The cardioprotective effects of carvedilol on ischemia and reperfusion injury by AMPK signaling pathway
Carvedilol, a third generation beta blocker, is in clinical use for heart failure patients. However, besides adrenergic receptor blockade, the pharmacological effects of carvedilol on cardiomyocytes remain unknown. AMP-activated protein kinase (AMPK) is an emerging target recognized for heart failur...
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doaj-61a9babb750046d295c1a97ff6558ee12021-05-20T07:38:39ZengElsevierBiomedicine & Pharmacotherapy0753-33222019-09-01117The cardioprotective effects of carvedilol on ischemia and reperfusion injury by AMPK signaling pathwayHaiyan Hu0Xuan Li1Di Ren2Yi Tan3Jimei Chen4Lei Yang5Ruiping Chen6Ji Li7Ping Zhu8Department of Cardiac surgery, Affiliated of South China Hospital, Southern Medical University (Guangdong Provincial People's Hospital), Southern Medical University/The Second School of Clinical Medicine, Guangzhou 510515, China; Department of Physiology and Biophysics, Mississippi Center for Heart Research, University of Mississippi Medical Center, Jackson, MS, United States; Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, ChinaDepartment of Physiology and Biophysics, Mississippi Center for Heart Research, University of Mississippi Medical Center, Jackson, MS, United StatesDepartment of Physiology and Biophysics, Mississippi Center for Heart Research, University of Mississippi Medical Center, Jackson, MS, United StatesPediatric Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY, United states; Wendy L. Novak Diabetes Care Center, Louisville, KY, United StatesGuangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, ChinaGuangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, ChinaGuangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, ChinaDepartment of Physiology and Biophysics, Mississippi Center for Heart Research, University of Mississippi Medical Center, Jackson, MS, United StatesDepartment of Cardiac surgery, Affiliated of South China Hospital, Southern Medical University (Guangdong Provincial People's Hospital), Southern Medical University/The Second School of Clinical Medicine, Guangzhou 510515, China; Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, China; Corresponding author at: Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, 510080, China.Carvedilol, a third generation beta blocker, is in clinical use for heart failure patients. However, besides adrenergic receptor blockade, the pharmacological effects of carvedilol on cardiomyocytes remain unknown. AMP-activated protein kinase (AMPK) is an emerging target recognized for heart failure treatment. The mechanical properties and intracellular Ca2+ properties were measured in isolated cardiomyocyte contractile functions in response to ischemic stress. Treatment of cardiomyocytes with carvedilol augmented phosphorylation of AMPK and downstream acetyl CoA carboxylase (ACC), and ameliorated hypoxia-induced impairment in maximal velocity of shortening (+dL/dt) and relengthening (-dL/dt), and the impaired peak height and peak shortening (PS) amplitude caused by hypoxia. Carvedilol treatment improved calcium homeostasis with rescuing the peak Ca2+ signal, the maximum rate of Ca2+ change during contraction (+dF/dt) and the maximum rate of Ca2+ change during relaxation (-dF/dt) under hypoxia conditions. In mouse hearts perfused ex vivo with carvedilol, the function of post-ischemia left ventricle was improved and an augmentation in myocardial glucose uptake and glucose oxidation, and inhibition of fatty acid oxidation during ischemia and reperfusion. The protective effect of carvedilol was further supported in an in vivo regional ischemia model by ligation of left anterior descending coronary artery (LAD), mice treated with carvedilol followed by LAD occlusion and reperfusion showed significant size reduction in infarcted myocardium and improved cardiac functions. Therefore, Carvedilol as a clinical drug can modulate cardiac AMPK signaling pathway to reduce ischemic insults by ischemia and reperfusion.http://www.sciencedirect.com/science/article/pii/S075333221932236XAMPKCarvedilolCardioprotectionIschemia/reperfusion |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Haiyan Hu Xuan Li Di Ren Yi Tan Jimei Chen Lei Yang Ruiping Chen Ji Li Ping Zhu |
spellingShingle |
Haiyan Hu Xuan Li Di Ren Yi Tan Jimei Chen Lei Yang Ruiping Chen Ji Li Ping Zhu The cardioprotective effects of carvedilol on ischemia and reperfusion injury by AMPK signaling pathway Biomedicine & Pharmacotherapy AMPK Carvedilol Cardioprotection Ischemia/reperfusion |
author_facet |
Haiyan Hu Xuan Li Di Ren Yi Tan Jimei Chen Lei Yang Ruiping Chen Ji Li Ping Zhu |
author_sort |
Haiyan Hu |
title |
The cardioprotective effects of carvedilol on ischemia and reperfusion injury by AMPK signaling pathway |
title_short |
The cardioprotective effects of carvedilol on ischemia and reperfusion injury by AMPK signaling pathway |
title_full |
The cardioprotective effects of carvedilol on ischemia and reperfusion injury by AMPK signaling pathway |
title_fullStr |
The cardioprotective effects of carvedilol on ischemia and reperfusion injury by AMPK signaling pathway |
title_full_unstemmed |
The cardioprotective effects of carvedilol on ischemia and reperfusion injury by AMPK signaling pathway |
title_sort |
cardioprotective effects of carvedilol on ischemia and reperfusion injury by ampk signaling pathway |
publisher |
Elsevier |
series |
Biomedicine & Pharmacotherapy |
issn |
0753-3322 |
publishDate |
2019-09-01 |
description |
Carvedilol, a third generation beta blocker, is in clinical use for heart failure patients. However, besides adrenergic receptor blockade, the pharmacological effects of carvedilol on cardiomyocytes remain unknown. AMP-activated protein kinase (AMPK) is an emerging target recognized for heart failure treatment. The mechanical properties and intracellular Ca2+ properties were measured in isolated cardiomyocyte contractile functions in response to ischemic stress. Treatment of cardiomyocytes with carvedilol augmented phosphorylation of AMPK and downstream acetyl CoA carboxylase (ACC), and ameliorated hypoxia-induced impairment in maximal velocity of shortening (+dL/dt) and relengthening (-dL/dt), and the impaired peak height and peak shortening (PS) amplitude caused by hypoxia. Carvedilol treatment improved calcium homeostasis with rescuing the peak Ca2+ signal, the maximum rate of Ca2+ change during contraction (+dF/dt) and the maximum rate of Ca2+ change during relaxation (-dF/dt) under hypoxia conditions. In mouse hearts perfused ex vivo with carvedilol, the function of post-ischemia left ventricle was improved and an augmentation in myocardial glucose uptake and glucose oxidation, and inhibition of fatty acid oxidation during ischemia and reperfusion. The protective effect of carvedilol was further supported in an in vivo regional ischemia model by ligation of left anterior descending coronary artery (LAD), mice treated with carvedilol followed by LAD occlusion and reperfusion showed significant size reduction in infarcted myocardium and improved cardiac functions. Therefore, Carvedilol as a clinical drug can modulate cardiac AMPK signaling pathway to reduce ischemic insults by ischemia and reperfusion. |
topic |
AMPK Carvedilol Cardioprotection Ischemia/reperfusion |
url |
http://www.sciencedirect.com/science/article/pii/S075333221932236X |
work_keys_str_mv |
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