神经保护
创伤性脑损伤
小胶质细胞
谷氨酸受体
脂质过氧化
药理学
KEAP1型
星形胶质细胞
活性氧
化学
氧化应激
医学
生物化学
内科学
炎症
中枢神经系统
转录因子
受体
精神科
基因
作者
Hongxing Tang,Kejun He,Kun Zhao,Zheng Chen,Wei‐Chi Wu,Weilin Jin,Lixuan Yang,Baoshu Xie
标识
DOI:10.1089/neu.2023.0150
摘要
In this study, we investigated the effects of hinokitiol, a small-molecule natural compound, against neuronal ferroptosis after traumatic brain injury (TBI). A controlled cortical impact (CCI) mouse model and excess glutamate-treated HT-22 cells were used to study the effects of hinokitiol on TBI. Hinokitiol mitigated TBI brain tissue lesions and significantly improved neurological function. Neuron loss and iron deposition were ameliorated after hinokitiol administration. Hinokitiol alleviated excessive glutamate-induced intracellular reactive oxygen species (ROS), lipid peroxidation, and Fe
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