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Anti-Inflammatory Effects of Ellagic Acid on Acute Lung Injury Induced by Acid in Mice
Acute lung injury (ALI) is characterized by alveolar edema and uncontrolled neutrophil migration to the lung, and no specific therapy is still available. Ellagic acid, a compound present in several fruits and medicinal plants, has shown anti-inflammatory activity in several experimental disease mode...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600201/ https://www.ncbi.nlm.nih.gov/pubmed/23533300 http://dx.doi.org/10.1155/2013/164202 |
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author | Cornélio Favarin, Daniely Martins Teixeira, Maxelle Lemos de Andrade, Ednéia de Freitas Alves, Claudiney Lazo Chica, Javier Emilio Artério Sorgi, Carlos Faccioli, Lúcia Helena Paula Rogerio, Alexandre |
author_facet | Cornélio Favarin, Daniely Martins Teixeira, Maxelle Lemos de Andrade, Ednéia de Freitas Alves, Claudiney Lazo Chica, Javier Emilio Artério Sorgi, Carlos Faccioli, Lúcia Helena Paula Rogerio, Alexandre |
author_sort | Cornélio Favarin, Daniely |
collection | PubMed |
description | Acute lung injury (ALI) is characterized by alveolar edema and uncontrolled neutrophil migration to the lung, and no specific therapy is still available. Ellagic acid, a compound present in several fruits and medicinal plants, has shown anti-inflammatory activity in several experimental disease models. We used the nonlethal acid aspiration model of ALI in mice to determine whether preventive or therapeutic administration of ellagic acid (10 mg/kg; oral route) could interfere with the development or establishment of ALI inflammation. Dexamethasone (1 mg/kg; subcutaneous route) was used as a positive control. In both preventive and therapeutic treatments, ellagic acid reduced the vascular permeability changes and neutrophil recruitment to the bronchoalveolar lavage fluid (BALF) and to lung compared to the vehicle. In addition, the ellagic acid accelerated the resolution for lung neutrophilia. Moreover, ellagic acid reduced the COX-2-induced exacerbation of inflammation. These results were similar to the dexamethasone. However, while the anti-inflammatory effects of dexamethasone treatment were due to the reduced activation of NF-κB and AP-1, the ellagic acid treatment led to reduced BALF levels of IL-6 and increased levels of IL-10. In addition, dexamethasone treatment reduced IL-1β. Together, these findings identify ellagic acid as a potential therapeutic agent for ALI-associated inflammation. |
format | Online Article Text |
id | pubmed-3600201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36002012013-03-26 Anti-Inflammatory Effects of Ellagic Acid on Acute Lung Injury Induced by Acid in Mice Cornélio Favarin, Daniely Martins Teixeira, Maxelle Lemos de Andrade, Ednéia de Freitas Alves, Claudiney Lazo Chica, Javier Emilio Artério Sorgi, Carlos Faccioli, Lúcia Helena Paula Rogerio, Alexandre Mediators Inflamm Research Article Acute lung injury (ALI) is characterized by alveolar edema and uncontrolled neutrophil migration to the lung, and no specific therapy is still available. Ellagic acid, a compound present in several fruits and medicinal plants, has shown anti-inflammatory activity in several experimental disease models. We used the nonlethal acid aspiration model of ALI in mice to determine whether preventive or therapeutic administration of ellagic acid (10 mg/kg; oral route) could interfere with the development or establishment of ALI inflammation. Dexamethasone (1 mg/kg; subcutaneous route) was used as a positive control. In both preventive and therapeutic treatments, ellagic acid reduced the vascular permeability changes and neutrophil recruitment to the bronchoalveolar lavage fluid (BALF) and to lung compared to the vehicle. In addition, the ellagic acid accelerated the resolution for lung neutrophilia. Moreover, ellagic acid reduced the COX-2-induced exacerbation of inflammation. These results were similar to the dexamethasone. However, while the anti-inflammatory effects of dexamethasone treatment were due to the reduced activation of NF-κB and AP-1, the ellagic acid treatment led to reduced BALF levels of IL-6 and increased levels of IL-10. In addition, dexamethasone treatment reduced IL-1β. Together, these findings identify ellagic acid as a potential therapeutic agent for ALI-associated inflammation. Hindawi Publishing Corporation 2013 2013-02-27 /pmc/articles/PMC3600201/ /pubmed/23533300 http://dx.doi.org/10.1155/2013/164202 Text en Copyright © 2013 Daniely Cornélio Favarin et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Cornélio Favarin, Daniely Martins Teixeira, Maxelle Lemos de Andrade, Ednéia de Freitas Alves, Claudiney Lazo Chica, Javier Emilio Artério Sorgi, Carlos Faccioli, Lúcia Helena Paula Rogerio, Alexandre Anti-Inflammatory Effects of Ellagic Acid on Acute Lung Injury Induced by Acid in Mice |
title | Anti-Inflammatory Effects of Ellagic Acid on Acute Lung Injury Induced by Acid in Mice |
title_full | Anti-Inflammatory Effects of Ellagic Acid on Acute Lung Injury Induced by Acid in Mice |
title_fullStr | Anti-Inflammatory Effects of Ellagic Acid on Acute Lung Injury Induced by Acid in Mice |
title_full_unstemmed | Anti-Inflammatory Effects of Ellagic Acid on Acute Lung Injury Induced by Acid in Mice |
title_short | Anti-Inflammatory Effects of Ellagic Acid on Acute Lung Injury Induced by Acid in Mice |
title_sort | anti-inflammatory effects of ellagic acid on acute lung injury induced by acid in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600201/ https://www.ncbi.nlm.nih.gov/pubmed/23533300 http://dx.doi.org/10.1155/2013/164202 |
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