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Preventive Effect of Novel Bacterial Polysaccharide and Animal Splenic Protein as Natural Adjuvants on Animal Model of Asthma

OBJECTIVE(S): Two new adjuvants from natural animal lipids (G2) and bacterial polysaccharide extracts (PC) were previously prepared by our group and showed a reduction in tracheal responsiveness. The aim of this study was to evaluate the preventive effect of recently introduced natural products (G2...

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Autores principales: Mirsadraee, Majid, Mohaghegh Hazrati, Saleh, Khakzad, Mohammad Reza, Ghafarzadegan, Kamran, Boskabady, Mohhamad Hosein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586916/
https://www.ncbi.nlm.nih.gov/pubmed/23493252
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author Mirsadraee, Majid
Mohaghegh Hazrati, Saleh
Khakzad, Mohammad Reza
Ghafarzadegan, Kamran
Boskabady, Mohhamad Hosein
author_facet Mirsadraee, Majid
Mohaghegh Hazrati, Saleh
Khakzad, Mohammad Reza
Ghafarzadegan, Kamran
Boskabady, Mohhamad Hosein
author_sort Mirsadraee, Majid
collection PubMed
description OBJECTIVE(S): Two new adjuvants from natural animal lipids (G2) and bacterial polysaccharide extracts (PC) were previously prepared by our group and showed a reduction in tracheal responsiveness. The aim of this study was to evaluate the preventive effect of recently introduced natural products (G2 and PC) on the development of asthma. MATERIALS AND METHODS: Asthma was induced using a standard method in four groups of BALB/c mice. A non-sensitized control group was also included in order to be compared with treated groups. Three groups were premedicated with novel agents named G2, PC, and a combination of these two for 20 days before starting the induction of asthma. Bronchoalveolar lavage fluid (BALF) was collected and analyzed for inflammatory cells. Interferon-γ, and IL-4 and the histopathological of both lungs were also evaluated. RESULTS: In all pretreated groups, the inflammatory cells infiltration especially eosinophils and smooth muscle hyperplasia decreased significantly. BALF cytology also showed significant decrease in eosinophil count in all pretreated groups. There was a significant increase in the BALF and serum INF-γ in all pretreated groups but the combination of G2/PC was more effective. BALF IL-4 decreased significantly in the group pretreated with a combination of G2 and G2/PC (4.11±0.86 and 4.02±0.52 pg/ml in G2 and G2/PC, respectively). Serum IL-4 in the PC group was significantly higher than the sensitized control. CONCLUSION: G2 and PC may effectively prevent asthma development by activation of the type 1 T helper system.
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spelling pubmed-35869162013-03-14 Preventive Effect of Novel Bacterial Polysaccharide and Animal Splenic Protein as Natural Adjuvants on Animal Model of Asthma Mirsadraee, Majid Mohaghegh Hazrati, Saleh Khakzad, Mohammad Reza Ghafarzadegan, Kamran Boskabady, Mohhamad Hosein Iran J Basic Med Sci Original Article OBJECTIVE(S): Two new adjuvants from natural animal lipids (G2) and bacterial polysaccharide extracts (PC) were previously prepared by our group and showed a reduction in tracheal responsiveness. The aim of this study was to evaluate the preventive effect of recently introduced natural products (G2 and PC) on the development of asthma. MATERIALS AND METHODS: Asthma was induced using a standard method in four groups of BALB/c mice. A non-sensitized control group was also included in order to be compared with treated groups. Three groups were premedicated with novel agents named G2, PC, and a combination of these two for 20 days before starting the induction of asthma. Bronchoalveolar lavage fluid (BALF) was collected and analyzed for inflammatory cells. Interferon-γ, and IL-4 and the histopathological of both lungs were also evaluated. RESULTS: In all pretreated groups, the inflammatory cells infiltration especially eosinophils and smooth muscle hyperplasia decreased significantly. BALF cytology also showed significant decrease in eosinophil count in all pretreated groups. There was a significant increase in the BALF and serum INF-γ in all pretreated groups but the combination of G2/PC was more effective. BALF IL-4 decreased significantly in the group pretreated with a combination of G2 and G2/PC (4.11±0.86 and 4.02±0.52 pg/ml in G2 and G2/PC, respectively). Serum IL-4 in the PC group was significantly higher than the sensitized control. CONCLUSION: G2 and PC may effectively prevent asthma development by activation of the type 1 T helper system. Mashhad University of Medical Sciences 2012 /pmc/articles/PMC3586916/ /pubmed/23493252 Text en © 2012: Iranian Journal of Basic Medical Sciences 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
Mirsadraee, Majid
Mohaghegh Hazrati, Saleh
Khakzad, Mohammad Reza
Ghafarzadegan, Kamran
Boskabady, Mohhamad Hosein
Preventive Effect of Novel Bacterial Polysaccharide and Animal Splenic Protein as Natural Adjuvants on Animal Model of Asthma
title Preventive Effect of Novel Bacterial Polysaccharide and Animal Splenic Protein as Natural Adjuvants on Animal Model of Asthma
title_full Preventive Effect of Novel Bacterial Polysaccharide and Animal Splenic Protein as Natural Adjuvants on Animal Model of Asthma
title_fullStr Preventive Effect of Novel Bacterial Polysaccharide and Animal Splenic Protein as Natural Adjuvants on Animal Model of Asthma
title_full_unstemmed Preventive Effect of Novel Bacterial Polysaccharide and Animal Splenic Protein as Natural Adjuvants on Animal Model of Asthma
title_short Preventive Effect of Novel Bacterial Polysaccharide and Animal Splenic Protein as Natural Adjuvants on Animal Model of Asthma
title_sort preventive effect of novel bacterial polysaccharide and animal splenic protein as natural adjuvants on animal model of asthma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586916/
https://www.ncbi.nlm.nih.gov/pubmed/23493252
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