炎症
心肌保护
医学
发病机制
再灌注损伤
缺血
心肌梗塞
生物信息学
机制(生物学)
神经科学
免疫学
心脏病学
生物
认识论
哲学
作者
Anna De Bartolo,Naomi Romeo,Tommaso Angelone,Carmine Rocca
摘要
ABSTRACT Aim Timely myocardial reperfusion is essential for restoring blood flow to post‐ischemic tissue, thereby reducing cardiac injury and limiting infarct size. However, this process can paradoxically result in additional, irreversible myocardial damage, known as myocardial ischemia–reperfusion injury (MIRI). The goal of this review is to explore the role of specialized pro‐resolving mediators (SPMs) in atherosclerosis and MIRI, and to assess the therapeutic potential of targeting inflammation resolution in these cardiovascular conditions. Methods This review summarizes current preclinical and clinical evidence on the involvement of SPMs in the pathogenesis of atherosclerosis and MIRI, acknowledging that several cellular and molecular aspects of their mechanisms of action remain to be fully elucidated. Results MIRI is a complex phenomenon in which inflammation, initially triggered during ischemia and further amplified upon reperfusion, plays a central role in its pathogenesis. Various cellular and molecular players mediate the initial pro‐inflammatory response and the subsequent anti‐inflammatory reparative phase following acute myocardial infarction (AMI), contributing both to ischemia‐ and reperfusion‐induced damage as well as to the healing process. SPMs have emerged as key endogenous immunoresolvents with potent anti‐inflammatory, antioxidant, and pro‐resolving properties that contribute to limit excessive acute inflammation and promote tissue repair. While dysregulated SPM‐related signaling has been linked to various cardiovascular diseases (CVD), their precise role in AMI and MIRI remains incompletely understood. Conclusion Targeting inflammation resolution may represent a promising therapeutic strategy for mitigating atheroprogression and addressing a complex condition such as MIRI.
科研通智能强力驱动
Strongly Powered by AbleSci AI