Nagata Kohzo
Department of Medical Technology, Nagoya University School of Health Sciences, 1-1-20 Daikominami, Higashi-ku, Nagoya 461-8673, Japan.
Curr Hypertens Rep. 2008 Jun;10(3):216-21. doi: 10.1007/s11906-008-0041-y.
Aldosterone provides circulatory support by promoting reabsorption of sodium in exchange for potassium in the kidney. Mineralocorticoid receptors (MRs) are found in nonepithelial (vessel, heart, and brain) and epithelial tissues. Excess aldosterone may exert harmful effects by provoking hypertrophy and fibrosis in the cardiovascular system, thus contributing to reduced vascular compliance and increased ventricular stiffness. Primary aldosteronism is the most common cause of mineralocorticoid-induced hypertension, and MR antagonism offers the best prospect for achieving therapeutic goals. MR blockade also ameliorates pathological changes in the heart in the setting of low-aldosterone hypertension. The beneficial cardiac effects of MR antagonists are likely attributable, at least in part, to attenuation of myocardial oxidative stress and coronary vascular inflammation induced by activation of MRs. MR antagonism thus may have wide therapeutic potential in various cardiovascular diseases, with its benefit not limited to those characterized by aldosterone or salt excess.
醛固酮通过促进肾脏中钠的重吸收以交换钾来提供循环支持。盐皮质激素受体(MRs)存在于非上皮组织(血管、心脏和大脑)和上皮组织中。醛固酮过多可能通过引发心血管系统的肥大和纤维化而产生有害影响,从而导致血管顺应性降低和心室僵硬度增加。原发性醛固酮增多症是盐皮质激素诱导性高血压的最常见原因,而MR拮抗作用为实现治疗目标提供了最佳前景。在低醛固酮性高血压的情况下,MR阻断也可改善心脏的病理变化。MR拮抗剂对心脏的有益作用可能至少部分归因于减轻由MR激活诱导的心肌氧化应激和冠状动脉血管炎症。因此,MR拮抗作用可能在各种心血管疾病中具有广泛的治疗潜力,其益处不限于以醛固酮或盐过量为特征的疾病。