JNK3 inhibitors as promising pharmaceuticals with neuroprotective properties

被引:2
|
作者
Wu, Yibeini [1 ]
Zhao, Yiling [2 ]
Guan, Ziman [1 ]
Esmaeili, Sajjad [1 ]
Xiao, Zhicheng [1 ,2 ]
Kuriakose, Diji [1 ]
机构
[1] Monash Univ, Dept Anat & Dev Biol, Clayton, Vic 3800, Australia
[2] Zhejiang Univ, Shaoxing Inst, Shaoxing, Peoples R China
关键词
Apoptosis; inhibitor; JNK3; MAPK signalling pathway; neurodegenerative disease; neuroinflammation; neuroprotection; oxidative stress; SELECTIVE INHIBITORS; PATHWAYS; APOPTOSIS; POTENT; ACTIVATION; THERAPY; DESIGN; DAMAGE; CELLS;
D O I
10.1080/19336918.2024.2316576
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The intensive study and investigation of neuroprotective therapy for central nervous system (CNS) diseases is ongoing. Due to shared mechanisms of neurodegeneration, a neuroprotective approach might offer benefits across multiple neurological disorders, despite variations in symptoms or injuries. C-Jun N-terminal Kinase 3 (JNK3) is found primarily in the CNS and is involved in physiological processes such as brain development, synapse formation, and memory formation. The potential of JNK3 as a target for pharmacological development holds promise for advancing neuroprotective therapies. Developing small molecule JNK3 inhibitors into drugs with neuroprotective qualities could facilitate neuronal restoration and self-repair. This review focuses on elucidating key neuroprotective mechanisms, exploring the interplay between neurodegenerative diseases and neuroprotection, and discussing advancements in JNK3 inhibitor drug development.
引用
收藏
页码:1 / 11
页数:11
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