Department of Clinical Laboratory, School of Medicine, The University of Tokyo, Tokyo, Japan.
Hypertens Res. 2013 Aug;36(8):657-60. doi: 10.1038/hr.2013.69.
High salt intake is a risk for developing resistant hypertension, and even under triple therapy with diuretics, an angiotensin-converting enzyme inhibitor/angiotensin receptor blocker and a calcium channel blocker, the volume is occasionally not controlled. In such cases, a mineralocorticoid receptor (MR) antagonist additively lowers the circulating blood volume and blood pressure despite the lower circulating aldosterone level. This mechanism may be explained by the increase in the number of MR under some conditions or the activation of these receptors independent of aldosterone. Future diagnostic tools to evaluate receptor activity may be valuable for the proper diagnosis and choice of therapy. Additionally, basic research has suggested that oxidative stress and the renin-angiotensin-aldosterone system in the brain represent new targets for the treatment of resistant hypertension.
高盐摄入是导致耐药性高血压的一个风险因素,即使在利尿剂、血管紧张素转换酶抑制剂/血管紧张素受体阻滞剂和钙通道阻滞剂三联治疗下,有时也无法控制容量。在这种情况下,尽管循环醛固酮水平较低,盐皮质激素受体 (MR) 拮抗剂仍可额外降低循环血量和血压。这种机制可能是由于在某些情况下 MR 数量增加,或者这些受体独立于醛固酮而被激活。未来评估受体活性的诊断工具可能对正确诊断和治疗选择有价值。此外,基础研究表明,大脑中的氧化应激和肾素-血管紧张素-醛固酮系统是治疗耐药性高血压的新靶点。