Dutzmann Jochen, Bauersachs Johann, Sedding Daniel G
Dept. of Cardiology and Angiology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.
Dept. of Cardiology and Angiology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.
Vascul Pharmacol. 2017 Dec 21. doi: 10.1016/j.vph.2017.12.065.
Mineralocorticoid receptor antagonists (MRAs), such as spironolactone and eplerenone have an established role in the treatment of heart failure. However, many experimental and clinical studies have shown that aldosterone also plays a pivotal role in a variety of other pathophysiological conditions within the cardiovascular system. Aldosterone has been suggested to promote inflammation, endothelial dysfunction and smooth muscle cell hyperplasia during the development of atherosclerosis, thereby promoting the development of coronary artery disease (CAD). Since CAD and subsequent ischemic cardiomyopathy are the major causes of heart failure, it is of major interest, whether pharmacological therapy with MRAs among heart failure patients will also affect the common underlying conditions, namely, atherosclerosis and subsequent coronary vessel narrowing/rarefication. Therefore, in this article, we reviewed and discussed the preclinical and clinical evidence of MRAs for the treatment of acute or chronic vascular remodeling processes, such as atherosclerosis and post-angioplasty restenosis, which determine the progression of CAD and subsequent ischemic cardiomyopathy.
盐皮质激素受体拮抗剂(MRAs),如螺内酯和依普利酮,在心力衰竭治疗中具有既定作用。然而,许多实验和临床研究表明,醛固酮在心血管系统内的多种其他病理生理状况中也起着关键作用。有人提出,醛固酮在动脉粥样硬化发展过程中会促进炎症、内皮功能障碍和平滑肌细胞增生,从而促进冠状动脉疾病(CAD)的发展。由于CAD及随后的缺血性心肌病是心力衰竭的主要原因,心力衰竭患者使用MRAs进行药物治疗是否也会影响常见的潜在病症,即动脉粥样硬化及随后的冠状动脉狭窄/稀疏,这一点备受关注。因此,在本文中,我们回顾并讨论了MRAs用于治疗急性或慢性血管重塑过程(如动脉粥样硬化和血管成形术后再狭窄)的临床前和临床证据,这些过程决定了CAD及随后缺血性心肌病的进展。