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The effect of alpha linolenic acid on tracheal responsiveness, lung inflammation, and immune markers in sensitized rats
OBJECTIVE(S): The effects of alpha linolenic acid (ALA) on tracheal responsiveness (TR), total protein (TP), phospholipase A2 (PLA2), immunoglobulin E (IgE), interleukin 4 (IL-4), interferon gamma (INF-γ) level and INF-γ/IL4 ratio in bronchoalveolar lavage fluid (BALF) of sensitized rats were examin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528709/ https://www.ncbi.nlm.nih.gov/pubmed/31156785 http://dx.doi.org/10.22038/ijbms.2019.27381.6684 |
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author | Kaveh, Mahsa Eftekhar, Naeima Boskabady, Mohammad Hossein |
author_facet | Kaveh, Mahsa Eftekhar, Naeima Boskabady, Mohammad Hossein |
author_sort | Kaveh, Mahsa |
collection | PubMed |
description | OBJECTIVE(S): The effects of alpha linolenic acid (ALA) on tracheal responsiveness (TR), total protein (TP), phospholipase A2 (PLA2), immunoglobulin E (IgE), interleukin 4 (IL-4), interferon gamma (INF-γ) level and INF-γ/IL4 ratio in bronchoalveolar lavage fluid (BALF) of sensitized rats were examined. MATERIALS AND METHODS: TR to methacholine and ovalbumin (OA), BALF levels of TP, PLA2 and IgE as well as IL-4, INF-γ and INF-γ/IL4 ratio were measured in control group (non-sensitized, group C), sensitized rats to OA (group S), S groups treated with two concentrations of ALA and dexamethasone group. RESULTS: TR to methacholine and OA, BALF levels of TP, PLA2, IgE and IL-4 were significantly increased but BALF level of INF-γ and INF-γ/IL4 ratio decreased in group S compared to group C (P<0.001 for all cases). Treated S groups with dexamethasone and both concentrations of ALA lead to significant decrease in TR to methacholine and OA, BALF levels of TP, PLA2, IgE and IL-4 compared to group S (P<0.001 for all case). The effects of all concentrations of ALA on INF-γ, IL-4 and INF-γ/IL4 ratio and also the effect of its highest concentration on TP and IgE level were significantly higher than dexamethasone treatment (P<0.001 for all cases). CONCLUSION: Results showed an immune modulatory effect of the ALA that increased INF-γ, INF-γ/IL4 ratio (as an index of Th1/Th2) and decreased IL-4 in sensitized rats. ALA also showed preventive effect on inflammatory markers and tracheal responsiveness in sensitized animals comparable to the effect of dexamethasone. |
format | Online Article Text |
id | pubmed-6528709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-65287092019-05-31 The effect of alpha linolenic acid on tracheal responsiveness, lung inflammation, and immune markers in sensitized rats Kaveh, Mahsa Eftekhar, Naeima Boskabady, Mohammad Hossein Iran J Basic Med Sci Original Article OBJECTIVE(S): The effects of alpha linolenic acid (ALA) on tracheal responsiveness (TR), total protein (TP), phospholipase A2 (PLA2), immunoglobulin E (IgE), interleukin 4 (IL-4), interferon gamma (INF-γ) level and INF-γ/IL4 ratio in bronchoalveolar lavage fluid (BALF) of sensitized rats were examined. MATERIALS AND METHODS: TR to methacholine and ovalbumin (OA), BALF levels of TP, PLA2 and IgE as well as IL-4, INF-γ and INF-γ/IL4 ratio were measured in control group (non-sensitized, group C), sensitized rats to OA (group S), S groups treated with two concentrations of ALA and dexamethasone group. RESULTS: TR to methacholine and OA, BALF levels of TP, PLA2, IgE and IL-4 were significantly increased but BALF level of INF-γ and INF-γ/IL4 ratio decreased in group S compared to group C (P<0.001 for all cases). Treated S groups with dexamethasone and both concentrations of ALA lead to significant decrease in TR to methacholine and OA, BALF levels of TP, PLA2, IgE and IL-4 compared to group S (P<0.001 for all case). The effects of all concentrations of ALA on INF-γ, IL-4 and INF-γ/IL4 ratio and also the effect of its highest concentration on TP and IgE level were significantly higher than dexamethasone treatment (P<0.001 for all cases). CONCLUSION: Results showed an immune modulatory effect of the ALA that increased INF-γ, INF-γ/IL4 ratio (as an index of Th1/Th2) and decreased IL-4 in sensitized rats. ALA also showed preventive effect on inflammatory markers and tracheal responsiveness in sensitized animals comparable to the effect of dexamethasone. Mashhad University of Medical Sciences 2019-03 /pmc/articles/PMC6528709/ /pubmed/31156785 http://dx.doi.org/10.22038/ijbms.2019.27381.6684 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kaveh, Mahsa Eftekhar, Naeima Boskabady, Mohammad Hossein The effect of alpha linolenic acid on tracheal responsiveness, lung inflammation, and immune markers in sensitized rats |
title | The effect of alpha linolenic acid on tracheal responsiveness, lung inflammation, and immune markers in sensitized rats |
title_full | The effect of alpha linolenic acid on tracheal responsiveness, lung inflammation, and immune markers in sensitized rats |
title_fullStr | The effect of alpha linolenic acid on tracheal responsiveness, lung inflammation, and immune markers in sensitized rats |
title_full_unstemmed | The effect of alpha linolenic acid on tracheal responsiveness, lung inflammation, and immune markers in sensitized rats |
title_short | The effect of alpha linolenic acid on tracheal responsiveness, lung inflammation, and immune markers in sensitized rats |
title_sort | effect of alpha linolenic acid on tracheal responsiveness, lung inflammation, and immune markers in sensitized rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528709/ https://www.ncbi.nlm.nih.gov/pubmed/31156785 http://dx.doi.org/10.22038/ijbms.2019.27381.6684 |
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