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Modulation of Intestinal Microbiome Prevents Intestinal Ischemic Injury

Background: Butyrate protects against ischemic injury to the small intestine by reducing inflammation and maintaining the structure of the intestinal barrier, but is expensive, short-lived, and cannot be administered easily due to its odor. Lactate, both economical and more palatable, can be convert...

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Autores principales: Bertacco, Alessandra, Dehner, Carina A., Caturegli, Giorgio, D'Amico, Francesco, Morotti, Raffaella, Rodriguez, Manuel I., Mulligan, David C., Kriegel, Martin A., Geibel, John P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742259/
https://www.ncbi.nlm.nih.gov/pubmed/29311987
http://dx.doi.org/10.3389/fphys.2017.01064
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author Bertacco, Alessandra
Dehner, Carina A.
Caturegli, Giorgio
D'Amico, Francesco
Morotti, Raffaella
Rodriguez, Manuel I.
Mulligan, David C.
Kriegel, Martin A.
Geibel, John P.
author_facet Bertacco, Alessandra
Dehner, Carina A.
Caturegli, Giorgio
D'Amico, Francesco
Morotti, Raffaella
Rodriguez, Manuel I.
Mulligan, David C.
Kriegel, Martin A.
Geibel, John P.
author_sort Bertacco, Alessandra
collection PubMed
description Background: Butyrate protects against ischemic injury to the small intestine by reducing inflammation and maintaining the structure of the intestinal barrier, but is expensive, short-lived, and cannot be administered easily due to its odor. Lactate, both economical and more palatable, can be converted into butyrate by the intestinal microbiome. This study aimed to assess in a rat model whether lactate perfusion can also protect against intestinal ischemia. Materials and Methods: Rat intestinal segments were loaded in an in vitro bowel perfusion device, and water absorption or secretion was assessed based on fluorescence of FITC-inulin, a fluorescent marker bound to a biologically inert sugar. Change in FITC concentration was used as a measure of ischemic injury, given the tendency of ischemic cells to retain water. Hematoxylin and eosin-stained sections at light level microscopy were examined to evaluate intestinal epithelium morphology. Comparisons between the data sets were paired Student t-tests or ANOVA with p < 0.05 performed on GraphPad. Results: Lactate administration resulted in a protective effect against intestinal ischemia of similar magnitude to that observed with butyrate. Both exhibited approximately 1.5 times the secretion exhibited by control sections (p = 0.03). Perfusion with lactate and methoxyacetate, a specific inhibitor of lactate-butyrate conversion, abolished this effect (p = 0.09). Antibiotic treatment also eliminated this effect, rendering lactate-perfused sections similar to control sections (p = 0.72). Perfusion with butyrate and methoxyacetate did not eliminate the observed increased secretion, which indicates that ischemic protection was mediated by microbial conversion of lactate to butyrate (p = 0.71). Conclusions: Lactate's protective effect against intestinal ischemia due to microbial conversion to butyrate suggests possible applications in the transplant setting for reducing ischemic injury and ameliorating intestinal preservation during transport.
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spelling pubmed-57422592018-01-08 Modulation of Intestinal Microbiome Prevents Intestinal Ischemic Injury Bertacco, Alessandra Dehner, Carina A. Caturegli, Giorgio D'Amico, Francesco Morotti, Raffaella Rodriguez, Manuel I. Mulligan, David C. Kriegel, Martin A. Geibel, John P. Front Physiol Physiology Background: Butyrate protects against ischemic injury to the small intestine by reducing inflammation and maintaining the structure of the intestinal barrier, but is expensive, short-lived, and cannot be administered easily due to its odor. Lactate, both economical and more palatable, can be converted into butyrate by the intestinal microbiome. This study aimed to assess in a rat model whether lactate perfusion can also protect against intestinal ischemia. Materials and Methods: Rat intestinal segments were loaded in an in vitro bowel perfusion device, and water absorption or secretion was assessed based on fluorescence of FITC-inulin, a fluorescent marker bound to a biologically inert sugar. Change in FITC concentration was used as a measure of ischemic injury, given the tendency of ischemic cells to retain water. Hematoxylin and eosin-stained sections at light level microscopy were examined to evaluate intestinal epithelium morphology. Comparisons between the data sets were paired Student t-tests or ANOVA with p < 0.05 performed on GraphPad. Results: Lactate administration resulted in a protective effect against intestinal ischemia of similar magnitude to that observed with butyrate. Both exhibited approximately 1.5 times the secretion exhibited by control sections (p = 0.03). Perfusion with lactate and methoxyacetate, a specific inhibitor of lactate-butyrate conversion, abolished this effect (p = 0.09). Antibiotic treatment also eliminated this effect, rendering lactate-perfused sections similar to control sections (p = 0.72). Perfusion with butyrate and methoxyacetate did not eliminate the observed increased secretion, which indicates that ischemic protection was mediated by microbial conversion of lactate to butyrate (p = 0.71). Conclusions: Lactate's protective effect against intestinal ischemia due to microbial conversion to butyrate suggests possible applications in the transplant setting for reducing ischemic injury and ameliorating intestinal preservation during transport. Frontiers Media S.A. 2017-12-19 /pmc/articles/PMC5742259/ /pubmed/29311987 http://dx.doi.org/10.3389/fphys.2017.01064 Text en Copyright © 2017 Bertacco, Dehner, Caturegli, D'Amico, Morotti, Rodriguez, Mulligan, Kriegel and Geibel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Bertacco, Alessandra
Dehner, Carina A.
Caturegli, Giorgio
D'Amico, Francesco
Morotti, Raffaella
Rodriguez, Manuel I.
Mulligan, David C.
Kriegel, Martin A.
Geibel, John P.
Modulation of Intestinal Microbiome Prevents Intestinal Ischemic Injury
title Modulation of Intestinal Microbiome Prevents Intestinal Ischemic Injury
title_full Modulation of Intestinal Microbiome Prevents Intestinal Ischemic Injury
title_fullStr Modulation of Intestinal Microbiome Prevents Intestinal Ischemic Injury
title_full_unstemmed Modulation of Intestinal Microbiome Prevents Intestinal Ischemic Injury
title_short Modulation of Intestinal Microbiome Prevents Intestinal Ischemic Injury
title_sort modulation of intestinal microbiome prevents intestinal ischemic injury
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742259/
https://www.ncbi.nlm.nih.gov/pubmed/29311987
http://dx.doi.org/10.3389/fphys.2017.01064
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