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Determination of the effects of pulmonary arterial hypertension and therapy on the cardiovascular system of rats by impedance cardiography
AIM: To evaluate the effects of bosentan, sildenafil, and combined therapy on the cardiovascular system using impedance cardiography (ICG) in rats with monocrotaline (MCT)-induced pulmonary arterial hypertension (PAH). METHODS: Seventy male Wistar-albino rats were randomized into five groups. A sing...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Croatian Medical Schools
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228293/ https://www.ncbi.nlm.nih.gov/pubmed/25358882 http://dx.doi.org/10.3325/cmj.2014.55.498 |
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author | Buyukakilli, Belgin Gurgul, Serkan Cıtırık, Derya Hallioglu, Olgu Ozeren, Murat Tasdelen, Bahar |
author_facet | Buyukakilli, Belgin Gurgul, Serkan Cıtırık, Derya Hallioglu, Olgu Ozeren, Murat Tasdelen, Bahar |
author_sort | Buyukakilli, Belgin |
collection | PubMed |
description | AIM: To evaluate the effects of bosentan, sildenafil, and combined therapy on the cardiovascular system using impedance cardiography (ICG) in rats with monocrotaline (MCT)-induced pulmonary arterial hypertension (PAH). METHODS: Seventy male Wistar-albino rats were randomized into five groups. A single dose of MCT was given to all rats, except to the control group. After 4 weeks, bosentan, sildenafil, and combined treatment was started and lasted for 3 weeks. The last group that developed PAH did not receive any medication. Echocardiographic evaluation was performed to determine the PAH development. Thoracic fluid content index (TFCI), stroke volume index (SI), heart rate (HR), cardiac index (CI), and myocardial contractility index (IC) were determined. All procedures were performed at the baseline and after 4 and 7 weeks. RESULTS: Echocardiographic parameters showed that the all MCT-injected rats developed PAH. There were no significant inter- and intra-group differences in TFCI, SI, and IC (P > 0.05), but at the 7th week, CI value in the sildenafil-treated PAH rats was significantly higher than in other groups and HR of PAH rats with combined therapy was significantly lower than in other groups. CONCLUSION: PAH did not have an effect on LV function of rats, or if it did, the effect was compensated by physiological processes. Also, sildenafil treatment deteriorated the LV cardiac index. |
format | Online Article Text |
id | pubmed-4228293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Croatian Medical Schools |
record_format | MEDLINE/PubMed |
spelling | pubmed-42282932014-11-17 Determination of the effects of pulmonary arterial hypertension and therapy on the cardiovascular system of rats by impedance cardiography Buyukakilli, Belgin Gurgul, Serkan Cıtırık, Derya Hallioglu, Olgu Ozeren, Murat Tasdelen, Bahar Croat Med J Basic Science AIM: To evaluate the effects of bosentan, sildenafil, and combined therapy on the cardiovascular system using impedance cardiography (ICG) in rats with monocrotaline (MCT)-induced pulmonary arterial hypertension (PAH). METHODS: Seventy male Wistar-albino rats were randomized into five groups. A single dose of MCT was given to all rats, except to the control group. After 4 weeks, bosentan, sildenafil, and combined treatment was started and lasted for 3 weeks. The last group that developed PAH did not receive any medication. Echocardiographic evaluation was performed to determine the PAH development. Thoracic fluid content index (TFCI), stroke volume index (SI), heart rate (HR), cardiac index (CI), and myocardial contractility index (IC) were determined. All procedures were performed at the baseline and after 4 and 7 weeks. RESULTS: Echocardiographic parameters showed that the all MCT-injected rats developed PAH. There were no significant inter- and intra-group differences in TFCI, SI, and IC (P > 0.05), but at the 7th week, CI value in the sildenafil-treated PAH rats was significantly higher than in other groups and HR of PAH rats with combined therapy was significantly lower than in other groups. CONCLUSION: PAH did not have an effect on LV function of rats, or if it did, the effect was compensated by physiological processes. Also, sildenafil treatment deteriorated the LV cardiac index. Croatian Medical Schools 2014-10 /pmc/articles/PMC4228293/ /pubmed/25358882 http://dx.doi.org/10.3325/cmj.2014.55.498 Text en Copyright © 2014 by the Croatian Medical Journal. All rights reserved. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Basic Science Buyukakilli, Belgin Gurgul, Serkan Cıtırık, Derya Hallioglu, Olgu Ozeren, Murat Tasdelen, Bahar Determination of the effects of pulmonary arterial hypertension and therapy on the cardiovascular system of rats by impedance cardiography |
title | Determination of the effects of pulmonary arterial hypertension and therapy on the cardiovascular system of rats by impedance cardiography |
title_full | Determination of the effects of pulmonary arterial hypertension and therapy on the cardiovascular system of rats by impedance cardiography |
title_fullStr | Determination of the effects of pulmonary arterial hypertension and therapy on the cardiovascular system of rats by impedance cardiography |
title_full_unstemmed | Determination of the effects of pulmonary arterial hypertension and therapy on the cardiovascular system of rats by impedance cardiography |
title_short | Determination of the effects of pulmonary arterial hypertension and therapy on the cardiovascular system of rats by impedance cardiography |
title_sort | determination of the effects of pulmonary arterial hypertension and therapy on the cardiovascular system of rats by impedance cardiography |
topic | Basic Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228293/ https://www.ncbi.nlm.nih.gov/pubmed/25358882 http://dx.doi.org/10.3325/cmj.2014.55.498 |
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