Cargando…
Haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation
BACKGROUND: The World Health Organization classified processed and red meat consumption as “carcinogenic” and “probably carcinogenic”, respectively, to humans. Haem iron from meat plays a role in the promotion of colorectal cancer in rodent models, in association with enhanced luminal lipoperoxidati...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503375/ https://www.ncbi.nlm.nih.gov/pubmed/31060614 http://dx.doi.org/10.1186/s40168-019-0685-7 |
_version_ | 1783416397689257984 |
---|---|
author | Martin, Océane C. B. Olier, Maïwenn Ellero-Simatos, Sandrine Naud, Nathalie Dupuy, Jacques Huc, Laurence Taché, Sylviane Graillot, Vanessa Levêque, Mathilde Bézirard, Valérie Héliès-Toussaint, Cécile Estrada, Florence Blas Y. Tondereau, Valérie Lippi, Yannick Naylies, Claire Peyriga, Lindsey Canlet, Cécile Davila, Anne Marie Blachier, François Ferrier, Laurent Boutet-Robinet, Elisa Guéraud, Françoise Théodorou, Vassilia Pierre, Fabrice H. F. |
author_facet | Martin, Océane C. B. Olier, Maïwenn Ellero-Simatos, Sandrine Naud, Nathalie Dupuy, Jacques Huc, Laurence Taché, Sylviane Graillot, Vanessa Levêque, Mathilde Bézirard, Valérie Héliès-Toussaint, Cécile Estrada, Florence Blas Y. Tondereau, Valérie Lippi, Yannick Naylies, Claire Peyriga, Lindsey Canlet, Cécile Davila, Anne Marie Blachier, François Ferrier, Laurent Boutet-Robinet, Elisa Guéraud, Françoise Théodorou, Vassilia Pierre, Fabrice H. F. |
author_sort | Martin, Océane C. B. |
collection | PubMed |
description | BACKGROUND: The World Health Organization classified processed and red meat consumption as “carcinogenic” and “probably carcinogenic”, respectively, to humans. Haem iron from meat plays a role in the promotion of colorectal cancer in rodent models, in association with enhanced luminal lipoperoxidation and subsequent formation of aldehydes. Here, we investigated the short-term effects of this haem-induced lipoperoxidation on mucosal and luminal gut homeostasis including microbiome in F344 male rats fed with a haem-enriched diet (1.5 μmol/g) 14–21 days. RESULTS: Changes in permeability, inflammation, and genotoxicity observed in the mucosal colonic barrier correlated with luminal haem and lipoperoxidation markers. Trapping of luminal haem-induced aldehydes normalised cellular genotoxicity, permeability, and ROS formation on a colon epithelial cell line. Addition of calcium carbonate (2%) to the haem-enriched diet allowed the luminal haem to be trapped in vivo and counteracted these haem-induced physiological traits. Similar covariations of faecal metabolites and bacterial taxa according to haem-induced lipoperoxidation were identified. CONCLUSIONS: This integrated approach provides an overview of haem-induced modulations of the main actors in the colonic barrier. All alterations were closely linked to haem-induced lipoperoxidation, which is associated with red meat-induced colorectal cancer risk. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0685-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6503375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65033752019-05-10 Haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation Martin, Océane C. B. Olier, Maïwenn Ellero-Simatos, Sandrine Naud, Nathalie Dupuy, Jacques Huc, Laurence Taché, Sylviane Graillot, Vanessa Levêque, Mathilde Bézirard, Valérie Héliès-Toussaint, Cécile Estrada, Florence Blas Y. Tondereau, Valérie Lippi, Yannick Naylies, Claire Peyriga, Lindsey Canlet, Cécile Davila, Anne Marie Blachier, François Ferrier, Laurent Boutet-Robinet, Elisa Guéraud, Françoise Théodorou, Vassilia Pierre, Fabrice H. F. Microbiome Research BACKGROUND: The World Health Organization classified processed and red meat consumption as “carcinogenic” and “probably carcinogenic”, respectively, to humans. Haem iron from meat plays a role in the promotion of colorectal cancer in rodent models, in association with enhanced luminal lipoperoxidation and subsequent formation of aldehydes. Here, we investigated the short-term effects of this haem-induced lipoperoxidation on mucosal and luminal gut homeostasis including microbiome in F344 male rats fed with a haem-enriched diet (1.5 μmol/g) 14–21 days. RESULTS: Changes in permeability, inflammation, and genotoxicity observed in the mucosal colonic barrier correlated with luminal haem and lipoperoxidation markers. Trapping of luminal haem-induced aldehydes normalised cellular genotoxicity, permeability, and ROS formation on a colon epithelial cell line. Addition of calcium carbonate (2%) to the haem-enriched diet allowed the luminal haem to be trapped in vivo and counteracted these haem-induced physiological traits. Similar covariations of faecal metabolites and bacterial taxa according to haem-induced lipoperoxidation were identified. CONCLUSIONS: This integrated approach provides an overview of haem-induced modulations of the main actors in the colonic barrier. All alterations were closely linked to haem-induced lipoperoxidation, which is associated with red meat-induced colorectal cancer risk. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0685-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-06 /pmc/articles/PMC6503375/ /pubmed/31060614 http://dx.doi.org/10.1186/s40168-019-0685-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Martin, Océane C. B. Olier, Maïwenn Ellero-Simatos, Sandrine Naud, Nathalie Dupuy, Jacques Huc, Laurence Taché, Sylviane Graillot, Vanessa Levêque, Mathilde Bézirard, Valérie Héliès-Toussaint, Cécile Estrada, Florence Blas Y. Tondereau, Valérie Lippi, Yannick Naylies, Claire Peyriga, Lindsey Canlet, Cécile Davila, Anne Marie Blachier, François Ferrier, Laurent Boutet-Robinet, Elisa Guéraud, Françoise Théodorou, Vassilia Pierre, Fabrice H. F. Haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation |
title | Haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation |
title_full | Haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation |
title_fullStr | Haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation |
title_full_unstemmed | Haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation |
title_short | Haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation |
title_sort | haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503375/ https://www.ncbi.nlm.nih.gov/pubmed/31060614 http://dx.doi.org/10.1186/s40168-019-0685-7 |
work_keys_str_mv | AT martinoceanecb haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT oliermaiwenn haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT ellerosimatossandrine haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT naudnathalie haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT dupuyjacques haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT huclaurence haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT tachesylviane haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT graillotvanessa haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT levequemathilde haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT bezirardvalerie haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT heliestoussaintcecile haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT estradaflorenceblasy haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT tondereauvalerie haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT lippiyannick haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT nayliesclaire haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT peyrigalindsey haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT canletcecile haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT davilaannemarie haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT blachierfrancois haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT ferrierlaurent haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT boutetrobinetelisa haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT gueraudfrancoise haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT theodorouvassilia haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation AT pierrefabricehf haemironreshapescolonicluminalenvironmentimpactonmucosalhomeostasisandmicrobiomethroughaldehydeformation |