对乙酰氨基酚
肝细胞
蛋白激酶B
化学
体内
下调和上调
福克斯O1
肝损伤
β氧化
药理学
生物化学
体外
医学
生物
信号转导
酶
基因
生物技术
作者
Shuai Chen,Zhi Lü,Haoyu Jia,Bo Yang,Chun Liu,Yuxin Yang,Shuo Zhang,Zhijing Wang,Liu Yang,Shanshan Li,Jing Li,Changqing Yang
标识
DOI:10.1016/j.jhep.2022.10.028
摘要
Mas signalling arises as a novel therapeutic target for patients with APAP-induced liver injury. The Mas-AKT/FOXO1-fatty acid degradation pathway could be critical for the development of treatment strategies for APAP overdose. When Mas signalling is targeted, the extent of liver injury should be considered at the time of administration. These findings obtained from APAP-challenged mice still need to be confirmed in a clinical context.
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