重编程
前列腺素
医学
肺
药理学
化学
内科学
生物化学
细胞
作者
Xishuai Wang,Shaojun Nong,Qingshan Zheng,Zhao Congcong,Chao Yi,Song Li,Lunan Zhao,Xiliang Kong,Yuehui Zhou,Depeng Dong,Weina Niu,Zhuo Chen,Cong Liu,Wei Zhao,Zhuo Sun,Jie Wei,Yang Lv,Lichang Yang,Xin Jin,Shanshan Cai
标识
DOI:10.1016/j.freeradbiomed.2025.06.024
摘要
AE pretreatment confers protection against ALI by orchestrating metabolic reprogramming to enhance anti-inflammatory responses. AE pretreatment attenuates LPS-induced ALI by reprogramming linoleic acid and arachidonic acid metabolism, thereby suppressing 6-keto-PGF1α biosynthesis. Pharmacological inhibition of 6-keto-PGF1α significantly alleviated ALI severity and mortality. These findings highlight AE as a preventive strategy and identify 6-keto-PGF1α as a therapeutic target for inflammatory lung injury.
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