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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
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.
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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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