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Difructose dianhydride improves intestinal calcium absorption, wound healing, and barrier function
The gastrointestinal tract (GIT) is critical for nutrient absorption and is an important barrier against harmful pathogens and antigens. Difructose anhydrides (DFA)-IVs are nondigestible disaccharides that enhance calcium and iron absorption by affecting the intestinal epithelial tissue. However, th...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959885/ https://www.ncbi.nlm.nih.gov/pubmed/29777169 http://dx.doi.org/10.1038/s41598-018-26295-7 |
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author | Lee, Sang In Kim, In Ho |
author_facet | Lee, Sang In Kim, In Ho |
author_sort | Lee, Sang In |
collection | PubMed |
description | The gastrointestinal tract (GIT) is critical for nutrient absorption and is an important barrier against harmful pathogens and antigens. Difructose anhydrides (DFA)-IVs are nondigestible disaccharides that enhance calcium and iron absorption by affecting the intestinal epithelial tissue. However, their effects on intestinal functions are not fully understood. In this study, we performed a feeding trial and found that dietary DFA-IVs improved growth performance, relative breast muscle and liver weight, and digestibility and blood calcium and iron concentrations in broilers. Additionally, dietary DFA-IVs increased expression of genes related to growth in the liver, muscle development, and absorption of calcium and iron in the intestine. In vitro experiments revealed that DFA-IV treatment improved intestinal wound-healing (migration, proliferation, and differentiation) after lipopolysaccharide (LPS) challenge in small intestinal epithelial cells. Furthermore, DFA-IV treatment enhanced the intestinal barrier function, which increased the transepithelial electrical resistance (TEER) and decreased the permeability of fluorescein isothiocyanate-dextran (FD-4) after LPS challenge in small intestinal epithelial cells. Collectively, these data indicate that DFA-IV could be used as a feed additive to enhance calcium and iron absorption by affecting the intestinal wound healing and permeability. This study may help improve our understanding of the molecular effects of DFA-IV on the intestine. |
format | Online Article Text |
id | pubmed-5959885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59598852018-05-24 Difructose dianhydride improves intestinal calcium absorption, wound healing, and barrier function Lee, Sang In Kim, In Ho Sci Rep Article The gastrointestinal tract (GIT) is critical for nutrient absorption and is an important barrier against harmful pathogens and antigens. Difructose anhydrides (DFA)-IVs are nondigestible disaccharides that enhance calcium and iron absorption by affecting the intestinal epithelial tissue. However, their effects on intestinal functions are not fully understood. In this study, we performed a feeding trial and found that dietary DFA-IVs improved growth performance, relative breast muscle and liver weight, and digestibility and blood calcium and iron concentrations in broilers. Additionally, dietary DFA-IVs increased expression of genes related to growth in the liver, muscle development, and absorption of calcium and iron in the intestine. In vitro experiments revealed that DFA-IV treatment improved intestinal wound-healing (migration, proliferation, and differentiation) after lipopolysaccharide (LPS) challenge in small intestinal epithelial cells. Furthermore, DFA-IV treatment enhanced the intestinal barrier function, which increased the transepithelial electrical resistance (TEER) and decreased the permeability of fluorescein isothiocyanate-dextran (FD-4) after LPS challenge in small intestinal epithelial cells. Collectively, these data indicate that DFA-IV could be used as a feed additive to enhance calcium and iron absorption by affecting the intestinal wound healing and permeability. This study may help improve our understanding of the molecular effects of DFA-IV on the intestine. Nature Publishing Group UK 2018-05-18 /pmc/articles/PMC5959885/ /pubmed/29777169 http://dx.doi.org/10.1038/s41598-018-26295-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lee, Sang In Kim, In Ho Difructose dianhydride improves intestinal calcium absorption, wound healing, and barrier function |
title | Difructose dianhydride improves intestinal calcium absorption, wound healing, and barrier function |
title_full | Difructose dianhydride improves intestinal calcium absorption, wound healing, and barrier function |
title_fullStr | Difructose dianhydride improves intestinal calcium absorption, wound healing, and barrier function |
title_full_unstemmed | Difructose dianhydride improves intestinal calcium absorption, wound healing, and barrier function |
title_short | Difructose dianhydride improves intestinal calcium absorption, wound healing, and barrier function |
title_sort | difructose dianhydride improves intestinal calcium absorption, wound healing, and barrier function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959885/ https://www.ncbi.nlm.nih.gov/pubmed/29777169 http://dx.doi.org/10.1038/s41598-018-26295-7 |
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