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Combination of tolvaptan and valsartan improves cardiac and renal functions in doxorubicin-induced heart failure in mice

Heart failure (HF) is often complicated by renal dysfunction. Tolvaptan and valsartan are two well-known agents for the treatment of HF. However, the role of tolvaptan/valsartan combination on HF with renal dysfunction remains unclear. To establish a mice model with HF with renal dysfunction, mice w...

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Autores principales: Yan, Fengqin, Zhu, Hong, He, Yingxia, Wu, Qinqin, Duan, Xiaoyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693770/
https://www.ncbi.nlm.nih.gov/pubmed/36373350
http://dx.doi.org/10.4081/ejh.2022.3563
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author Yan, Fengqin
Zhu, Hong
He, Yingxia
Wu, Qinqin
Duan, Xiaoyu
author_facet Yan, Fengqin
Zhu, Hong
He, Yingxia
Wu, Qinqin
Duan, Xiaoyu
author_sort Yan, Fengqin
collection PubMed
description Heart failure (HF) is often complicated by renal dysfunction. Tolvaptan and valsartan are two well-known agents for the treatment of HF. However, the role of tolvaptan/valsartan combination on HF with renal dysfunction remains unclear. To establish a mice model with HF with renal dysfunction, mice were intraperitoneally injected with doxorubicin (Dox). Echocardiogram was applied to assess the left ventricular function. Additionally, serum aldosterone (ALD) and angiotensin II (Ang II) level in mice were determined by ELISA. Meanwhile, Western blot assay was used to evaluate the expressions of B cell lymphoma-2 (Bcl-2), Bcl-2 associated X (Bax) and cleaved caspase 3 in the heart and kidney tissues of mice. In this study, we found that compared to tolvaptan or valsartan alone treatment group, tolvaptan/valsartan combination obviously improved the left ventricular ejection fraction (LVEF) and the left ventricular fractional shortening (LVFS), and reduced serum ALD and Ang II level in Dox-treated mice. Additionally, tolvaptan/valsartan combination significantly prevented the inflammation and fibrosis of heart and kidney tissues in Dox-treated mice. Meanwhile, tolvaptan/ valsartan combination notably inhibited the myocardial and renal cell apoptosis in Dox-treated mice via upregulation of Bcl-2 and downregulation of Bax and cleaved caspase 3, compared to the single drug treatment. Collectively, tolvaptan/valsartan combination could improve cardiac and renal functions, as well as prevent the fibrosis, inflammation and apoptosis of heart and kidney tissues in Dox-treated mice. Taken together, combining tolvaptan with valsartan might be a promising approach to achieve enhanced therapeutic effect for treatment of HF with renal dysfunction.
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spelling pubmed-96937702022-11-26 Combination of tolvaptan and valsartan improves cardiac and renal functions in doxorubicin-induced heart failure in mice Yan, Fengqin Zhu, Hong He, Yingxia Wu, Qinqin Duan, Xiaoyu Eur J Histochem Article Heart failure (HF) is often complicated by renal dysfunction. Tolvaptan and valsartan are two well-known agents for the treatment of HF. However, the role of tolvaptan/valsartan combination on HF with renal dysfunction remains unclear. To establish a mice model with HF with renal dysfunction, mice were intraperitoneally injected with doxorubicin (Dox). Echocardiogram was applied to assess the left ventricular function. Additionally, serum aldosterone (ALD) and angiotensin II (Ang II) level in mice were determined by ELISA. Meanwhile, Western blot assay was used to evaluate the expressions of B cell lymphoma-2 (Bcl-2), Bcl-2 associated X (Bax) and cleaved caspase 3 in the heart and kidney tissues of mice. In this study, we found that compared to tolvaptan or valsartan alone treatment group, tolvaptan/valsartan combination obviously improved the left ventricular ejection fraction (LVEF) and the left ventricular fractional shortening (LVFS), and reduced serum ALD and Ang II level in Dox-treated mice. Additionally, tolvaptan/valsartan combination significantly prevented the inflammation and fibrosis of heart and kidney tissues in Dox-treated mice. Meanwhile, tolvaptan/ valsartan combination notably inhibited the myocardial and renal cell apoptosis in Dox-treated mice via upregulation of Bcl-2 and downregulation of Bax and cleaved caspase 3, compared to the single drug treatment. Collectively, tolvaptan/valsartan combination could improve cardiac and renal functions, as well as prevent the fibrosis, inflammation and apoptosis of heart and kidney tissues in Dox-treated mice. Taken together, combining tolvaptan with valsartan might be a promising approach to achieve enhanced therapeutic effect for treatment of HF with renal dysfunction. PAGEPress Publications, Pavia, Italy 2022-11-11 /pmc/articles/PMC9693770/ /pubmed/36373350 http://dx.doi.org/10.4081/ejh.2022.3563 Text en ©Copyright: the Author(s) https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Yan, Fengqin
Zhu, Hong
He, Yingxia
Wu, Qinqin
Duan, Xiaoyu
Combination of tolvaptan and valsartan improves cardiac and renal functions in doxorubicin-induced heart failure in mice
title Combination of tolvaptan and valsartan improves cardiac and renal functions in doxorubicin-induced heart failure in mice
title_full Combination of tolvaptan and valsartan improves cardiac and renal functions in doxorubicin-induced heart failure in mice
title_fullStr Combination of tolvaptan and valsartan improves cardiac and renal functions in doxorubicin-induced heart failure in mice
title_full_unstemmed Combination of tolvaptan and valsartan improves cardiac and renal functions in doxorubicin-induced heart failure in mice
title_short Combination of tolvaptan and valsartan improves cardiac and renal functions in doxorubicin-induced heart failure in mice
title_sort combination of tolvaptan and valsartan improves cardiac and renal functions in doxorubicin-induced heart failure in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693770/
https://www.ncbi.nlm.nih.gov/pubmed/36373350
http://dx.doi.org/10.4081/ejh.2022.3563
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