Mitochondrial drug targets in neurodegenerative diseases

被引:20
作者
Lee, Jiyoun [1 ]
机构
[1] Sungshin Univ, Dept Global Med Sci, Seoul 142732, South Korea
关键词
Mitochondria; Neurodegenerative diseases; Mitochondrial dysfunction; Mitochondria permeability transition pore (mPTP); Chaperones; Kinases; Proteases; PERMEABILITY TRANSITION PORE; ADENINE-NUCLEOTIDE TRANSLOCASE; AMYOTROPHIC-LATERAL-SCLEROSIS; DEPENDENT ANION CHANNEL; PROTEIN; 18; KDA; 17-BETA-HYDROXYSTEROID-DEHYDROGENASE TYPE 10; ISOLATED LIVER-MITOCHONDRIA; AMYLOID PRECURSOR PROTEIN; CALCIUM-ION ACCUMULATION; STRUCTURE-BASED DESIGN;
D O I
10.1016/j.bmcl.2015.11.032
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Growing evidence suggests that mitochondrial dysfunction is the main culprit in neurodegenerative diseases. Given the fact that mitochondria participate in diverse cellular processes, including energetics, metabolism, and death, the consequences of mitochondrial dysfunction in neuronal cells are inevitable. In fact, new strategies targeting mitochondrial dysfunction are emerging as potential alternatives to current treatment options for neurodegenerative diseases. In this review, we focus on mitochondrial proteins that are directly associated with mitochondrial dysfunction. We also examine recently identified small molecule modulators of these mitochondrial targets and assess their potential in research and therapeutic applications. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:714 / 720
页数:7
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