Guangzhou Institutes of Biomedicine & Health, Chinese Academy of Sciences, Guangzhou 510530, People's Republic of China.
Future Med Chem. 2013 Sep;5(13):1559-71. doi: 10.4155/fmc.13.125.
Alzheimer's disease (AD) is complicated and difficult to fully understand, it might need multiple drug-discovery strategies to combat the disease. Regardless of the cause of AD, neuronal death in the brain plays a key role in AD progression and is directly linked to neuroinflammation. Thus, the regulation of neuroinflammatory processes might be a practical strategy for the treatment of AD. This review highlights the development of anti-neuroinflammatory agents that have shown promise in vitro or in vivo by attenuating microglial activation or cognitive decline. The agents are categorized based on the related signaling pathways, including the receptor for advanced glycation end products, p38 MAPKs, NF-κB and peroxisome proliferator-activated receptor γ; and inhibitors against microglial activation lacking clear mechanisms. These anti-neuroinflammatory agents support the concept and represent important chemical probes for the development of anti-neuroinflammatory drugs for the treatment of AD.
阿尔茨海默病(AD)是一种复杂且难以完全理解的疾病,可能需要多种药物发现策略来对抗这种疾病。无论 AD 的原因是什么,大脑中的神经元死亡在 AD 的进展中起着关键作用,并且与神经炎症直接相关。因此,调节神经炎症过程可能是治疗 AD 的一种实用策略。本综述强调了通过减轻小胶质细胞激活或认知能力下降而在体外或体内显示出前景的抗神经炎症剂的发展。这些药物根据相关信号通路进行分类,包括晚期糖基化终产物受体、p38MAPKs、NF-κB 和过氧化物酶体增殖物激活受体 γ;以及缺乏明确机制的针对小胶质细胞激活的抑制剂。这些抗神经炎症剂支持这一概念,并代表了用于治疗 AD 的抗神经炎症药物开发的重要化学探针。