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Oleanolic Acid Controls Allergic and Inflammatory Responses in Experimental Allergic Conjunctivitis

Pollen is the most common aeroallergen to cause seasonal conjunctivitis. The result of allergen exposure is a strong Th2-mediated response along with conjunctival mast cell degranulation and eosinophilic infiltration. Oleanolic acid (OA) is natural a triterpene that displays strong anti-inflammatory...

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Autores principales: Córdova, Claudia, Gutiérrez, Beatriz, Martínez-García, Carmen, Martín, Rubén, Gallego-Muñoz, Patricia, Hernández, Marita, Nieto, María L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974667/
https://www.ncbi.nlm.nih.gov/pubmed/24699261
http://dx.doi.org/10.1371/journal.pone.0091282
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author Córdova, Claudia
Gutiérrez, Beatriz
Martínez-García, Carmen
Martín, Rubén
Gallego-Muñoz, Patricia
Hernández, Marita
Nieto, María L.
author_facet Córdova, Claudia
Gutiérrez, Beatriz
Martínez-García, Carmen
Martín, Rubén
Gallego-Muñoz, Patricia
Hernández, Marita
Nieto, María L.
author_sort Córdova, Claudia
collection PubMed
description Pollen is the most common aeroallergen to cause seasonal conjunctivitis. The result of allergen exposure is a strong Th2-mediated response along with conjunctival mast cell degranulation and eosinophilic infiltration. Oleanolic acid (OA) is natural a triterpene that displays strong anti-inflammatory and immunomodulatory properties being an active anti-allergic molecule on hypersensitivity reaction models. However, its effect on inflammatory ocular disorders including conjunctivits, has not yet been addressed. Hence, using a Ragweed pollen (RWP)-specific allergic conjunctivitis (EAC) mouse model we study here whether OA could modify responses associated to allergic processes. We found that OA treatment restricted mast cell degranulation and infiltration of eosinophils in conjunctival tissue and decreased allergen-specific Igs levels in EAC mice. Th2-type cytokines, secreted phospholipase A(2) type-IIA (sPLA(2)-IIA), and chemokines levels were also significantly diminished in the conjunctiva and serum of OA-treated EAC mice. Moreover, OA treatment also suppressed RWP-specific T-cell proliferation. In vitro studies, on relevant cells of the allergic process, revealed that OA reduced the proliferative and migratory response, as well as the synthesis of proinflammatory mediators on EoL-1 eosinophils and RBL-2H3 mast cells exposed to allergic and/or crucial inflammatory stimuli such as RWP, sPLA(2)-IIA or eotaxin. Taken together, these findings demonstrate the beneficial activity of OA in ocular allergic processes and may provide a new intervention strategy and potential therapy for allergic diseases.
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spelling pubmed-39746672014-04-08 Oleanolic Acid Controls Allergic and Inflammatory Responses in Experimental Allergic Conjunctivitis Córdova, Claudia Gutiérrez, Beatriz Martínez-García, Carmen Martín, Rubén Gallego-Muñoz, Patricia Hernández, Marita Nieto, María L. PLoS One Research Article Pollen is the most common aeroallergen to cause seasonal conjunctivitis. The result of allergen exposure is a strong Th2-mediated response along with conjunctival mast cell degranulation and eosinophilic infiltration. Oleanolic acid (OA) is natural a triterpene that displays strong anti-inflammatory and immunomodulatory properties being an active anti-allergic molecule on hypersensitivity reaction models. However, its effect on inflammatory ocular disorders including conjunctivits, has not yet been addressed. Hence, using a Ragweed pollen (RWP)-specific allergic conjunctivitis (EAC) mouse model we study here whether OA could modify responses associated to allergic processes. We found that OA treatment restricted mast cell degranulation and infiltration of eosinophils in conjunctival tissue and decreased allergen-specific Igs levels in EAC mice. Th2-type cytokines, secreted phospholipase A(2) type-IIA (sPLA(2)-IIA), and chemokines levels were also significantly diminished in the conjunctiva and serum of OA-treated EAC mice. Moreover, OA treatment also suppressed RWP-specific T-cell proliferation. In vitro studies, on relevant cells of the allergic process, revealed that OA reduced the proliferative and migratory response, as well as the synthesis of proinflammatory mediators on EoL-1 eosinophils and RBL-2H3 mast cells exposed to allergic and/or crucial inflammatory stimuli such as RWP, sPLA(2)-IIA or eotaxin. Taken together, these findings demonstrate the beneficial activity of OA in ocular allergic processes and may provide a new intervention strategy and potential therapy for allergic diseases. Public Library of Science 2014-04-03 /pmc/articles/PMC3974667/ /pubmed/24699261 http://dx.doi.org/10.1371/journal.pone.0091282 Text en © 2014 Córdova et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Córdova, Claudia
Gutiérrez, Beatriz
Martínez-García, Carmen
Martín, Rubén
Gallego-Muñoz, Patricia
Hernández, Marita
Nieto, María L.
Oleanolic Acid Controls Allergic and Inflammatory Responses in Experimental Allergic Conjunctivitis
title Oleanolic Acid Controls Allergic and Inflammatory Responses in Experimental Allergic Conjunctivitis
title_full Oleanolic Acid Controls Allergic and Inflammatory Responses in Experimental Allergic Conjunctivitis
title_fullStr Oleanolic Acid Controls Allergic and Inflammatory Responses in Experimental Allergic Conjunctivitis
title_full_unstemmed Oleanolic Acid Controls Allergic and Inflammatory Responses in Experimental Allergic Conjunctivitis
title_short Oleanolic Acid Controls Allergic and Inflammatory Responses in Experimental Allergic Conjunctivitis
title_sort oleanolic acid controls allergic and inflammatory responses in experimental allergic conjunctivitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974667/
https://www.ncbi.nlm.nih.gov/pubmed/24699261
http://dx.doi.org/10.1371/journal.pone.0091282
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