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Endogenous mucin conveyed to the mucosa with microbes can assure lumen fermentation and large intestinal security–swine versus fowl

Endogenous protein leaving the ileum largely consists of accrued mucins from the upper gastrointestinal tract (GIT) that had resisted digestion. The amounts released rely on their mucosal generation during enteral feeding which vary with age as well as diet. These digestion resistant proteins of end...

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Autores principales: Moran, Edwin T., Bedford, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457508/
https://www.ncbi.nlm.nih.gov/pubmed/37635931
http://dx.doi.org/10.1016/j.aninu.2023.06.010
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author Moran, Edwin T.
Bedford, Michael R.
author_facet Moran, Edwin T.
Bedford, Michael R.
author_sort Moran, Edwin T.
collection PubMed
description Endogenous protein leaving the ileum largely consists of accrued mucins from the upper gastrointestinal tract (GIT) that had resisted digestion. The amounts released rely on their mucosal generation during enteral feeding which vary with age as well as diet. These digestion resistant proteins of endogenous origin continue to be unavailable in the large intestine, whereas those of dietary origin provide amino acids that largely support the existing microbial population while denying limited amounts for absorption. Other mucins pre-exist within the large intestine as two layers at the lumen surface. A loose layer harboring a diverse microbial population is superimposed on the unstirred water layer (USWL) which simultaneously acts as an obstacle to microbes at the loose layer while performing as a molecular sieve for nutrients. The USWL is formed through interplay between enterocyte and goblet cells; however, the basis for presence of the loose layer is elusive. Large intestinal fermentation predominates within the colon of swine, whereas fowl employ their ceca. Motility within the colon of swine segregates fine materials into haustrae out-pocketings that parallel their placement within the ceca of fowl. Viscous mucins from small intestinal endogenous losses may envelop microbes within the large intestinal lumen to present successive adherents on the USWL that assemble its loose layer. The loose layer continually functions as a microbial reservoir in support of lumen fermentation. Microbial catabolism of mucin within the loose layer is known to be slow, but its proximity to the enterocyte is of advantage to enterocyte absorption with by-product amino acids fostering the USWL.
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spelling pubmed-104575082023-08-27 Endogenous mucin conveyed to the mucosa with microbes can assure lumen fermentation and large intestinal security–swine versus fowl Moran, Edwin T. Bedford, Michael R. Anim Nutr Review Article Endogenous protein leaving the ileum largely consists of accrued mucins from the upper gastrointestinal tract (GIT) that had resisted digestion. The amounts released rely on their mucosal generation during enteral feeding which vary with age as well as diet. These digestion resistant proteins of endogenous origin continue to be unavailable in the large intestine, whereas those of dietary origin provide amino acids that largely support the existing microbial population while denying limited amounts for absorption. Other mucins pre-exist within the large intestine as two layers at the lumen surface. A loose layer harboring a diverse microbial population is superimposed on the unstirred water layer (USWL) which simultaneously acts as an obstacle to microbes at the loose layer while performing as a molecular sieve for nutrients. The USWL is formed through interplay between enterocyte and goblet cells; however, the basis for presence of the loose layer is elusive. Large intestinal fermentation predominates within the colon of swine, whereas fowl employ their ceca. Motility within the colon of swine segregates fine materials into haustrae out-pocketings that parallel their placement within the ceca of fowl. Viscous mucins from small intestinal endogenous losses may envelop microbes within the large intestinal lumen to present successive adherents on the USWL that assemble its loose layer. The loose layer continually functions as a microbial reservoir in support of lumen fermentation. Microbial catabolism of mucin within the loose layer is known to be slow, but its proximity to the enterocyte is of advantage to enterocyte absorption with by-product amino acids fostering the USWL. KeAi Publishing 2023-07-12 /pmc/articles/PMC10457508/ /pubmed/37635931 http://dx.doi.org/10.1016/j.aninu.2023.06.010 Text en © 2023 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Moran, Edwin T.
Bedford, Michael R.
Endogenous mucin conveyed to the mucosa with microbes can assure lumen fermentation and large intestinal security–swine versus fowl
title Endogenous mucin conveyed to the mucosa with microbes can assure lumen fermentation and large intestinal security–swine versus fowl
title_full Endogenous mucin conveyed to the mucosa with microbes can assure lumen fermentation and large intestinal security–swine versus fowl
title_fullStr Endogenous mucin conveyed to the mucosa with microbes can assure lumen fermentation and large intestinal security–swine versus fowl
title_full_unstemmed Endogenous mucin conveyed to the mucosa with microbes can assure lumen fermentation and large intestinal security–swine versus fowl
title_short Endogenous mucin conveyed to the mucosa with microbes can assure lumen fermentation and large intestinal security–swine versus fowl
title_sort endogenous mucin conveyed to the mucosa with microbes can assure lumen fermentation and large intestinal security–swine versus fowl
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457508/
https://www.ncbi.nlm.nih.gov/pubmed/37635931
http://dx.doi.org/10.1016/j.aninu.2023.06.010
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