自噬
PI3K/AKT/mTOR通路
下调和上调
LY294002型
推车
心肌保护
蛋白激酶B
背景(考古学)
细胞凋亡
缺血
再灌注损伤
药理学
氧化应激
医学
化学
生物
内科学
内分泌学
生物化学
古生物学
工程类
基因
机械工程
作者
Yachen Wang,Ziwei Wang,Zeyan Peng,Lifeng Feng,Wencong Tian,Shengzheng Zhang,Lei Cao,Jing Li,Yang Liang,Yang Xu,Yang Gao,Jie Liu,Jie Yan,Xiaodong Ma,Wangchun Sun,Lihong Guo,Xuan Li,Yanna Shen,Zhi Qi
标识
DOI:10.1111/1440-1681.13904
摘要
Abstract Myocardial ischemia–reperfusion injury (MIRI) is a common clinic scenario that occurs in the context of reperfusion therapy for acute myocardial infarction. It has been shown that cocaine and amphetamine‐regulated transcript (CART) can ameliorate cerebral ischemia–reperfusion (I/R) injury, but the effect of CART on MIRI has not been studied yet. Here, we revealed that CART protected the heart during I/R process by inhibiting apoptosis and excessive autophagy, indicating that CART would be a potential drug candidate for the treatment of MIRI. Further analysis showed that CART upregulated the activation of phospho‐AKT, leading to downregulation of lactate dehydrogenase (LDH) release, apoptosis, oxidative stress and excessive autophagy after I/R, which was inhibited by PI3K inhibitor, LY294002. Collectively, CART attenuated MIRI through inhibition of cardiomyocytes apoptosis and excessive autophagy, and the protective effect was dependent on PI3K/AKT signalling pathway.
科研通智能强力驱动
Strongly Powered by AbleSci AI