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Coadministration of Atorvastatin and Amiodarone Increases the Risk of Pulmonary Fibrosis in Rats
OBJECTIVE: The purpose of this study was to evaluate the effect of atorvastatin administration on amiodarone-induced pulmonary fibrosis in rats. MATERIALS AND METHODS: Thirty-six male Wistar rats were randomly divided into 4 groups. The control group (CTL) received distilled water (0.3 ml intratrach...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588350/ https://www.ncbi.nlm.nih.gov/pubmed/26544718 http://dx.doi.org/10.1159/000442202 |
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author | Nasri, Hamid-Reza Joukar, Siyavash Kheradmand, Hamid Poursalehi, Hamid-Reza Dabiri, Shahriar |
author_facet | Nasri, Hamid-Reza Joukar, Siyavash Kheradmand, Hamid Poursalehi, Hamid-Reza Dabiri, Shahriar |
author_sort | Nasri, Hamid-Reza |
collection | PubMed |
description | OBJECTIVE: The purpose of this study was to evaluate the effect of atorvastatin administration on amiodarone-induced pulmonary fibrosis in rats. MATERIALS AND METHODS: Thirty-six male Wistar rats were randomly divided into 4 groups. The control group (CTL) received distilled water (0.3 ml intratracheally on days 0 and 2 and 0.5 ml orally from day 0 for 3 weeks). The atorvastatin group (AT), in addition to intratracheal distilled water, received 1 mg/kg of atorvastatin orally from day 0 for 3 weeks. The amiodarone group (AMI) received 2 intratracheal instillations of amiodarone (6.25 mg/kg in 0.3 ml of water) on days 0 and 2 and 0.5 ml of distilled water (like the CTL). The amiodarone plus atorvastatin group (AMI + AT) received both these drugs (same doses and methods as for the AMI and AT). After 28 days, the rate of lung fibrosis was estimated according to pathological criteria of lung sections and measurements of hydroxyproline in pieces of left lung tissue. RESULTS: The lung hydroxyproline content was higher in the treated groups (CTL: 0.35 ± 0.017, AT: 0.38 ± 0.012, AMI: 0.375 ± 0.018 and AMI + AT: 0.38 ± 0.012 unit/mg protein), but did not reach significance when compared with the CTL (p = 0.56). Amiodarone administration significantly increased the score of pulmonary fibrosis (0.5) in comparison with the AT (0.125) and CTL (0) (p < 0.5). The combination of amiodarone and atorvastatin exacerbated the pulmonary fibrosis (1.5; p < 0.01) compared to the AMI (0.5; p < 0.001), AT (0.125) and CTL (0). CONCLUSION: In this study, the concomitant administration of amiodarone and atorvastatin increased pulmonary fibrosis in rats. |
format | Online Article Text |
id | pubmed-5588350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-55883502017-11-01 Coadministration of Atorvastatin and Amiodarone Increases the Risk of Pulmonary Fibrosis in Rats Nasri, Hamid-Reza Joukar, Siyavash Kheradmand, Hamid Poursalehi, Hamid-Reza Dabiri, Shahriar Med Princ Pract Original Paper OBJECTIVE: The purpose of this study was to evaluate the effect of atorvastatin administration on amiodarone-induced pulmonary fibrosis in rats. MATERIALS AND METHODS: Thirty-six male Wistar rats were randomly divided into 4 groups. The control group (CTL) received distilled water (0.3 ml intratracheally on days 0 and 2 and 0.5 ml orally from day 0 for 3 weeks). The atorvastatin group (AT), in addition to intratracheal distilled water, received 1 mg/kg of atorvastatin orally from day 0 for 3 weeks. The amiodarone group (AMI) received 2 intratracheal instillations of amiodarone (6.25 mg/kg in 0.3 ml of water) on days 0 and 2 and 0.5 ml of distilled water (like the CTL). The amiodarone plus atorvastatin group (AMI + AT) received both these drugs (same doses and methods as for the AMI and AT). After 28 days, the rate of lung fibrosis was estimated according to pathological criteria of lung sections and measurements of hydroxyproline in pieces of left lung tissue. RESULTS: The lung hydroxyproline content was higher in the treated groups (CTL: 0.35 ± 0.017, AT: 0.38 ± 0.012, AMI: 0.375 ± 0.018 and AMI + AT: 0.38 ± 0.012 unit/mg protein), but did not reach significance when compared with the CTL (p = 0.56). Amiodarone administration significantly increased the score of pulmonary fibrosis (0.5) in comparison with the AT (0.125) and CTL (0) (p < 0.5). The combination of amiodarone and atorvastatin exacerbated the pulmonary fibrosis (1.5; p < 0.01) compared to the AMI (0.5; p < 0.001), AT (0.125) and CTL (0). CONCLUSION: In this study, the concomitant administration of amiodarone and atorvastatin increased pulmonary fibrosis in rats. S. Karger AG 2016-02 2015-11-06 /pmc/articles/PMC5588350/ /pubmed/26544718 http://dx.doi.org/10.1159/000442202 Text en Copyright © 2015 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Distribution permitted for non-commercial purposes only. |
spellingShingle | Original Paper Nasri, Hamid-Reza Joukar, Siyavash Kheradmand, Hamid Poursalehi, Hamid-Reza Dabiri, Shahriar Coadministration of Atorvastatin and Amiodarone Increases the Risk of Pulmonary Fibrosis in Rats |
title | Coadministration of Atorvastatin and Amiodarone Increases the Risk of Pulmonary Fibrosis in Rats |
title_full | Coadministration of Atorvastatin and Amiodarone Increases the Risk of Pulmonary Fibrosis in Rats |
title_fullStr | Coadministration of Atorvastatin and Amiodarone Increases the Risk of Pulmonary Fibrosis in Rats |
title_full_unstemmed | Coadministration of Atorvastatin and Amiodarone Increases the Risk of Pulmonary Fibrosis in Rats |
title_short | Coadministration of Atorvastatin and Amiodarone Increases the Risk of Pulmonary Fibrosis in Rats |
title_sort | coadministration of atorvastatin and amiodarone increases the risk of pulmonary fibrosis in rats |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588350/ https://www.ncbi.nlm.nih.gov/pubmed/26544718 http://dx.doi.org/10.1159/000442202 |
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