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Effects of Anacardic Acid Monoene on the Respiratory System of Mice Submitted to Acute Respiratory Distress Syndrome
The acute respiratory distress syndrome caused by viral pathogens is a worldwide public health emergency. It is suggested that patients with this condition should be screened using therapies that address the need to prevent mortality. Anacardic acids found in Anacardium species have biological activ...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092365/ https://www.ncbi.nlm.nih.gov/pubmed/33967357 http://dx.doi.org/10.1007/s43450-021-00151-8 |
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author | de Lima Gondim, Fladimir Ferreira, Ruth Mesquita Nogueira, Tiago Rocha Serra, Daniel Silveira de Sousa Rios, Maria Alexandra Pimenta, Antônia Torres Ávila Cavalcante, Francisco Sales Ávila |
author_facet | de Lima Gondim, Fladimir Ferreira, Ruth Mesquita Nogueira, Tiago Rocha Serra, Daniel Silveira de Sousa Rios, Maria Alexandra Pimenta, Antônia Torres Ávila Cavalcante, Francisco Sales Ávila |
author_sort | de Lima Gondim, Fladimir |
collection | PubMed |
description | The acute respiratory distress syndrome caused by viral pathogens is a worldwide public health emergency. It is suggested that patients with this condition should be screened using therapies that address the need to prevent mortality. Anacardic acids found in Anacardium species have biological activities related to the antioxidant capacity of their double bonds in the lateral alkyl chain. The present study seeks to investigate the effects of anacardic acid monoene on acute respiratory distress syndrome caused by lipopolysaccharides. Experiments were carried out on mice divided into three groups: control group, acute respiratory distress-induced group, and anacardic acid monoene pretreated group, subsequently, induced to acute respiratory distress by lipopolysaccharides. Results showed that anacardic acid moeno was able to prevent changes in lung function and preserve its mechanical properties from containing inflammatory cell infiltrate, collapse of alveoli, and decreased airway resistance, suggesting that this compound may be effective in preventing the acute respiratory distress syndrome caused by viral pathogens. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43450-021-00151-8. |
format | Online Article Text |
id | pubmed-8092365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-80923652021-05-05 Effects of Anacardic Acid Monoene on the Respiratory System of Mice Submitted to Acute Respiratory Distress Syndrome de Lima Gondim, Fladimir Ferreira, Ruth Mesquita Nogueira, Tiago Rocha Serra, Daniel Silveira de Sousa Rios, Maria Alexandra Pimenta, Antônia Torres Ávila Cavalcante, Francisco Sales Ávila Rev Bras Farmacogn Original Article The acute respiratory distress syndrome caused by viral pathogens is a worldwide public health emergency. It is suggested that patients with this condition should be screened using therapies that address the need to prevent mortality. Anacardic acids found in Anacardium species have biological activities related to the antioxidant capacity of their double bonds in the lateral alkyl chain. The present study seeks to investigate the effects of anacardic acid monoene on acute respiratory distress syndrome caused by lipopolysaccharides. Experiments were carried out on mice divided into three groups: control group, acute respiratory distress-induced group, and anacardic acid monoene pretreated group, subsequently, induced to acute respiratory distress by lipopolysaccharides. Results showed that anacardic acid moeno was able to prevent changes in lung function and preserve its mechanical properties from containing inflammatory cell infiltrate, collapse of alveoli, and decreased airway resistance, suggesting that this compound may be effective in preventing the acute respiratory distress syndrome caused by viral pathogens. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43450-021-00151-8. Springer International Publishing 2021-05-03 2021 /pmc/articles/PMC8092365/ /pubmed/33967357 http://dx.doi.org/10.1007/s43450-021-00151-8 Text en © Sociedade Brasileira de Farmacognosia 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article de Lima Gondim, Fladimir Ferreira, Ruth Mesquita Nogueira, Tiago Rocha Serra, Daniel Silveira de Sousa Rios, Maria Alexandra Pimenta, Antônia Torres Ávila Cavalcante, Francisco Sales Ávila Effects of Anacardic Acid Monoene on the Respiratory System of Mice Submitted to Acute Respiratory Distress Syndrome |
title | Effects of Anacardic Acid Monoene on the Respiratory System of Mice Submitted to Acute Respiratory Distress Syndrome |
title_full | Effects of Anacardic Acid Monoene on the Respiratory System of Mice Submitted to Acute Respiratory Distress Syndrome |
title_fullStr | Effects of Anacardic Acid Monoene on the Respiratory System of Mice Submitted to Acute Respiratory Distress Syndrome |
title_full_unstemmed | Effects of Anacardic Acid Monoene on the Respiratory System of Mice Submitted to Acute Respiratory Distress Syndrome |
title_short | Effects of Anacardic Acid Monoene on the Respiratory System of Mice Submitted to Acute Respiratory Distress Syndrome |
title_sort | effects of anacardic acid monoene on the respiratory system of mice submitted to acute respiratory distress syndrome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092365/ https://www.ncbi.nlm.nih.gov/pubmed/33967357 http://dx.doi.org/10.1007/s43450-021-00151-8 |
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