神经保护
表型筛选
表型
药品
药理学
对偶(语法数字)
神经科学
炎症
药物发现
生物
医学
计算生物学
生物信息学
免疫学
遗传学
基因
文学类
艺术
作者
Xuehui Liu,Hong-Yuan Liu,Jing Gu,Mouxin Huang,Qin Ouyang
标识
DOI:10.1021/acschemneuro.5c00123
摘要
Traditional drug development, which predominantly focuses on single target/phenotype evaluation, often fails to achieve optimal therapeutic outcomes in multifactorial and multitarget conditions like ischemia-reperfusion injury. In this viewpoint, we highlight a novel dual-phenotypic drug screening strategy targeting neuronal protective and anti-inflammatory effects for treatment of ischemia-reperfusion injury. This strategy involves the utilization of primary neuron treated with oxygen-glucose deprivation/reoxygenation (OGD/R), lipopolysaccharide (LPS)-activated microglial models and coculture systems or brain organoids as in vitro models, as well as mouse middle cerebral artery occlusion/reperfusion (MCAO/R) models for in vivo evaluation. The dual-phenotypic drug screening strategies marks a paradigm shift from single-factorial approach to a system biology-based integrated methodology, offering significant advantages for developing therapies for the complex multifactorial disease ischemia-reperfusion injury.
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