神经炎症
柠檬酸循环
IDH1
小胶质细胞
异柠檬酸脱氢酶
线粒体
神经退行性变
代谢途径
生物
细胞生物学
下调和上调
细胞内
神经保护
胞浆
丙酮酸脱氢酶复合物
生物化学
表观遗传学
神经科学
癌症研究
化学
酶
焊剂(冶金)
氧化磷酸化
糖酵解
PI3K/AKT/mTOR通路
平衡
认知功能衰退
药理学
疾病
乌头酸酶
新陈代谢
作者
Qianqian Li,Yajin Liao,Yan‐Bo Zhao,Hongxing Wu,Tong Jin,Shuoshuo Li,Yuhan Liu,Peng Li,Songying Ouyang,Zekai Li,Yuting Xia,Qian Hua,Rui‐Yuan Pan,Zengqiang Yuan
摘要
Dysregulated tricarboxylic acid (TCA) cycle activity is increasingly recognized as a contributor to Alzheimer's disease (AD) pathogenesis, yet the mechanistic underpinnings of the relationship remain unclear. Here, we identify isocitrate dehydrogenase 1 (IDH1), a key enzyme in the TCA cycle, as a critical pathogenic driver of AD in microglia. IDH1 expression was markedly upregulated in microglia from both AD patients and 5×FAD mice. Elevated IDH1 promoted excessive cytosolic citrate consumption, which restricted citrate shuttling into mitochondria and impaired mitochondrial TCA cycle function. This citrate metabolic imbalance further disrupted epigenetic regulation, thereby exacerbating AD-related pathological processes. Using structure-based screening and co-crystallization analysis, we identified Kinsenoside (KIN), a natural small molecule, as a selective competitive inhibitor of IDH1 that binds to its isocitrate-binding pocket. Targeting IDH1 with KIN inhibited its activity, which restored intracellular citrate distribution, reactivated mitochondrial TCA cycle flux, and reestablished metabolic homeostasis. Notably, this intervention not only attenuated neuroinflammation but also reduced β-amyloid (Aβ) deposition and significantly improved cognitive performance in 5×FAD mice. Collectively, our findings establish IDH1-mediated metabolic dysregulation as a pivotal pathogenic mechanism in AD and highlight KIN as a promising therapeutic candidate by targeting microglial IDH1 to restore metabolic and functional homeostasis.
科研通智能强力驱动
Strongly Powered by AbleSci AI