Health position paper and redox perspectives on reactive oxygen species as signals and targets of cardioprotection.
Cardioprotection
Infarct size
Ischemic conditioning
Mitochondrion
Myocardial infarction
Myocardial ischemia
Reperfusion
Journal
Redox biology
ISSN: 2213-2317
Titre abrégé: Redox Biol
Pays: Netherlands
ID NLM: 101605639
Informations de publication
Date de publication:
11 2023
11 2023
Historique:
received:
20
07
2023
revised:
04
09
2023
accepted:
15
09
2023
medline:
30
10
2023
pubmed:
16
10
2023
entrez:
15
10
2023
Statut:
ppublish
Résumé
The present review summarizes the beneficial and detrimental roles of reactive oxygen species in myocardial ischemia/reperfusion injury and cardioprotection. In the first part, the continued need for cardioprotection beyond that by rapid reperfusion of acute myocardial infarction is emphasized. Then, pathomechanisms of myocardial ischemia/reperfusion to the myocardium and the coronary circulation and the different modes of cell death in myocardial infarction are characterized. Different mechanical and pharmacological interventions to protect the ischemic/reperfused myocardium in elective percutaneous coronary interventions and coronary artery bypass grafting, in acute myocardial infarction and in cardiotoxicity from cancer therapy are detailed. The second part keeps the focus on ROS providing a comprehensive overview of molecular and cellular mechanisms involved in ischemia/reperfusion injury. Starting from mitochondria as the main sources and targets of ROS in ischemic/reperfused myocardium, a complex network of cellular and extracellular processes is discussed, including relationships with Ca
Identifiants
pubmed: 37839355
pii: S2213-2317(23)00295-1
doi: 10.1016/j.redox.2023.102894
pmc: PMC10590874
pii:
doi:
Substances chimiques
Reactive Oxygen Species
0
Types de publication
Journal Article
Review
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
102894Subventions
Organisme : British Heart Foundation
ID : PG/16/85/32471
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/18/44/33790
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/19/51/34493
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/21/10798
Pays : United Kingdom
Organisme : Medical Research Council
ID : G00913
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RG/19/11/34633
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/18/2/34213
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CH/1999001/11735
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/18/2/34213
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : R01 HL128831
Pays : United States
Informations de copyright
Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest PF is the founder and CEO of Pharmahungary Group, a group of R&D companies. AMS is an adviser to Forcefield Therapeutics and CYTE – Global Network for Clinical Research and sits on the Board of Heqet Therapeutics. CM served as an advisor to Amgen, Boehringer Ingelheim, Bristol Myers Squibb, NovoNordisk and Servier and received speaker honoraria from AstraZeneca, Bayer, Bristol Myers Squibb, Boehringer Ingelheim, Berlin Chemie, Novartis and NovoNordisk. No other author had an interest to declare.