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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...

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Autores principales: Niu, Fangfang, Li, Huafei, Xu, Xiaotao, Sun, Lingling, Gan, Ning, Wang, Aizhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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