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...

Full description

Bibliographic Details
Main Authors: Haiyan Hu, Xuan Li, Di Ren, Yi Tan, Jimei Chen, Lei Yang, Ruiping Chen, Ji Li, Ping Zhu
Format: Article
Language:English
Published: Elsevier 2019-09-01
Series:Biomedicine & Pharmacotherapy
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S075333221932236X
id doaj-61a9babb750046d295c1a97ff6558ee1
record_format Article
spelling 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 AT haiyanhu thecardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT xuanli thecardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT diren thecardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT yitan thecardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT jimeichen thecardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT leiyang thecardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT ruipingchen thecardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT jili thecardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT pingzhu thecardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT haiyanhu cardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT xuanli cardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT diren cardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT yitan cardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT jimeichen cardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT leiyang cardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT ruipingchen cardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT jili cardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
AT pingzhu cardioprotectiveeffectsofcarvedilolonischemiaandreperfusioninjurybyampksignalingpathway
_version_ 1721435219529039872