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

Author:

Wang Yachen12,Wang Ziwei13,Peng Zeyan1,Feng Lifeng1,Tian Wencong14,Zhang Shengzheng1,Cao Lei4,Li Jing1,Yang Liang14,Xu Yang1,Gao Yang14,Liu Jie1,Yan Jie1,Ma Xiaodong5,Sun Wangchun5,Guo Lihong6,Li Xuan2,Shen Yanna7,Qi Zhi13468

Affiliation:

1. Department of Molecular Pharmacology, School of Medicine Nankai University Tianjin China

2. Tianjin Eye Hospital, Tianjin Key Laboratory of Ophthalmology and Visual Science Tianjin Eye Institute Tianjin China

3. NanKai University Eye Institute Tianjin China

4. Tianjin Key Laboratory of General Surgery in Construction Tianjin Union Medical Center Tianjin China

5. Fifth People's Hospital of Dongying Shandong China

6. Shengli Oilfield Central Hospital Gastrointestinal Disease Research Institute Shandong China

7. School of Medical Technology Tianjin Medical University Tianjin China

8. Xinjiang Production and Construction Corps Hospital Xinjiang China

Abstract

AbstractMyocardial 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.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Tianjin Municipality

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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