Mineralocorticoid Receptor Blockers: Novel Selective Nonsteroidal Mineralocorticoid Receptor Antagonists.
Heart failure
Hypertension
Mineralocorticoid receptor blockers
Journal
Current hypertension reports
ISSN: 1534-3111
Titre abrégé: Curr Hypertens Rep
Pays: United States
ID NLM: 100888982
Informations de publication
Date de publication:
29 02 2020
29 02 2020
Historique:
entrez:
2
3
2020
pubmed:
3
3
2020
medline:
20
9
2020
Statut:
epublish
Résumé
Recently, nonsteroidal mineralocorticoid receptor (MR) antagonists (MRAs), which have been proposed to be called MR blockers (MRBs), have become available for clinical use, but their clinical role is unknown. We reviewed the clinical roles of MRAs and MRBs based on previous knowledge and as demonstrated in representative clinical trials. Steroidal MRAs, such as spironolactone and eplerenone, inhibit the action of aldosterone and cortisol in MRs expressed in several organs and cell types, and accumulating clinical studies have revealed that they exert hypotensive and cardiorenal protective effects. Recently, MRBs, including finerenone and esaxerenone, have been developed and are expected to lower the risk of hyperkalemia, which is common when steroidal MRAs are used. Although the differences between MRAs and MRBs in clinical practice have not yet been established, further studies in this field are expected to broaden our understanding. MRBs exert antihypertensive and cardiorenal protective effects, and their potency is thought to be far superior to that of MRAs, because MRBs have both strong MR inhibitory action and high selectivity. Thus, MRBs could be a promising agent for the treatment of hypertension and cardiorenal, cerebral, and metabolic disorders.
Identifiants
pubmed: 32114686
doi: 10.1007/s11906-020-1023-y
pii: 10.1007/s11906-020-1023-y
doi:
Substances chimiques
Mineralocorticoid Receptor Antagonists
0
Receptors, Mineralocorticoid
0
Spironolactone
27O7W4T232
Eplerenone
6995V82D0B
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
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