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Ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome
Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a life‐threatening disease with a high mortality rate, which was a common complication of fat embolism syndrome (FES). Ursodeoxycholic acid (UDCA) has been reported to exert potent anti‐inflammatory effects under various condition...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754031/ https://www.ncbi.nlm.nih.gov/pubmed/33145933 http://dx.doi.org/10.1111/jcmm.15985 |
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author | Niu, Fangfang Li, Huafei Xu, Xiaotao Sun, Lingling Gan, Ning Wang, Aizhong |
author_facet | Niu, Fangfang Li, Huafei Xu, Xiaotao Sun, Lingling Gan, Ning Wang, Aizhong |
author_sort | Niu, Fangfang |
collection | PubMed |
description | Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a life‐threatening disease with a high mortality rate, which was a common complication of fat embolism syndrome (FES). Ursodeoxycholic acid (UDCA) has been reported to exert potent anti‐inflammatory effects under various conditions. In vivo, perinephric fat was injected via tail vein to establish a rat FES model, the anti‐inflammatory effects of UDCA on FES‐induced lung injury were investigated through histological examination, ELISA, qRT‐PCR, Western blot and immunofluorescence. In vitro, human lung microvascular endothelial cells (HPMECs) were employed to understand the protective effects of UDCA. The extent of ALI/ARDS was evaluated and validated by reduced PaO(2)/FiO(2) ratios, increased lung wet/dry (W/D) ratios and impaired alveolar‐capillary barrier, up‐regulation of ALI‐related proteins in lung tissues (including myeloperoxidase [MPO], vascular cell adhesion molecule 1 [VCAM‐1], intercellular cell adhesion molecule‐1 [ICAM‐1]), elevated protein concentration and increased proinflammatory cytokines levels (TNF‐α and IL‐1β) in bronchoalveolar lavage fluid (BALF). Pre‐treatment with UDCA remarkably alleviated these pathologic and biochemical changes of FES‐induced ALI/ARDS; our data demonstrated that pre‐treatment with UDCA attenuated the pathologic and biochemical changes of FES‐induced ARDS, which provided a possible preventive therapy for lung injury caused by FES. |
format | Online Article Text |
id | pubmed-7754031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77540312020-12-23 Ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome Niu, Fangfang Li, Huafei Xu, Xiaotao Sun, Lingling Gan, Ning Wang, Aizhong J Cell Mol Med Short Communications Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a life‐threatening disease with a high mortality rate, which was a common complication of fat embolism syndrome (FES). Ursodeoxycholic acid (UDCA) has been reported to exert potent anti‐inflammatory effects under various conditions. In vivo, perinephric fat was injected via tail vein to establish a rat FES model, the anti‐inflammatory effects of UDCA on FES‐induced lung injury were investigated through histological examination, ELISA, qRT‐PCR, Western blot and immunofluorescence. In vitro, human lung microvascular endothelial cells (HPMECs) were employed to understand the protective effects of UDCA. The extent of ALI/ARDS was evaluated and validated by reduced PaO(2)/FiO(2) ratios, increased lung wet/dry (W/D) ratios and impaired alveolar‐capillary barrier, up‐regulation of ALI‐related proteins in lung tissues (including myeloperoxidase [MPO], vascular cell adhesion molecule 1 [VCAM‐1], intercellular cell adhesion molecule‐1 [ICAM‐1]), elevated protein concentration and increased proinflammatory cytokines levels (TNF‐α and IL‐1β) in bronchoalveolar lavage fluid (BALF). Pre‐treatment with UDCA remarkably alleviated these pathologic and biochemical changes of FES‐induced ALI/ARDS; our data demonstrated that pre‐treatment with UDCA attenuated the pathologic and biochemical changes of FES‐induced ARDS, which provided a possible preventive therapy for lung injury caused by FES. John Wiley and Sons Inc. 2020-11-04 2020-12 /pmc/articles/PMC7754031/ /pubmed/33145933 http://dx.doi.org/10.1111/jcmm.15985 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communications Niu, Fangfang Li, Huafei Xu, Xiaotao Sun, Lingling Gan, Ning Wang, Aizhong Ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome |
title | Ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome |
title_full | Ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome |
title_fullStr | Ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome |
title_full_unstemmed | Ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome |
title_short | Ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome |
title_sort | ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754031/ https://www.ncbi.nlm.nih.gov/pubmed/33145933 http://dx.doi.org/10.1111/jcmm.15985 |
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