盐皮质激素受体
依普利酮
螺内酯
盐皮质激素
医学
内皮素受体拮抗剂
敌手
醛固酮
肾脏疾病
受体拮抗剂
内分泌学
内皮素受体
内科学
药理学
受体
作者
Pingping Yang,Tianlun Huang,Gaosi Xu
标识
DOI:10.1016/j.metabol.2016.06.001
摘要
Patients with diabetic kidney disease (DKD) who received angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) may show high serum levels of aldosterone. Finerenone (BAY 94-8862), a novel non-steroidal mineralocorticoid receptor antagonist (MRA), which is more selective for the mineralocorticoid receptor (MR) than spironolactone and has greater affinity for the MR than eplerenone, can reduce the concentration of aldosterone. The interaction between aldosterone and endothelin, together with their regulation on inflammation, oxidative stress and fibrosis, indicates that finerenone combined with atrasentan may play synergetic roles in reversing the procession of DKD. The present review, for the first time, discussed the mechanisms of finerenone combination with ACEI, ARBs, statins, and the endothelin receptor antagonist atrasentan.
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