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Anti-allergic effect of luteolin in mice with allergic asthma and rhinitis

AIM OF THE STUDY: We aimed to evaluate the anti-allergic effect of luteolin treatment in mice with allergic asthma and rhinitis. MATERIAL AND METHODS: Thirty-two BALB/c mice (n = 8 for each group) were used. Mice in group A (nonallergic group) were exposed to saline, while those in Group B (allergic...

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Autores principales: Jang, Tae Young, Jung, Ah-Yeoun, Kyung, Tae-Suk, Kim, Dae-Young, Hwang, Jun-Ha, Kim, Young Hyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470611/
https://www.ncbi.nlm.nih.gov/pubmed/28680328
http://dx.doi.org/10.5114/ceji.2017.67315
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author Jang, Tae Young
Jung, Ah-Yeoun
Kyung, Tae-Suk
Kim, Dae-Young
Hwang, Jun-Ha
Kim, Young Hyo
author_facet Jang, Tae Young
Jung, Ah-Yeoun
Kyung, Tae-Suk
Kim, Dae-Young
Hwang, Jun-Ha
Kim, Young Hyo
author_sort Jang, Tae Young
collection PubMed
description AIM OF THE STUDY: We aimed to evaluate the anti-allergic effect of luteolin treatment in mice with allergic asthma and rhinitis. MATERIAL AND METHODS: Thirty-two BALB/c mice (n = 8 for each group) were used. Mice in group A (nonallergic group) were exposed to saline, while those in Group B (allergic group) were exposed to ovalbumin (OVA) intraperitoneal (i.p.) injection and intranasal (i.n.) challenge. Null treatment group (Group C) received sterile saline (150 μl) i.p. injection, 30 minutes before each i.n. challenge. Finally, the treatment group (Group D) received luteolin (0.1 mg/kg) by i.p. injection, 30 minutes before each i.n. challenge. We evaluated the number of inflammatory cells including eosinophils, neutrophils and lymphocytes in bronchoalveolar lavage (BAL) fluid, the titers of IL-4, IL-5 and IL-13 in lung homogenate, and we also evaluated histopathologic findings, including infiltration of inflammatory cells into the pulmonary parenchyma and nasal mucosa. RESULTS: After the OVA challenge, the number of eosinophils, neutrophils and lymphocytes in BAL fluid was significantly increased in group B, compared to group A (p < 0.001). Mice in group C had no significant difference (p > 0.05). On the other hand, group D showed a significant decrease in all inflammatory cells compared to group B (p < 0.05). Also, group D showed a significant decrease in IL-4, IL-5 and IL-13 in their lung homogenate compared to groups B and C (p < 0.05). Group D also showed a significant decrease in inflammatory cell infiltration after luteolin treatment (p < 0.05). CONCLUSION: Luteolin had an anti-allergic effect in a murine model of allergic asthma and rhinitis.
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spelling pubmed-54706112017-07-05 Anti-allergic effect of luteolin in mice with allergic asthma and rhinitis Jang, Tae Young Jung, Ah-Yeoun Kyung, Tae-Suk Kim, Dae-Young Hwang, Jun-Ha Kim, Young Hyo Cent Eur J Immunol Experimental Immunology AIM OF THE STUDY: We aimed to evaluate the anti-allergic effect of luteolin treatment in mice with allergic asthma and rhinitis. MATERIAL AND METHODS: Thirty-two BALB/c mice (n = 8 for each group) were used. Mice in group A (nonallergic group) were exposed to saline, while those in Group B (allergic group) were exposed to ovalbumin (OVA) intraperitoneal (i.p.) injection and intranasal (i.n.) challenge. Null treatment group (Group C) received sterile saline (150 μl) i.p. injection, 30 minutes before each i.n. challenge. Finally, the treatment group (Group D) received luteolin (0.1 mg/kg) by i.p. injection, 30 minutes before each i.n. challenge. We evaluated the number of inflammatory cells including eosinophils, neutrophils and lymphocytes in bronchoalveolar lavage (BAL) fluid, the titers of IL-4, IL-5 and IL-13 in lung homogenate, and we also evaluated histopathologic findings, including infiltration of inflammatory cells into the pulmonary parenchyma and nasal mucosa. RESULTS: After the OVA challenge, the number of eosinophils, neutrophils and lymphocytes in BAL fluid was significantly increased in group B, compared to group A (p < 0.001). Mice in group C had no significant difference (p > 0.05). On the other hand, group D showed a significant decrease in all inflammatory cells compared to group B (p < 0.05). Also, group D showed a significant decrease in IL-4, IL-5 and IL-13 in their lung homogenate compared to groups B and C (p < 0.05). Group D also showed a significant decrease in inflammatory cell infiltration after luteolin treatment (p < 0.05). CONCLUSION: Luteolin had an anti-allergic effect in a murine model of allergic asthma and rhinitis. Polish Society of Experimental and Clinical Immunology 2017-05-08 2017 /pmc/articles/PMC5470611/ /pubmed/28680328 http://dx.doi.org/10.5114/ceji.2017.67315 Text en Copyright: © 2017 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Experimental Immunology
Jang, Tae Young
Jung, Ah-Yeoun
Kyung, Tae-Suk
Kim, Dae-Young
Hwang, Jun-Ha
Kim, Young Hyo
Anti-allergic effect of luteolin in mice with allergic asthma and rhinitis
title Anti-allergic effect of luteolin in mice with allergic asthma and rhinitis
title_full Anti-allergic effect of luteolin in mice with allergic asthma and rhinitis
title_fullStr Anti-allergic effect of luteolin in mice with allergic asthma and rhinitis
title_full_unstemmed Anti-allergic effect of luteolin in mice with allergic asthma and rhinitis
title_short Anti-allergic effect of luteolin in mice with allergic asthma and rhinitis
title_sort anti-allergic effect of luteolin in mice with allergic asthma and rhinitis
topic Experimental Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470611/
https://www.ncbi.nlm.nih.gov/pubmed/28680328
http://dx.doi.org/10.5114/ceji.2017.67315
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