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Prevention against renal damage in rats with subtotal nephrectomy by sacubitril/valsartan (LCZ696), a dual‐acting angiotensin receptor‐neprilysin inhibitor

Although patients with chronic kidney disease (CKD) are at increased risk for end‐stage renal disease and cardiovascular events, adequate drug therapies for preventing the deterioration of these conditions are still not established. This study was undertaken to evaluate a preventive effect of an ang...

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Autores principales: Ushijima, Kentaro, Ando, Hitoshi, Arakawa, Yusuke, Aizawa, Kenichi, Suzuki, Chisato, Shimada, Ken, Tsuruoka, Shu‐ichi, Fujimura, Akio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684857/
https://www.ncbi.nlm.nih.gov/pubmed/28805977
http://dx.doi.org/10.1002/prp2.336
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author Ushijima, Kentaro
Ando, Hitoshi
Arakawa, Yusuke
Aizawa, Kenichi
Suzuki, Chisato
Shimada, Ken
Tsuruoka, Shu‐ichi
Fujimura, Akio
author_facet Ushijima, Kentaro
Ando, Hitoshi
Arakawa, Yusuke
Aizawa, Kenichi
Suzuki, Chisato
Shimada, Ken
Tsuruoka, Shu‐ichi
Fujimura, Akio
author_sort Ushijima, Kentaro
collection PubMed
description Although patients with chronic kidney disease (CKD) are at increased risk for end‐stage renal disease and cardiovascular events, adequate drug therapies for preventing the deterioration of these conditions are still not established. This study was undertaken to evaluate a preventive effect of an angiotensin receptor‐neprilysin inhibitor sacubitril/valsartan (LCZ696), which is converted to sacubitril and valsartan in the body, against the progression of renal disease in rats with subtotal nephrectomy, an animal model of human CKD. Mean survival time after subtotal nephrectomy was about 100 days in Wistar rats with vehicle. LCZ696‐(30 mg/kg) and valsartan‐(15 mg/kg) prolonged the survival of these animals, and the effect of LCZ696 on survival was significantly greater than that of valsartan. Renoprotective effects of LCZ696 judged by serum creatinine and urinary protein excretions were larger than those of valsartan. Cardioprotective effects judged by cardiac left ventricular mass, fractional shortening, and fibrosis of LCZ696 and valsartan were not detected under the present condition. Thus, the renoprotective effect of LCZ696 was stronger than that of valsartan in rats with subtotal nephrectomy. This study provides the idea that, compared to valsartan, LCZ696 is more effective for the treatment of human CKD.
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spelling pubmed-56848572017-11-21 Prevention against renal damage in rats with subtotal nephrectomy by sacubitril/valsartan (LCZ696), a dual‐acting angiotensin receptor‐neprilysin inhibitor Ushijima, Kentaro Ando, Hitoshi Arakawa, Yusuke Aizawa, Kenichi Suzuki, Chisato Shimada, Ken Tsuruoka, Shu‐ichi Fujimura, Akio Pharmacol Res Perspect Original Articles Although patients with chronic kidney disease (CKD) are at increased risk for end‐stage renal disease and cardiovascular events, adequate drug therapies for preventing the deterioration of these conditions are still not established. This study was undertaken to evaluate a preventive effect of an angiotensin receptor‐neprilysin inhibitor sacubitril/valsartan (LCZ696), which is converted to sacubitril and valsartan in the body, against the progression of renal disease in rats with subtotal nephrectomy, an animal model of human CKD. Mean survival time after subtotal nephrectomy was about 100 days in Wistar rats with vehicle. LCZ696‐(30 mg/kg) and valsartan‐(15 mg/kg) prolonged the survival of these animals, and the effect of LCZ696 on survival was significantly greater than that of valsartan. Renoprotective effects of LCZ696 judged by serum creatinine and urinary protein excretions were larger than those of valsartan. Cardioprotective effects judged by cardiac left ventricular mass, fractional shortening, and fibrosis of LCZ696 and valsartan were not detected under the present condition. Thus, the renoprotective effect of LCZ696 was stronger than that of valsartan in rats with subtotal nephrectomy. This study provides the idea that, compared to valsartan, LCZ696 is more effective for the treatment of human CKD. John Wiley and Sons Inc. 2017-07-19 /pmc/articles/PMC5684857/ /pubmed/28805977 http://dx.doi.org/10.1002/prp2.336 Text en © 2017 The Authors. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Ushijima, Kentaro
Ando, Hitoshi
Arakawa, Yusuke
Aizawa, Kenichi
Suzuki, Chisato
Shimada, Ken
Tsuruoka, Shu‐ichi
Fujimura, Akio
Prevention against renal damage in rats with subtotal nephrectomy by sacubitril/valsartan (LCZ696), a dual‐acting angiotensin receptor‐neprilysin inhibitor
title Prevention against renal damage in rats with subtotal nephrectomy by sacubitril/valsartan (LCZ696), a dual‐acting angiotensin receptor‐neprilysin inhibitor
title_full Prevention against renal damage in rats with subtotal nephrectomy by sacubitril/valsartan (LCZ696), a dual‐acting angiotensin receptor‐neprilysin inhibitor
title_fullStr Prevention against renal damage in rats with subtotal nephrectomy by sacubitril/valsartan (LCZ696), a dual‐acting angiotensin receptor‐neprilysin inhibitor
title_full_unstemmed Prevention against renal damage in rats with subtotal nephrectomy by sacubitril/valsartan (LCZ696), a dual‐acting angiotensin receptor‐neprilysin inhibitor
title_short Prevention against renal damage in rats with subtotal nephrectomy by sacubitril/valsartan (LCZ696), a dual‐acting angiotensin receptor‐neprilysin inhibitor
title_sort prevention against renal damage in rats with subtotal nephrectomy by sacubitril/valsartan (lcz696), a dual‐acting angiotensin receptor‐neprilysin inhibitor
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684857/
https://www.ncbi.nlm.nih.gov/pubmed/28805977
http://dx.doi.org/10.1002/prp2.336
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