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Lack of Platelet-Activating Factor Receptor Attenuates Experimental Food Allergy but Not Its Metabolic Alterations regarding Adipokine Levels

Platelet-activating factor (PAF) is known to be an important mediator of anaphylaxis. However, there is a lack of information in the literature about the role of PAF in food allergy. The aim of this work was to elucidate the participation of PAF during food allergy development and the consequent adi...

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Autores principales: Batista, Nathália Vieira, Fonseca, Roberta Cristelli, Perez, Denise, Pereira, Rafaela Vaz Sousa, de Lima Alves, Juliana, Pinho, Vanessa, Faria, Ana Maria Caetano, Cara, Denise Carmona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897668/
https://www.ncbi.nlm.nih.gov/pubmed/27314042
http://dx.doi.org/10.1155/2016/8601359
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author Batista, Nathália Vieira
Fonseca, Roberta Cristelli
Perez, Denise
Pereira, Rafaela Vaz Sousa
de Lima Alves, Juliana
Pinho, Vanessa
Faria, Ana Maria Caetano
Cara, Denise Carmona
author_facet Batista, Nathália Vieira
Fonseca, Roberta Cristelli
Perez, Denise
Pereira, Rafaela Vaz Sousa
de Lima Alves, Juliana
Pinho, Vanessa
Faria, Ana Maria Caetano
Cara, Denise Carmona
author_sort Batista, Nathália Vieira
collection PubMed
description Platelet-activating factor (PAF) is known to be an important mediator of anaphylaxis. However, there is a lack of information in the literature about the role of PAF in food allergy. The aim of this work was to elucidate the participation of PAF during food allergy development and the consequent adipose tissue inflammation along with its alterations. Our data demonstrated that, both before oral challenge and after 7 days receiving ovalbumin (OVA) diet, OVA-sensitized mice lacking the PAF receptor (PAFR) showed a decreased level of anti-OVA IgE associated with attenuated allergic markers in comparison to wild type (WT) mice. Moreover, there was less body weight and adipose tissue loss in PAFR-deficient mice. However, some features of inflamed adipose tissue presented by sensitized PAFR-deficient and WT mice after oral challenge were similar, such as a higher rate of rolling leukocytes in this tissue and lower circulating levels of adipokines (resistin and adiponectin) in comparison to nonsensitized mice. Therefore, PAF signaling through PAFR is important for the allergic response to OVA but not for the adipokine alterations caused by this inflammatory process. Our work clarifies some effects of PAF during food allergy along with its role on the metabolic consequences of this inflammatory process.
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spelling pubmed-48976682016-06-16 Lack of Platelet-Activating Factor Receptor Attenuates Experimental Food Allergy but Not Its Metabolic Alterations regarding Adipokine Levels Batista, Nathália Vieira Fonseca, Roberta Cristelli Perez, Denise Pereira, Rafaela Vaz Sousa de Lima Alves, Juliana Pinho, Vanessa Faria, Ana Maria Caetano Cara, Denise Carmona Biomed Res Int Research Article Platelet-activating factor (PAF) is known to be an important mediator of anaphylaxis. However, there is a lack of information in the literature about the role of PAF in food allergy. The aim of this work was to elucidate the participation of PAF during food allergy development and the consequent adipose tissue inflammation along with its alterations. Our data demonstrated that, both before oral challenge and after 7 days receiving ovalbumin (OVA) diet, OVA-sensitized mice lacking the PAF receptor (PAFR) showed a decreased level of anti-OVA IgE associated with attenuated allergic markers in comparison to wild type (WT) mice. Moreover, there was less body weight and adipose tissue loss in PAFR-deficient mice. However, some features of inflamed adipose tissue presented by sensitized PAFR-deficient and WT mice after oral challenge were similar, such as a higher rate of rolling leukocytes in this tissue and lower circulating levels of adipokines (resistin and adiponectin) in comparison to nonsensitized mice. Therefore, PAF signaling through PAFR is important for the allergic response to OVA but not for the adipokine alterations caused by this inflammatory process. Our work clarifies some effects of PAF during food allergy along with its role on the metabolic consequences of this inflammatory process. Hindawi Publishing Corporation 2016 2016-05-25 /pmc/articles/PMC4897668/ /pubmed/27314042 http://dx.doi.org/10.1155/2016/8601359 Text en Copyright © 2016 Nathália Vieira Batista et al. https://creativecommons.org/licenses/by/4.0/ 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
Batista, Nathália Vieira
Fonseca, Roberta Cristelli
Perez, Denise
Pereira, Rafaela Vaz Sousa
de Lima Alves, Juliana
Pinho, Vanessa
Faria, Ana Maria Caetano
Cara, Denise Carmona
Lack of Platelet-Activating Factor Receptor Attenuates Experimental Food Allergy but Not Its Metabolic Alterations regarding Adipokine Levels
title Lack of Platelet-Activating Factor Receptor Attenuates Experimental Food Allergy but Not Its Metabolic Alterations regarding Adipokine Levels
title_full Lack of Platelet-Activating Factor Receptor Attenuates Experimental Food Allergy but Not Its Metabolic Alterations regarding Adipokine Levels
title_fullStr Lack of Platelet-Activating Factor Receptor Attenuates Experimental Food Allergy but Not Its Metabolic Alterations regarding Adipokine Levels
title_full_unstemmed Lack of Platelet-Activating Factor Receptor Attenuates Experimental Food Allergy but Not Its Metabolic Alterations regarding Adipokine Levels
title_short Lack of Platelet-Activating Factor Receptor Attenuates Experimental Food Allergy but Not Its Metabolic Alterations regarding Adipokine Levels
title_sort lack of platelet-activating factor receptor attenuates experimental food allergy but not its metabolic alterations regarding adipokine levels
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897668/
https://www.ncbi.nlm.nih.gov/pubmed/27314042
http://dx.doi.org/10.1155/2016/8601359
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