神经科学
受体
阿尔茨海默病
疾病
医学
核受体
生物
生物信息学
内科学
转录因子
生物化学
基因
作者
Shweta Mandrekar-Colucci,Gary E. Landreth
标识
DOI:10.1517/14728222.2011.594043
摘要
Nuclear receptors are attractive targets for the treatment of AD due to their ability to facilitate degradation of Aβ, affect microglial activation and suppress the inflammatory milieu of the brain. Liver X receptor agonists have proven difficult to move into clinical trials as long-term treatment results in hepatic steatosis. It is our view that PPAR-γ activation remains a promising avenue for the treatment for AD; however, the poor BBB permeability of the currently available agonists and the negative outcome of the Phase III clinical trials are likely to diminish interest in pursuing this target.
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