肝损伤
药理学
天冬氨酸转氨酶
氧化应激
肿瘤坏死因子α
鞘氨醇
生物
丙氨酸转氨酶
1-磷酸鞘氨醇
细胞凋亡
受体
生物化学
免疫学
内分泌学
碱性磷酸酶
酶
作者
Mengnan Zeng,Aozi Feng,Lı Wang,Kun Li,Jihong Zhou
标识
DOI:10.1016/j.intimp.2023.110912
摘要
AsA can ameliorate LPS/D-GalN-induced ALI by inhibiting inflammation and oxidative stress via the SPHK1/S1P/S1PR1 pathway. In this way, a molecular justification is provided for AsA application in ALI treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI