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The effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline-induced right ventricular failure

PURPOSE: Pulmonary arterial hypertension (PAH) leads to right ventricular failure (RVF) as well as an increase in pulmonary vascular resistance. Our purpose was to study the effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline (MCT)-induced RVF. METHODS: The rats were...

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Autores principales: Bae, Hyun Kyung, Lee, Hyeryon, Kim, Kwan Chang, Hong, Young Mi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958704/
https://www.ncbi.nlm.nih.gov/pubmed/27462355
http://dx.doi.org/10.3345/kjp.2016.59.6.262
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author Bae, Hyun Kyung
Lee, Hyeryon
Kim, Kwan Chang
Hong, Young Mi
author_facet Bae, Hyun Kyung
Lee, Hyeryon
Kim, Kwan Chang
Hong, Young Mi
author_sort Bae, Hyun Kyung
collection PubMed
description PURPOSE: Pulmonary arterial hypertension (PAH) leads to right ventricular failure (RVF) as well as an increase in pulmonary vascular resistance. Our purpose was to study the effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline (MCT)-induced RVF. METHODS: The rats were distributed randomly into 3 groups. The control (C) group, the monocrotaline (M) group (MCT 60 mg/kg) and the sildenafil (S) group (MCT 60 mg/kg+ sildenafil 30 mg/kg/day for 28 days). Masson Trichrome staining was used for heart tissues. Western blot analysis and immunohistochemical staining were performed. RESULTS: The mean right ventricular pressure (RVP) was significantly lower in the S group at weeks 1, 2, and 4. The number of intra-acinar arteries and the medial wall thickness of the pulmonary arterioles significantly lessened in the S group at week 4. The collagen content also decreased in heart tissues in the S group at week 4. Protein expression levels of B-cell lymphoma-2 (Bcl-2)-associated X, caspase-3, Bcl-2, interleukin (IL)-6, matrix metalloproteinase (MMP)-2, endothelial nitric oxide synthase (eNOS), endothelin (ET)-1 and ET receptor A (ERA) in lung tissues greatly decreased in the S group at week 4 according to immunohistochemical staining. According to Western blotting, protein expression levels of troponin I, brain natriuretic peptide, caspase-3, Bcl-2, tumor necrosis factor-α, IL-6, MMP-2, eNOS, ET-1, and ERA in heart tissues greatly diminished in the S group at week 4. CONCLUSION: Sildenafil alleviated right ventricular hypertrophy and mean RVP. These data suggest that sildenafil improves right ventricular function.
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spelling pubmed-49587042016-07-26 The effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline-induced right ventricular failure Bae, Hyun Kyung Lee, Hyeryon Kim, Kwan Chang Hong, Young Mi Korean J Pediatr Original Article PURPOSE: Pulmonary arterial hypertension (PAH) leads to right ventricular failure (RVF) as well as an increase in pulmonary vascular resistance. Our purpose was to study the effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline (MCT)-induced RVF. METHODS: The rats were distributed randomly into 3 groups. The control (C) group, the monocrotaline (M) group (MCT 60 mg/kg) and the sildenafil (S) group (MCT 60 mg/kg+ sildenafil 30 mg/kg/day for 28 days). Masson Trichrome staining was used for heart tissues. Western blot analysis and immunohistochemical staining were performed. RESULTS: The mean right ventricular pressure (RVP) was significantly lower in the S group at weeks 1, 2, and 4. The number of intra-acinar arteries and the medial wall thickness of the pulmonary arterioles significantly lessened in the S group at week 4. The collagen content also decreased in heart tissues in the S group at week 4. Protein expression levels of B-cell lymphoma-2 (Bcl-2)-associated X, caspase-3, Bcl-2, interleukin (IL)-6, matrix metalloproteinase (MMP)-2, endothelial nitric oxide synthase (eNOS), endothelin (ET)-1 and ET receptor A (ERA) in lung tissues greatly decreased in the S group at week 4 according to immunohistochemical staining. According to Western blotting, protein expression levels of troponin I, brain natriuretic peptide, caspase-3, Bcl-2, tumor necrosis factor-α, IL-6, MMP-2, eNOS, ET-1, and ERA in heart tissues greatly diminished in the S group at week 4. CONCLUSION: Sildenafil alleviated right ventricular hypertrophy and mean RVP. These data suggest that sildenafil improves right ventricular function. The Korean Pediatric Society 2016-06 2016-06-30 /pmc/articles/PMC4958704/ /pubmed/27462355 http://dx.doi.org/10.3345/kjp.2016.59.6.262 Text en Copyright © 2016 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Bae, Hyun Kyung
Lee, Hyeryon
Kim, Kwan Chang
Hong, Young Mi
The effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline-induced right ventricular failure
title The effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline-induced right ventricular failure
title_full The effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline-induced right ventricular failure
title_fullStr The effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline-induced right ventricular failure
title_full_unstemmed The effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline-induced right ventricular failure
title_short The effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline-induced right ventricular failure
title_sort effect of sildenafil on right ventricular remodeling in a rat model of monocrotaline-induced right ventricular failure
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958704/
https://www.ncbi.nlm.nih.gov/pubmed/27462355
http://dx.doi.org/10.3345/kjp.2016.59.6.262
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