神经保护
肌萎缩侧索硬化
激酶
LRRK2
神经科学
体内
疾病
药理学
帕金森病
化学
生物
医学
生物化学
内科学
生物技术
作者
Ricardo Alberto Moreno,Javier Bueno,Santiago Barber,Carmen Gil,Ana Martı́nez
标识
DOI:10.1016/j.ejmech.2023.115511
摘要
Selective and brain-permeable protein kinase inhibitors are in preclinical development for treating neurodegenerative diseases. Among them, MLK3 inhibitors, with a potent neuroprotective biological action have emerged as valuable agents for the treatment of pathologies such as Alzheimer's, Parkinson's disease and amyotrophic lateral sclerosis. In fact, one MLK3 inhibitor, CEP-1347, reached clinical trials for Parkinson's disease. Additionally, another compound called prostetin/12k, a potent and rather selective MLK3 inhibitor has started clinical development for ALS based on its motor neuron protection in both in vitro and in vivo models. In this review, we will focus on the role of MLK3 in neuron-related cell death processes, neurodegenerative diseases, and the potential advantages of targeting this kinase through pharmacological modulation for neuroprotective treatment.
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