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心肌细胞衰老与心脏保护:欧洲心脏病学会心脏细胞生物学和心肌功能工作组共识文件

Cardiomyocyte ageing and cardioprotection: consensus document from the ESC working groups cell biology of the heart and myocardial function.

作者信息

Ruiz-Meana Marisol, Bou-Teen Diana, Ferdinandy Péter, Gyongyosi Mariann, Pesce Maurizio, Perrino Cinzia, Schulz Rainer, Sluijter Joost P G, Tocchetti Carlo G, Thum Thomas, Madonna Rosalinda

机构信息

Department of Cardiology, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Universitat Autonoma de Barcelona and Centro de Investigación Biomédica en Red-CV, CIBER-CV, Madrid, Spain.

Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.

出版信息

Cardiovasc Res. 2020 Sep 1;116(11):1835-1849. doi: 10.1093/cvr/cvaa132.

Abstract

Advanced age is a major predisposing risk factor for the incidence of coronary syndromes and comorbid conditions which impact the heart response to cardioprotective interventions. Advanced age also significantly increases the risk of developing post-ischaemic adverse remodelling and heart failure after ischaemia/reperfusion (IR) injury. Some of the signalling pathways become defective or attenuated during ageing, whereas others with well-known detrimental consequences, such as glycoxidation or proinflammatory pathways, are exacerbated. The causative mechanisms responsible for all these changes are yet to be elucidated and are a matter of active research. Here, we review the current knowledge about the pathophysiology of cardiac ageing that eventually impacts on the increased susceptibility of cells to IR injury and can affect the efficiency of cardioprotective strategies.

摘要

高龄是冠状动脉综合征及合并症发病的主要易感风险因素,这些合并症会影响心脏对心脏保护干预措施的反应。高龄还会显著增加缺血后不良重塑及缺血/再灌注(IR)损伤后发生心力衰竭的风险。衰老过程中,一些信号通路会出现缺陷或减弱,而另一些已知会产生有害后果的通路,如糖氧化或促炎通路,则会加剧。导致所有这些变化的致病机制尚待阐明,仍是积极研究的课题。在此,我们综述了目前关于心脏衰老病理生理学的知识,心脏衰老最终会影响细胞对IR损伤的易感性增加,并可能影响心脏保护策略的有效性。

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