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Research progress on the cardiorenal protection of non-steroid mineralocorticoid receptor antagonists in patients with chronic kidney disease / 生理学报
Acta Physiologica Sinica ; (6): 1023-1030, 2022.
Article in Chinese | WPRIM | ID: wpr-970097
ABSTRACT
Mineralocorticoid receptor antagonists not only are used as a diuretics to treat essential hypertension, but also protect the heart and kidney by inhibiting inflammation and fibrosis. Since the discovery of spironolactone, the first generation of mineralocorticoid receptor antagonist, two types of non-steroid mineralocorticoid receptor antagonists (finerenone and esaxerenone) approved for clinical use have been developed, which have the advantages of high affinity, high selectivity and balanced distribution in heart and kidney, and can be used in clinic as a cardiorenal protective drug. In this paper, the development history of mineralocorticoid receptor antagonists was reviewed, and the pathophysiological mechanism of inflammation and fibrosis caused by mineralocorticoid receptors and the similarities and differences of different generations of mineralocorticoid receptor antagonists were analyzed. In particular, the phase III clinical research evidence of finerenone and esaxerenone was discussed. This paper also reviews the research progress of cardiorenal protection of non-steroid mineralocorticoid receptor antagonists in patients with chronic kidney disease.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Fibrosis / Clinical Trials, Phase III as Topic / Mineralocorticoid Receptor Antagonists / Renal Insufficiency, Chronic / Heart Failure / Mineralocorticoids Limits: Humans Language: Chinese Journal: Acta Physiologica Sinica Year: 2022 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Fibrosis / Clinical Trials, Phase III as Topic / Mineralocorticoid Receptor Antagonists / Renal Insufficiency, Chronic / Heart Failure / Mineralocorticoids Limits: Humans Language: Chinese Journal: Acta Physiologica Sinica Year: 2022 Type: Article