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Aldosterone as a Cardiovascular Risk Hormone

机译:醛固酮作为心血管风险激素

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References(88) Cited-By(9) The pathophysiological role of aldosterone in the development of cardiovascular disease has long been considered to be due its potent volume expansion/hypertensive effect mainly via mineralocorticoid receptor (MR) expressed in renal tubular epithelial cells. However, recent accumulating lines of evidence from clinical and experimental studies have suggested that direct cardiovascular effect of aldosterone contributes to the development of cardiovascular injury via MRs in non-epithelial tissue. A series of recent clinical studies have revealed that patients with primary aldosteronism have higher incidence of cardiovascular and renal complications than those with essential hypertension, and that aldosterone antagonism has cardiovascular protective effect in patients with heart failure independent from blood pressure. Numerous experimental studies have shown that both inflammation and oxidative stress play an initial and key role in the development of aldosterone-induced cardiovascular injury via non-epithelial MR activation. In this review, we discuss recent research progress in aldosterone and MR effects, with special emphasis on the pathophysiological role of aldosterone in cardiovascular diseases and the possible molecular mechanism(s) of cardiovascular injury by non-epithelial MR activation.
机译:引用(88)引用(9)醛固酮在心血管疾病发展中的病理物理学作用长期以来一直被认为是主要的产量膨胀/高血压效果主要通过肾小管上皮细胞表达的Mineralocorcoid受体(MR)。然而,来自临床和实验研究的最近积累的证据表明,醛固酮的直接心血管作用有助于通过非上皮组织MRS的心血管损伤的发展。一系列最近的临床研究表明,原发性醛固酮患者的心血管和肾并发症的发病率较高,而且具有必要的高血压,醛固酮对心脏衰竭患者具有心脏血管保护作用,与血压无关。许多实验研究表明,炎症和氧化应力均在通过非上皮先生活化的醛固酮诱导的心血管损伤发展中发挥着初始和关键作用。在本综述中,我们讨论了最近在醛固酮和MR效应中的研究进展,特别强调了醛固酮在心血管疾病中的病理生理作用以及非上皮先生活化的心血管损伤可能的分子机制。

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