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Simvastatin impairs the induction of pulmonary fibrosis caused by a western style diet: a preliminary study

The role of an atherogenic diet in causing pulmonary fibrosis has received little attention and simvastatin has been shown to reduce pulmonary fibrosis in animal models. To determine if an atherogenic diet can induce pulmonary fibrosis and whether simvastatin treatment is beneficial by up-regulating...

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Autores principales: Kruzliak, Peter, Hare, David L, Zvonicek, Vaclav, Klimas, Jan, Zulli, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627569/
https://www.ncbi.nlm.nih.gov/pubmed/26304628
http://dx.doi.org/10.1111/jcmm.12637
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author Kruzliak, Peter
Hare, David L
Zvonicek, Vaclav
Klimas, Jan
Zulli, Anthony
author_facet Kruzliak, Peter
Hare, David L
Zvonicek, Vaclav
Klimas, Jan
Zulli, Anthony
author_sort Kruzliak, Peter
collection PubMed
description The role of an atherogenic diet in causing pulmonary fibrosis has received little attention and simvastatin has been shown to reduce pulmonary fibrosis in animal models. To determine if an atherogenic diet can induce pulmonary fibrosis and whether simvastatin treatment is beneficial by up-regulating heat shock protein 70 and 90. New Zealand white rabbits (n = 15) were divided: Group 1 (control); Group 2 (MC) received a normal rabbit diet with 1% methionine plus 0.5% cholesterol (atherogenic diet). Group 3 received the same diet as the MC group plus 5 mg/kg/day simvastatin orally (MCS). After 4 weeks, the lungs were collected and analysed. Picrosirus red staining of lung interstitial collagen content showed that the atherogenic diet increased fibrosis 2.9-fold (P < 0.05), bronchiole adventitial collagen was increased 2.3-fold (P < 0.05) and bronchiole epithelium was increased 34-fold (P < 0.05), and simvastatin treatment severely reduced this effect (P < 0.05). Western blot analysis showed that the atherogenic diet significantly reduced lung Hsp70 protein by 22% (P < 0.05) and Hsp90 protein by 18% (P < 0.05) and simvastatin treatment did not affect this result. However, aortic hyper-responsiveness to vasoconstrictors (angiotensin II and phenylephrine) were markedly reduced by simvastatin treatment. We report that an atherogenic diet stimulates pulmonary fibrosis and reduces lung Hsp70/Hsp90 protein concentration. Simvastatin impairs this by mechanisms unrelated to Hsp70/Hsp90, but possibly a reduction in angiotensin II receptor or alpha adrenergic receptor pathways. These results could have implications in idiopathic pulmonary fibrosis.
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spelling pubmed-46275692015-11-05 Simvastatin impairs the induction of pulmonary fibrosis caused by a western style diet: a preliminary study Kruzliak, Peter Hare, David L Zvonicek, Vaclav Klimas, Jan Zulli, Anthony J Cell Mol Med Original Articles The role of an atherogenic diet in causing pulmonary fibrosis has received little attention and simvastatin has been shown to reduce pulmonary fibrosis in animal models. To determine if an atherogenic diet can induce pulmonary fibrosis and whether simvastatin treatment is beneficial by up-regulating heat shock protein 70 and 90. New Zealand white rabbits (n = 15) were divided: Group 1 (control); Group 2 (MC) received a normal rabbit diet with 1% methionine plus 0.5% cholesterol (atherogenic diet). Group 3 received the same diet as the MC group plus 5 mg/kg/day simvastatin orally (MCS). After 4 weeks, the lungs were collected and analysed. Picrosirus red staining of lung interstitial collagen content showed that the atherogenic diet increased fibrosis 2.9-fold (P < 0.05), bronchiole adventitial collagen was increased 2.3-fold (P < 0.05) and bronchiole epithelium was increased 34-fold (P < 0.05), and simvastatin treatment severely reduced this effect (P < 0.05). Western blot analysis showed that the atherogenic diet significantly reduced lung Hsp70 protein by 22% (P < 0.05) and Hsp90 protein by 18% (P < 0.05) and simvastatin treatment did not affect this result. However, aortic hyper-responsiveness to vasoconstrictors (angiotensin II and phenylephrine) were markedly reduced by simvastatin treatment. We report that an atherogenic diet stimulates pulmonary fibrosis and reduces lung Hsp70/Hsp90 protein concentration. Simvastatin impairs this by mechanisms unrelated to Hsp70/Hsp90, but possibly a reduction in angiotensin II receptor or alpha adrenergic receptor pathways. These results could have implications in idiopathic pulmonary fibrosis. John Wiley & Sons, Ltd 2015-11 2015-08-25 /pmc/articles/PMC4627569/ /pubmed/26304628 http://dx.doi.org/10.1111/jcmm.12637 Text en © 2015 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Kruzliak, Peter
Hare, David L
Zvonicek, Vaclav
Klimas, Jan
Zulli, Anthony
Simvastatin impairs the induction of pulmonary fibrosis caused by a western style diet: a preliminary study
title Simvastatin impairs the induction of pulmonary fibrosis caused by a western style diet: a preliminary study
title_full Simvastatin impairs the induction of pulmonary fibrosis caused by a western style diet: a preliminary study
title_fullStr Simvastatin impairs the induction of pulmonary fibrosis caused by a western style diet: a preliminary study
title_full_unstemmed Simvastatin impairs the induction of pulmonary fibrosis caused by a western style diet: a preliminary study
title_short Simvastatin impairs the induction of pulmonary fibrosis caused by a western style diet: a preliminary study
title_sort simvastatin impairs the induction of pulmonary fibrosis caused by a western style diet: a preliminary study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627569/
https://www.ncbi.nlm.nih.gov/pubmed/26304628
http://dx.doi.org/10.1111/jcmm.12637
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