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Effect of dermatan sulphate on a C57-mouse model of pulmonary fibrosis
OBJECTIVE: To test the antifibrotic effect of dermatan sulphate in a bleomycin-induced mouse model of pulmonary fibrosis. METHODS: C57 mice were randomly divided into four experimental groups: saline-treated control group, bleomycin-induced fibrosis group, prednisolone acetate group and dermatan sul...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567691/ https://www.ncbi.nlm.nih.gov/pubmed/31006321 http://dx.doi.org/10.1177/0300060519842048 |
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author | Xu, Jianfeng Li, Wei Xu, Shufen Gao, Weiyang Yu, Zhenyu |
author_facet | Xu, Jianfeng Li, Wei Xu, Shufen Gao, Weiyang Yu, Zhenyu |
author_sort | Xu, Jianfeng |
collection | PubMed |
description | OBJECTIVE: To test the antifibrotic effect of dermatan sulphate in a bleomycin-induced mouse model of pulmonary fibrosis. METHODS: C57 mice were randomly divided into four experimental groups: saline-treated control group, bleomycin-induced fibrosis group, prednisolone acetate group and dermatan sulphate group. Lungs were assessed using the lung index, and the extent of interstitial fibrosis was graded using histopathological observation of haematoxylin & eosin-stained lung tissue. Lung tissue hydroxyproline levels and blood fibrinogen levels were measured using a hydroxyproline colorimetric kit and the Clauss fibrinogen assay, respectively. Tissue-type plasminogen activator (tPA) was measured using a chromogenic tPA assay kit. RESULTS: Lung index values were significantly lower in the dermatan sulphate group versus the fibrosis group. Histopathological analyses revealed that dermatan sulphate treatment ameliorated the increased inflammatory cell infiltration, and attenuated the reduction in interstitial thickening, associated with bleomycin-induced fibrosis. Hydroxyproline and fibrinogen levels were decreased in the dermatan sulphate group versus the fibrosis model group. Dermatan sulphate treatment was associated with increased tPA levels versus controls and the fibrosis group. CONCLUSIONS: Damage associated with bleomycin-induced pulmonary fibrosis was alleviated by dermatan sulphate. |
format | Online Article Text |
id | pubmed-6567691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-65676912019-06-20 Effect of dermatan sulphate on a C57-mouse model of pulmonary fibrosis Xu, Jianfeng Li, Wei Xu, Shufen Gao, Weiyang Yu, Zhenyu J Int Med Res Pre-Clinical Research Reports OBJECTIVE: To test the antifibrotic effect of dermatan sulphate in a bleomycin-induced mouse model of pulmonary fibrosis. METHODS: C57 mice were randomly divided into four experimental groups: saline-treated control group, bleomycin-induced fibrosis group, prednisolone acetate group and dermatan sulphate group. Lungs were assessed using the lung index, and the extent of interstitial fibrosis was graded using histopathological observation of haematoxylin & eosin-stained lung tissue. Lung tissue hydroxyproline levels and blood fibrinogen levels were measured using a hydroxyproline colorimetric kit and the Clauss fibrinogen assay, respectively. Tissue-type plasminogen activator (tPA) was measured using a chromogenic tPA assay kit. RESULTS: Lung index values were significantly lower in the dermatan sulphate group versus the fibrosis group. Histopathological analyses revealed that dermatan sulphate treatment ameliorated the increased inflammatory cell infiltration, and attenuated the reduction in interstitial thickening, associated with bleomycin-induced fibrosis. Hydroxyproline and fibrinogen levels were decreased in the dermatan sulphate group versus the fibrosis model group. Dermatan sulphate treatment was associated with increased tPA levels versus controls and the fibrosis group. CONCLUSIONS: Damage associated with bleomycin-induced pulmonary fibrosis was alleviated by dermatan sulphate. SAGE Publications 2019-04-21 2019-06 /pmc/articles/PMC6567691/ /pubmed/31006321 http://dx.doi.org/10.1177/0300060519842048 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Pre-Clinical Research Reports Xu, Jianfeng Li, Wei Xu, Shufen Gao, Weiyang Yu, Zhenyu Effect of dermatan sulphate on a C57-mouse model of pulmonary fibrosis |
title | Effect of dermatan sulphate on a C57-mouse model of pulmonary fibrosis |
title_full | Effect of dermatan sulphate on a C57-mouse model of pulmonary fibrosis |
title_fullStr | Effect of dermatan sulphate on a C57-mouse model of pulmonary fibrosis |
title_full_unstemmed | Effect of dermatan sulphate on a C57-mouse model of pulmonary fibrosis |
title_short | Effect of dermatan sulphate on a C57-mouse model of pulmonary fibrosis |
title_sort | effect of dermatan sulphate on a c57-mouse model of pulmonary fibrosis |
topic | Pre-Clinical Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567691/ https://www.ncbi.nlm.nih.gov/pubmed/31006321 http://dx.doi.org/10.1177/0300060519842048 |
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