Sacubitril/valsartan treatment has differential effects in modulating diabetic kidney disease in


Journal

American journal of physiology. Renal physiology
ISSN: 1522-1466
Titre abrégé: Am J Physiol Renal Physiol
Pays: United States
ID NLM: 100901990

Informations de publication

Date de publication:
01 06 2021
Historique:
pubmed: 20 4 2021
medline: 31 7 2021
entrez: 19 4 2021
Statut: ppublish

Résumé

Although renin-angiotensin blockade has shown beneficial outcomes in patients with diabetes, renal injury progresses in most of these patients. Therefore, there remains a need for new therapeutic targets in diabetic kidney disease. Enhancement of vasoactive peptides, such as natriuretic peptides, via neprilysin inhibition, has been a new approach. A first-in-class drug, sacubitril/valsartan (Sac/Val), a combination of the angiotensin II receptor blocker Val and neprilysin inhibitor prodrug Sac, has been shown to be more effective than renin-angiotensin blockade alone in the treatment of heart failure with reduced ejection fraction. In this study, we tested the effects of Sac/Val in diabetic kidney disease. We administered Sac/Val or Val to two type 2 diabetes mouse models,

Identifiants

pubmed: 33870733
doi: 10.1152/ajprenal.00614.2020
pmc: PMC8285642
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin Receptor Antagonists 0
Biphenyl Compounds 0
Drug Combinations 0
Valsartan 80M03YXJ7I
sacubitril and valsartan sodium hydrate drug combination WB8FT61183

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

F1133-F1151

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK116567
Pays : United States
Organisme : NCATS NIH HHS
ID : TL1 TR001431
Pays : United States
Organisme : HHS | NIH | National Center for Advancing Translational Sciences (NCATS)
ID : TL1TR001431
Organisme : HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ID : 5R01DK116567

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Auteurs

Komuraiah Myakala (K)

Department of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, District of Columbia.

Bryce A Jones (BA)

Department of Pharmacology and Physiology, Georgetown University, Washington, District of Columbia.

Xiaoxin X Wang (XX)

Department of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, District of Columbia.

Moshe Levi (M)

Department of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, District of Columbia.

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Classifications MeSH