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Effect of dietary additives on intestinal permeability in both Drosophila and a human cell co-culture
Increased intestinal barrier permeability has been correlated with aging and disease, including type 2 diabetes, Crohn's disease, celiac disease, multiple sclerosis and irritable bowel syndrome. The prevalence of these ailments has risen together with an increase in industrial food processing a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307910/ https://www.ncbi.nlm.nih.gov/pubmed/30504122 http://dx.doi.org/10.1242/dmm.034520 |
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author | Pereira, Matthew T. Malik, Mridu Nostro, Jillian A. Mahler, Gretchen J. Musselman, Laura Palanker |
author_facet | Pereira, Matthew T. Malik, Mridu Nostro, Jillian A. Mahler, Gretchen J. Musselman, Laura Palanker |
author_sort | Pereira, Matthew T. |
collection | PubMed |
description | Increased intestinal barrier permeability has been correlated with aging and disease, including type 2 diabetes, Crohn's disease, celiac disease, multiple sclerosis and irritable bowel syndrome. The prevalence of these ailments has risen together with an increase in industrial food processing and food additive consumption. Additives, including sugar, metal oxide nanoparticles, surfactants and sodium chloride, have all been suggested to increase intestinal permeability. We used two complementary model systems to examine the effects of food additives on gut barrier function: a Drosophila in vivo model and an in vitro human cell co-culture model. Of the additives tested, intestinal permeability was increased most dramatically by high sugar. High sugar also increased feeding but reduced gut and overall animal size. We also examined how food additives affected the activity of a gut mucosal defense factor, intestinal alkaline phosphatase (IAP), which fluctuates with bacterial load and affects intestinal permeability. We found that high sugar reduced IAP activity in both models. Artificial manipulation of the microbiome influenced gut permeability in both models, revealing a complex relationship between the two. This study extends previous work in flies and humans showing that diet can play a role in the health of the gut barrier. Moreover, simple models can be used to study mechanisms underlying the effects of diet on gut permeability and function. This article has an associated First Person interview with the first author of the paper. |
format | Online Article Text |
id | pubmed-6307910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63079102018-12-28 Effect of dietary additives on intestinal permeability in both Drosophila and a human cell co-culture Pereira, Matthew T. Malik, Mridu Nostro, Jillian A. Mahler, Gretchen J. Musselman, Laura Palanker Dis Model Mech Research Article Increased intestinal barrier permeability has been correlated with aging and disease, including type 2 diabetes, Crohn's disease, celiac disease, multiple sclerosis and irritable bowel syndrome. The prevalence of these ailments has risen together with an increase in industrial food processing and food additive consumption. Additives, including sugar, metal oxide nanoparticles, surfactants and sodium chloride, have all been suggested to increase intestinal permeability. We used two complementary model systems to examine the effects of food additives on gut barrier function: a Drosophila in vivo model and an in vitro human cell co-culture model. Of the additives tested, intestinal permeability was increased most dramatically by high sugar. High sugar also increased feeding but reduced gut and overall animal size. We also examined how food additives affected the activity of a gut mucosal defense factor, intestinal alkaline phosphatase (IAP), which fluctuates with bacterial load and affects intestinal permeability. We found that high sugar reduced IAP activity in both models. Artificial manipulation of the microbiome influenced gut permeability in both models, revealing a complex relationship between the two. This study extends previous work in flies and humans showing that diet can play a role in the health of the gut barrier. Moreover, simple models can be used to study mechanisms underlying the effects of diet on gut permeability and function. This article has an associated First Person interview with the first author of the paper. The Company of Biologists Ltd 2018-12-01 2018-11-28 /pmc/articles/PMC6307910/ /pubmed/30504122 http://dx.doi.org/10.1242/dmm.034520 Text en © 2018. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Pereira, Matthew T. Malik, Mridu Nostro, Jillian A. Mahler, Gretchen J. Musselman, Laura Palanker Effect of dietary additives on intestinal permeability in both Drosophila and a human cell co-culture |
title | Effect of dietary additives on intestinal permeability in both Drosophila and a human cell co-culture |
title_full | Effect of dietary additives on intestinal permeability in both Drosophila and a human cell co-culture |
title_fullStr | Effect of dietary additives on intestinal permeability in both Drosophila and a human cell co-culture |
title_full_unstemmed | Effect of dietary additives on intestinal permeability in both Drosophila and a human cell co-culture |
title_short | Effect of dietary additives on intestinal permeability in both Drosophila and a human cell co-culture |
title_sort | effect of dietary additives on intestinal permeability in both drosophila and a human cell co-culture |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307910/ https://www.ncbi.nlm.nih.gov/pubmed/30504122 http://dx.doi.org/10.1242/dmm.034520 |
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