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Predictive Criteria to Study the Pathogenesis of Malaria-Associated ALI/ARDS in Mice
Malaria-associated acute lung injury/acute respiratory distress syndrome (ALI/ARDS) often results in morbidity and mortality. Murine models to study malaria-associated ALI/ARDS have been described; we still lack a method of distinguishing which mice will develop ALI/ARDS before death. This work aime...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4167651/ https://www.ncbi.nlm.nih.gov/pubmed/25276057 http://dx.doi.org/10.1155/2014/872464 |
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author | Ortolan, Luana S. Sercundes, Michelle K. Barboza, Renato Debone, Daniela Murillo, Oscar Hagen, Stefano C. F. Russo, Momtchilo D' Império Lima, Maria Regina Alvarez, José M. Amaku, Marcos Marinho, Claudio R. F. Epiphanio, Sabrina |
author_facet | Ortolan, Luana S. Sercundes, Michelle K. Barboza, Renato Debone, Daniela Murillo, Oscar Hagen, Stefano C. F. Russo, Momtchilo D' Império Lima, Maria Regina Alvarez, José M. Amaku, Marcos Marinho, Claudio R. F. Epiphanio, Sabrina |
author_sort | Ortolan, Luana S. |
collection | PubMed |
description | Malaria-associated acute lung injury/acute respiratory distress syndrome (ALI/ARDS) often results in morbidity and mortality. Murine models to study malaria-associated ALI/ARDS have been described; we still lack a method of distinguishing which mice will develop ALI/ARDS before death. This work aimed to characterize malaria-associated ALI/ARDS in a murine model and to demonstrate the first method to predict whether mice are suffering from ALI/ARDS before death. DBA/2 mice infected with Plasmodium berghei ANKA developing ALI/ARDS or hyperparasitemia (HP) were compared using histopathology, PaO(2) measurement, pulmonary X-ray, breathing capacity, lung permeability, and serum vascular endothelial growth factor (VEGF) levels according to either the day of death or the suggested predictive criteria. We proposed a model to predict malaria-associated ALI/ARDS using breathing patterns (enhanced pause and frequency respiration) and parasitemia as predictive criteria from mice whose cause of death was known to retrospectively diagnose the sacrificed mice as likely to die of ALI/ARDS as early as 7 days after infection. Using this method, we showed increased VEGF levels and increased lung permeability in mice predicted to die of ALI/ARDS. This proposed method for accurately identifying mice suffering from ALI/ARDS before death will enable the use of this model to study the pathogenesis of this disease. |
format | Online Article Text |
id | pubmed-4167651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-41676512014-09-28 Predictive Criteria to Study the Pathogenesis of Malaria-Associated ALI/ARDS in Mice Ortolan, Luana S. Sercundes, Michelle K. Barboza, Renato Debone, Daniela Murillo, Oscar Hagen, Stefano C. F. Russo, Momtchilo D' Império Lima, Maria Regina Alvarez, José M. Amaku, Marcos Marinho, Claudio R. F. Epiphanio, Sabrina Mediators Inflamm Research Article Malaria-associated acute lung injury/acute respiratory distress syndrome (ALI/ARDS) often results in morbidity and mortality. Murine models to study malaria-associated ALI/ARDS have been described; we still lack a method of distinguishing which mice will develop ALI/ARDS before death. This work aimed to characterize malaria-associated ALI/ARDS in a murine model and to demonstrate the first method to predict whether mice are suffering from ALI/ARDS before death. DBA/2 mice infected with Plasmodium berghei ANKA developing ALI/ARDS or hyperparasitemia (HP) were compared using histopathology, PaO(2) measurement, pulmonary X-ray, breathing capacity, lung permeability, and serum vascular endothelial growth factor (VEGF) levels according to either the day of death or the suggested predictive criteria. We proposed a model to predict malaria-associated ALI/ARDS using breathing patterns (enhanced pause and frequency respiration) and parasitemia as predictive criteria from mice whose cause of death was known to retrospectively diagnose the sacrificed mice as likely to die of ALI/ARDS as early as 7 days after infection. Using this method, we showed increased VEGF levels and increased lung permeability in mice predicted to die of ALI/ARDS. This proposed method for accurately identifying mice suffering from ALI/ARDS before death will enable the use of this model to study the pathogenesis of this disease. Hindawi Publishing Corporation 2014 2014-09-02 /pmc/articles/PMC4167651/ /pubmed/25276057 http://dx.doi.org/10.1155/2014/872464 Text en Copyright © 2014 Luana S. Ortolan 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 Ortolan, Luana S. Sercundes, Michelle K. Barboza, Renato Debone, Daniela Murillo, Oscar Hagen, Stefano C. F. Russo, Momtchilo D' Império Lima, Maria Regina Alvarez, José M. Amaku, Marcos Marinho, Claudio R. F. Epiphanio, Sabrina Predictive Criteria to Study the Pathogenesis of Malaria-Associated ALI/ARDS in Mice |
title | Predictive Criteria to Study the Pathogenesis of Malaria-Associated ALI/ARDS in Mice |
title_full | Predictive Criteria to Study the Pathogenesis of Malaria-Associated ALI/ARDS in Mice |
title_fullStr | Predictive Criteria to Study the Pathogenesis of Malaria-Associated ALI/ARDS in Mice |
title_full_unstemmed | Predictive Criteria to Study the Pathogenesis of Malaria-Associated ALI/ARDS in Mice |
title_short | Predictive Criteria to Study the Pathogenesis of Malaria-Associated ALI/ARDS in Mice |
title_sort | predictive criteria to study the pathogenesis of malaria-associated ali/ards in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4167651/ https://www.ncbi.nlm.nih.gov/pubmed/25276057 http://dx.doi.org/10.1155/2014/872464 |
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