Institute of Molecular Cardiovascular Research, RWTH Aachen University, Germany (A.C., K.Q., Z.W., V.J., J.J.).
Department of Internal Medicine and Pediatrics, Nephrology Section, University Hospital, Ghent, Belgium (R.V.).
Circ Res. 2024 Mar;134(5):592-613. doi: 10.1161/CIRCRESAHA.123.324001. Epub 2024 Feb 29.
The crosstalk of the heart with distant organs such as the lung, liver, gut, and kidney has been intensively approached lately. The kidney is involved in (1) the production of systemic relevant products, such as renin, as part of the most essential vasoregulatory system of the human body, and (2) in the clearance of metabolites with systemic and organ effects. Metabolic residue accumulation during kidney dysfunction is known to determine cardiovascular pathologies such as endothelial activation/dysfunction, atherosclerosis, cardiomyocyte apoptosis, cardiac fibrosis, and vascular and valvular calcification, leading to hypertension, arrhythmias, myocardial infarction, and cardiomyopathies. However, this review offers an overview of the uremic metabolites and details their signaling pathways involved in cardiorenal syndrome and the development of heart failure. A holistic view of the metabolites, but more importantly, an exhaustive crosstalk of their known signaling pathways, is important for depicting new therapeutic strategies in the cardiovascular field.
最近,人们对心脏与肺部、肝脏、肠道和肾脏等远距离器官之间的串扰进行了深入研究。肾脏参与(1)全身相关产物的产生,如肾素,作为人体最重要的血管调节系统的一部分,以及(2)清除具有全身和器官作用的代谢物。已知肾功能障碍期间代谢物的积累会导致心血管病理,如内皮细胞激活/功能障碍、动脉粥样硬化、心肌细胞凋亡、心肌纤维化以及血管和瓣膜钙化,从而导致高血压、心律失常、心肌梗死和心肌病。然而,这篇综述概述了尿毒症代谢物,并详细介绍了它们在心肾综合征和心力衰竭发展中涉及的信号通路。对代谢物进行全面的了解,更重要的是,对其已知信号通路的详尽串扰,对于描述心血管领域的新治疗策略非常重要。
Crit Care. 2014-1-6
Am J Physiol Heart Circ Physiol. 2017-7-1
Heart Fail Rev. 2016-3
Interv Cardiol Clin. 2023-10
Toxins (Basel). 2020-3-5
Toxins (Basel). 2020-9-29
Circ Res. 2012-11-9
Am J Physiol Renal Physiol. 2021-4-1
Circulation. 2018-8-28
Toxins (Basel). 2024-10-28
Arterioscler Thromb Vasc Biol. 2024-12