Cocaine and amphetamine-regulated transcript improves myocardial ischemia–reperfusion injury through PI3K/AKT signalling pathway

IF 2.9 4区 医学 Q2 Medicine
Yachen Wang, Ziwei Wang, Zeyan Peng, Lifeng Feng, Wencong Tian, Shengzheng Zhang, Lei Cao, Jing Li, Liang Yang, Yang Xu, Yang Gao, Jie Liu, Jie Yan, Xiaodong Ma, Wangchun Sun, Lihong Guo, Xuan Li, Yanna Shen, Zhi Qi
{"title":"Cocaine and amphetamine-regulated transcript improves myocardial ischemia–reperfusion injury through PI3K/AKT signalling pathway","authors":"Yachen Wang,&nbsp;Ziwei Wang,&nbsp;Zeyan Peng,&nbsp;Lifeng Feng,&nbsp;Wencong Tian,&nbsp;Shengzheng Zhang,&nbsp;Lei Cao,&nbsp;Jing Li,&nbsp;Liang Yang,&nbsp;Yang Xu,&nbsp;Yang Gao,&nbsp;Jie Liu,&nbsp;Jie Yan,&nbsp;Xiaodong Ma,&nbsp;Wangchun Sun,&nbsp;Lihong Guo,&nbsp;Xuan Li,&nbsp;Yanna Shen,&nbsp;Zhi Qi","doi":"10.1111/1440-1681.13904","DOIUrl":null,"url":null,"abstract":"<p>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.</p>","PeriodicalId":50684,"journal":{"name":"Clinical and Experimental Pharmacology and Physiology","volume":null,"pages":null},"PeriodicalIF":2.9000,"publicationDate":"2024-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and Experimental Pharmacology and Physiology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1440-1681.13904","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

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.

Abstract Image

可卡因和苯丙胺调控转录本通过 PI3K/AKT 信号通路改善心肌缺血再灌注损伤。
心肌缺血再灌注损伤(MIRI)是急性心肌梗死再灌注治疗中常见的临床症状。有研究表明,可卡因和苯丙胺调控转录物(CART)可改善脑缺血再灌注损伤,但 CART 对 MIRI 的影响尚未得到研究。在本文中,我们发现CART通过抑制细胞凋亡和过度自噬来保护I/R过程中的心脏,这表明CART将成为治疗MIRI的潜在候选药物。进一步的分析表明,CART上调了磷酸-AKT的活化,导致I/R后乳酸脱氢酶(LDH)释放、细胞凋亡、氧化应激和过度自噬的下调,而PI3K抑制剂LY294002抑制了这种下调。总之,CART通过抑制心肌细胞凋亡和过度自噬来减轻MIRI,其保护作用依赖于PI3K/AKT信号通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
6.20
自引率
0.00%
发文量
128
审稿时长
6 months
期刊介绍: Clinical and Experimental Pharmacology and Physiology is an international journal founded in 1974 by Mike Rand, Austin Doyle, John Coghlan and Paul Korner. Our focus is new frontiers in physiology and pharmacology, emphasizing the translation of basic research to clinical practice. We publish original articles, invited reviews and our exciting, cutting-edge Frontiers-in-Research series’.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信