein homeostasis and associated progressive accumulation of pathological intracellular material is a critical process involved in the pathogenesis of many neurodegenerative disorders, including Alzheimer's disease and Parkinson's disease. Autophagy is an essential mechanism that ensures neuronal health by removing long-lived proteins or defective organelles and by doing so prevents cell toxicity and death within the central nervous system. Abundant evidence has shown that neuronal autophagy pathways are altered in Alzheimer's disease, Parkinson's disease and traumas of the central nervous system including Spinal Cord Injury and Traumatic Brain Injury. In this review, we aimed to summarize the latest studies on the role that altered neuronal autophagy plays in brain health and these pathological conditions, and how this knowledge can be leveraged for the development of novel therapeutics against them.
细胞功能缺陷与蛋白质动态平衡改变有关,而与异常细胞内物质的进行性积累相关,这是许多神经退行性疾病(包括阿尔茨海默病和帕金森病)发病机制中的一个关键过程。自噬是一种重要的机制,通过清除寿命长的蛋白质或有缺陷的细胞器来确保神经元的健康,从而防止中枢神经系统内的细胞毒性和死亡。大量证据表明,阿尔茨海默病、帕金森病以及中枢神经系统损伤(包括脊髓损伤和创伤性脑损伤)中神经元自噬途径发生了改变。在这篇综述中,我们旨在总结最新研究关于改变的神经元自噬在大脑健康和这些病理状况中的作用,以及如何利用这些知识开发针对它们的新型治疗方法。
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