药物发现
化学
粒体自噬
动作(物理)
药物作用
药品
计算生物学
神经科学
药理学
自噬
生物化学
医学
生物
细胞凋亡
物理
量子力学
作者
Panpan Yang,Shuai Wen,Xin Wang,Xiuying Hu,Min Zhao,Aoxue Wang,Yongya Wu,Liang Ouyang,Guan Wang
标识
DOI:10.1021/acs.jmedchem.4c01779
摘要
Neurodegenerative diseases (NDDs), such as Parkinson's disease (PD) and Alzheimer's disease (AD), are devastating brain diseases and are incurable at the moment. Increasing evidence indicates that NDDs are associated with mitochondrial dysfunction. Mitophagy removes defective or redundant mitochondria to maintain cell homeostasis, whereas deficient mitophagy accelerates the accumulation of damaged mitochondria to mediate the pathologies of NDDs. Therefore, targeting mitophagy has become a valuable therapeutic pathway for the treatment of NDDs. Several mitophagy modulators have been shown to ameliorate neurodegeneration in PD and AD. However, it remains to be further investigated for other NDDs. Here, we describe the mechanism and key signaling pathway of mitophagy and summarize the roles of defective mitophagy on the pathogenesis of NDDs. Further, we underline the development advances of mitophagy modulators for PD and AD therapy, discuss the therapeutic challenges and limitations of the existing modulators, and provide guidelines for mitophagy mechanism exploration and drug design.
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