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Intestinal fatty acid-binding protein and gut permeability responses to exercise

PURPOSE: Intestinal cell damage due to physiological stressors (e.g. heat, oxidative, hypoperfusion/ischaemic) may contribute to increased intestinal permeability. The aim of this study was to assess changes in plasma intestinal fatty acid-binding protein (I-FABP) in response to exercise (with bovin...

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Autores principales: March, Daniel S., Marchbank, Tania, Playford, Raymond J., Jones, Arwel W., Thatcher, Rhys, Davison, Glen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388720/
https://www.ncbi.nlm.nih.gov/pubmed/28290057
http://dx.doi.org/10.1007/s00421-017-3582-4
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author March, Daniel S.
Marchbank, Tania
Playford, Raymond J.
Jones, Arwel W.
Thatcher, Rhys
Davison, Glen
author_facet March, Daniel S.
Marchbank, Tania
Playford, Raymond J.
Jones, Arwel W.
Thatcher, Rhys
Davison, Glen
author_sort March, Daniel S.
collection PubMed
description PURPOSE: Intestinal cell damage due to physiological stressors (e.g. heat, oxidative, hypoperfusion/ischaemic) may contribute to increased intestinal permeability. The aim of this study was to assess changes in plasma intestinal fatty acid-binding protein (I-FABP) in response to exercise (with bovine colostrum supplementation, Col, positive control) and compare this to intestinal barrier integrity/permeability (5 h urinary lactulose/rhamnose ratio, L/R). METHODS: In a double-blind, placebo-controlled, crossover design, 18 males completed two experimental arms (14 days of 20 g/day supplementation with Col or placebo, Plac). For each arm participants performed two baseline (resting) intestinal permeability assessments (L/R) pre-supplementation and one post-exercise following supplementation. Blood samples were collected pre- and post-exercise to determine I-FABP concentration. RESULTS: Two-way repeated measures ANOVA revealed an arm × time interaction for L/R and I-FABP (P < 0.001). Post hoc analyses showed urinary L/R increased post-exercise in Plac (273% of pre, P < 0.001) and Col (148% of pre, P < 0.001) with post-exercise values significantly lower with Col (P < 0.001). Plasma I-FABP increased post-exercise in Plac (191% of pre-exercise, P = 0.002) but not in the Col arm (107%, P = 0.862) with post-exercise values significantly lower with Col (P = 0.013). Correlations between the increase in I-FABP and L/R were evident for visit one (P = 0.044) but not visit two (P = 0.200) although overall plots/patterns do appear similar for each. CONCLUSION: These findings suggest that exercise-induced intestinal cellular damage/injury is partly implicated in changes in permeability but other factors must also contribute.
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spelling pubmed-53887202017-04-27 Intestinal fatty acid-binding protein and gut permeability responses to exercise March, Daniel S. Marchbank, Tania Playford, Raymond J. Jones, Arwel W. Thatcher, Rhys Davison, Glen Eur J Appl Physiol Original Article PURPOSE: Intestinal cell damage due to physiological stressors (e.g. heat, oxidative, hypoperfusion/ischaemic) may contribute to increased intestinal permeability. The aim of this study was to assess changes in plasma intestinal fatty acid-binding protein (I-FABP) in response to exercise (with bovine colostrum supplementation, Col, positive control) and compare this to intestinal barrier integrity/permeability (5 h urinary lactulose/rhamnose ratio, L/R). METHODS: In a double-blind, placebo-controlled, crossover design, 18 males completed two experimental arms (14 days of 20 g/day supplementation with Col or placebo, Plac). For each arm participants performed two baseline (resting) intestinal permeability assessments (L/R) pre-supplementation and one post-exercise following supplementation. Blood samples were collected pre- and post-exercise to determine I-FABP concentration. RESULTS: Two-way repeated measures ANOVA revealed an arm × time interaction for L/R and I-FABP (P < 0.001). Post hoc analyses showed urinary L/R increased post-exercise in Plac (273% of pre, P < 0.001) and Col (148% of pre, P < 0.001) with post-exercise values significantly lower with Col (P < 0.001). Plasma I-FABP increased post-exercise in Plac (191% of pre-exercise, P = 0.002) but not in the Col arm (107%, P = 0.862) with post-exercise values significantly lower with Col (P = 0.013). Correlations between the increase in I-FABP and L/R were evident for visit one (P = 0.044) but not visit two (P = 0.200) although overall plots/patterns do appear similar for each. CONCLUSION: These findings suggest that exercise-induced intestinal cellular damage/injury is partly implicated in changes in permeability but other factors must also contribute. Springer Berlin Heidelberg 2017-03-13 2017 /pmc/articles/PMC5388720/ /pubmed/28290057 http://dx.doi.org/10.1007/s00421-017-3582-4 Text en © The Author(s) 2017 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.
spellingShingle Original Article
March, Daniel S.
Marchbank, Tania
Playford, Raymond J.
Jones, Arwel W.
Thatcher, Rhys
Davison, Glen
Intestinal fatty acid-binding protein and gut permeability responses to exercise
title Intestinal fatty acid-binding protein and gut permeability responses to exercise
title_full Intestinal fatty acid-binding protein and gut permeability responses to exercise
title_fullStr Intestinal fatty acid-binding protein and gut permeability responses to exercise
title_full_unstemmed Intestinal fatty acid-binding protein and gut permeability responses to exercise
title_short Intestinal fatty acid-binding protein and gut permeability responses to exercise
title_sort intestinal fatty acid-binding protein and gut permeability responses to exercise
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388720/
https://www.ncbi.nlm.nih.gov/pubmed/28290057
http://dx.doi.org/10.1007/s00421-017-3582-4
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