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Enzymatically synthesized glycogen inhibited degranulation and inflammatory responses through stimulation of intestine
The patients of type I allergic diseases were increased in the developed countries. Recently, many studies have focused on food factors with anti-allergic activities. Enzymatically synthesized glycogen, a polysaccharide with a multi-branched α-1,4 and α-1,6 linkages, is a commercially available prod...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417801/ https://www.ncbi.nlm.nih.gov/pubmed/32801471 http://dx.doi.org/10.3164/jcbn.20-33 |
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author | Yoshioka, Yasukiyo Inoue, Masako Yoshioka, Hiroko Kitakaze, Tomoya Furuyashiki, Takashi Abe, Naoki Ashida, Hitoshi |
author_facet | Yoshioka, Yasukiyo Inoue, Masako Yoshioka, Hiroko Kitakaze, Tomoya Furuyashiki, Takashi Abe, Naoki Ashida, Hitoshi |
author_sort | Yoshioka, Yasukiyo |
collection | PubMed |
description | The patients of type I allergic diseases were increased in the developed countries. Recently, many studies have focused on food factors with anti-allergic activities. Enzymatically synthesized glycogen, a polysaccharide with a multi-branched α-1,4 and α-1,6 linkages, is a commercially available product from natural plant starch, and has immunostimulation activity. However, effect of enzymatically synthesized glycogen on the anti-allergic activity was unclear yet. In this study, we investigated that enzymatically synthesized glycogen inhibited allergic and inflammatory responses using a co-culture system consisting of Caco-2 and RBL-2H3 cells. Enzymatically synthesized glycogen inhibited antigen-induced β-hexosaminidase release and production of TNF-α and IL-6 in RBL-2H3 cells in the co-culture system. Furthermore, enzymatically synthesized glycogen inhibited antigen-induced phosphorylation of tyrosine kinases, phospholipase C γ1/2, mitogen-activated protein kinases and Akt. Anti-allergic and anti-inflammatory activities of enzymatically synthesized glycogen were indirect action through stimulating Caco-2 cells, but not by the direct interaction with RBL-2H3 cells, because enzymatically synthesized glycogen did not permeate Caco-2 cells. These findings suggest that enzymatically synthesized glycogen is an effective food ingredient for prevention of type I allergy through stimulating the intestinal cells. |
format | Online Article Text |
id | pubmed-7417801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-74178012020-08-13 Enzymatically synthesized glycogen inhibited degranulation and inflammatory responses through stimulation of intestine Yoshioka, Yasukiyo Inoue, Masako Yoshioka, Hiroko Kitakaze, Tomoya Furuyashiki, Takashi Abe, Naoki Ashida, Hitoshi J Clin Biochem Nutr Original Article The patients of type I allergic diseases were increased in the developed countries. Recently, many studies have focused on food factors with anti-allergic activities. Enzymatically synthesized glycogen, a polysaccharide with a multi-branched α-1,4 and α-1,6 linkages, is a commercially available product from natural plant starch, and has immunostimulation activity. However, effect of enzymatically synthesized glycogen on the anti-allergic activity was unclear yet. In this study, we investigated that enzymatically synthesized glycogen inhibited allergic and inflammatory responses using a co-culture system consisting of Caco-2 and RBL-2H3 cells. Enzymatically synthesized glycogen inhibited antigen-induced β-hexosaminidase release and production of TNF-α and IL-6 in RBL-2H3 cells in the co-culture system. Furthermore, enzymatically synthesized glycogen inhibited antigen-induced phosphorylation of tyrosine kinases, phospholipase C γ1/2, mitogen-activated protein kinases and Akt. Anti-allergic and anti-inflammatory activities of enzymatically synthesized glycogen were indirect action through stimulating Caco-2 cells, but not by the direct interaction with RBL-2H3 cells, because enzymatically synthesized glycogen did not permeate Caco-2 cells. These findings suggest that enzymatically synthesized glycogen is an effective food ingredient for prevention of type I allergy through stimulating the intestinal cells. the Society for Free Radical Research Japan 2020-07 2020-06-05 /pmc/articles/PMC7417801/ /pubmed/32801471 http://dx.doi.org/10.3164/jcbn.20-33 Text en Copyright © 2020 JCBN http://creativecommons.org/licenses/by/3.0/ 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 work is properly cited. |
spellingShingle | Original Article Yoshioka, Yasukiyo Inoue, Masako Yoshioka, Hiroko Kitakaze, Tomoya Furuyashiki, Takashi Abe, Naoki Ashida, Hitoshi Enzymatically synthesized glycogen inhibited degranulation and inflammatory responses through stimulation of intestine |
title | Enzymatically synthesized glycogen inhibited degranulation and inflammatory responses through stimulation of intestine |
title_full | Enzymatically synthesized glycogen inhibited degranulation and inflammatory responses through stimulation of intestine |
title_fullStr | Enzymatically synthesized glycogen inhibited degranulation and inflammatory responses through stimulation of intestine |
title_full_unstemmed | Enzymatically synthesized glycogen inhibited degranulation and inflammatory responses through stimulation of intestine |
title_short | Enzymatically synthesized glycogen inhibited degranulation and inflammatory responses through stimulation of intestine |
title_sort | enzymatically synthesized glycogen inhibited degranulation and inflammatory responses through stimulation of intestine |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417801/ https://www.ncbi.nlm.nih.gov/pubmed/32801471 http://dx.doi.org/10.3164/jcbn.20-33 |
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