Cargando…

High intensity interval training promotes total and visceral fat mass loss in obese Zucker rats without modulating gut microbiota

AIMS: Increased visceral adipose tissue and dysbiosis in the overweight and obese promote chronic inflammation. The aim of this study was to compare the effects of moderate-intensity continuous training (MICT) and high-intensity interval training (HIIT) on the gut-adipose tissue cross-talk in obese...

Descripción completa

Detalles Bibliográficos
Autores principales: Maillard, Florie, Vazeille, Emilie, Sauvanet, Pierre, Sirvent, Pascal, Combaret, Lydie, Sourdrille, Antoine, Chavanelle, Vivien, Bonnet, Richard, Otero, Yolanda Fernandez, Delcros, Geoffrey, Barnich, Nicolas, Boisseau, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456220/
https://www.ncbi.nlm.nih.gov/pubmed/30964881
http://dx.doi.org/10.1371/journal.pone.0214660
_version_ 1783409733860851712
author Maillard, Florie
Vazeille, Emilie
Sauvanet, Pierre
Sirvent, Pascal
Combaret, Lydie
Sourdrille, Antoine
Chavanelle, Vivien
Bonnet, Richard
Otero, Yolanda Fernandez
Delcros, Geoffrey
Barnich, Nicolas
Boisseau, Nathalie
author_facet Maillard, Florie
Vazeille, Emilie
Sauvanet, Pierre
Sirvent, Pascal
Combaret, Lydie
Sourdrille, Antoine
Chavanelle, Vivien
Bonnet, Richard
Otero, Yolanda Fernandez
Delcros, Geoffrey
Barnich, Nicolas
Boisseau, Nathalie
author_sort Maillard, Florie
collection PubMed
description AIMS: Increased visceral adipose tissue and dysbiosis in the overweight and obese promote chronic inflammation. The aim of this study was to compare the effects of moderate-intensity continuous training (MICT) and high-intensity interval training (HIIT) on the gut-adipose tissue cross-talk in obese Zucker rats. METHODS: Obese male Zucker rats (n = 36) were divided in three groups: MICT (12m.min(-1) for 51min), HIIT (6 sets at 18 m.min(-1) for 4min followed by 3min at 10m.min(-1)) and controls (CONT; no exercise). The animals ran on a treadmill 5 days/week for 10 weeks. Body composition, glycaemic control, lipid profile, inflammation, lipolysis signalling in subcutaneous and visceral adipose tissue, intestinal permeability (tight junctions and plasma lipopolysaccharide binding protein; LBP), and gut microbiota composition were assessed in the three groups. RESULTS: After 10 weeks of exercise, total and epididymal fat mass decreased only in the HIIT group. The α/β adrenergic receptor RNA ratio in subcutaneous adipose tissue increased only in the HIIT group. The expression level of phosphorylated hormone-sensitive lipase was not modified by training. Both HIIT and MICT decreased inflammation (plasma myeloperoxidase and keratinocyte-derived chemokine secretion in adipose tissue) and improved glucose metabolism. Zonula occludens-1 and occludin were upregulated in the HIIT group. Plasma LBP was similarly reduced in both training groups. HIIT and MICT did not affect gut microbiota composition. CONCLUSION: In obese Zucker rats, HIIT and MICT improved inflammation and glucose metabolism. In contrast, only HIIT decreased total and visceral fat mass. These adaptations were not associated with modifications in gut microbiota composition.
format Online
Article
Text
id pubmed-6456220
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-64562202019-05-03 High intensity interval training promotes total and visceral fat mass loss in obese Zucker rats without modulating gut microbiota Maillard, Florie Vazeille, Emilie Sauvanet, Pierre Sirvent, Pascal Combaret, Lydie Sourdrille, Antoine Chavanelle, Vivien Bonnet, Richard Otero, Yolanda Fernandez Delcros, Geoffrey Barnich, Nicolas Boisseau, Nathalie PLoS One Research Article AIMS: Increased visceral adipose tissue and dysbiosis in the overweight and obese promote chronic inflammation. The aim of this study was to compare the effects of moderate-intensity continuous training (MICT) and high-intensity interval training (HIIT) on the gut-adipose tissue cross-talk in obese Zucker rats. METHODS: Obese male Zucker rats (n = 36) were divided in three groups: MICT (12m.min(-1) for 51min), HIIT (6 sets at 18 m.min(-1) for 4min followed by 3min at 10m.min(-1)) and controls (CONT; no exercise). The animals ran on a treadmill 5 days/week for 10 weeks. Body composition, glycaemic control, lipid profile, inflammation, lipolysis signalling in subcutaneous and visceral adipose tissue, intestinal permeability (tight junctions and plasma lipopolysaccharide binding protein; LBP), and gut microbiota composition were assessed in the three groups. RESULTS: After 10 weeks of exercise, total and epididymal fat mass decreased only in the HIIT group. The α/β adrenergic receptor RNA ratio in subcutaneous adipose tissue increased only in the HIIT group. The expression level of phosphorylated hormone-sensitive lipase was not modified by training. Both HIIT and MICT decreased inflammation (plasma myeloperoxidase and keratinocyte-derived chemokine secretion in adipose tissue) and improved glucose metabolism. Zonula occludens-1 and occludin were upregulated in the HIIT group. Plasma LBP was similarly reduced in both training groups. HIIT and MICT did not affect gut microbiota composition. CONCLUSION: In obese Zucker rats, HIIT and MICT improved inflammation and glucose metabolism. In contrast, only HIIT decreased total and visceral fat mass. These adaptations were not associated with modifications in gut microbiota composition. Public Library of Science 2019-04-09 /pmc/articles/PMC6456220/ /pubmed/30964881 http://dx.doi.org/10.1371/journal.pone.0214660 Text en © 2019 Maillard et al http://creativecommons.org/licenses/by/4.0/ This 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 the original author and source are credited.
spellingShingle Research Article
Maillard, Florie
Vazeille, Emilie
Sauvanet, Pierre
Sirvent, Pascal
Combaret, Lydie
Sourdrille, Antoine
Chavanelle, Vivien
Bonnet, Richard
Otero, Yolanda Fernandez
Delcros, Geoffrey
Barnich, Nicolas
Boisseau, Nathalie
High intensity interval training promotes total and visceral fat mass loss in obese Zucker rats without modulating gut microbiota
title High intensity interval training promotes total and visceral fat mass loss in obese Zucker rats without modulating gut microbiota
title_full High intensity interval training promotes total and visceral fat mass loss in obese Zucker rats without modulating gut microbiota
title_fullStr High intensity interval training promotes total and visceral fat mass loss in obese Zucker rats without modulating gut microbiota
title_full_unstemmed High intensity interval training promotes total and visceral fat mass loss in obese Zucker rats without modulating gut microbiota
title_short High intensity interval training promotes total and visceral fat mass loss in obese Zucker rats without modulating gut microbiota
title_sort high intensity interval training promotes total and visceral fat mass loss in obese zucker rats without modulating gut microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456220/
https://www.ncbi.nlm.nih.gov/pubmed/30964881
http://dx.doi.org/10.1371/journal.pone.0214660
work_keys_str_mv AT maillardflorie highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT vazeilleemilie highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT sauvanetpierre highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT sirventpascal highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT combaretlydie highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT sourdrilleantoine highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT chavanellevivien highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT bonnetrichard highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT oteroyolandafernandez highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT delcrosgeoffrey highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT barnichnicolas highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota
AT boisseaunathalie highintensityintervaltrainingpromotestotalandvisceralfatmasslossinobesezuckerratswithoutmodulatinggutmicrobiota