Leucine supplementation protects from insulin resistance by regulating adiposity levels.

<h4>Background</h4>Leucine supplementation might have therapeutic potential in preventing diet-induced obesity and improving insulin sensitivity. However, the underlying mechanisms are at present unclear. Additionally, it is unclear whether leucine supplementation might be equally effica...

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Main Authors: Elke Binder, Francisco J Bermúdez-Silva, Caroline André, Melissa Elie, Silvana Y Romero-Zerbo, Thierry Leste-Lasserre, Ilaria Belluomo, Adeline Duchampt, Samantha Clark, Agnes Aubert, Marco Mezzullo, Flaminia Fanelli, Uberto Pagotto, Sophie Layé, Gilles Mithieux, Daniela Cota
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24086364/?tool=EBI
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spelling doaj-678caa2a0db24dd5b44b6883e71f65e12021-03-03T22:51:18ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7470510.1371/journal.pone.0074705Leucine supplementation protects from insulin resistance by regulating adiposity levels.Elke BinderFrancisco J Bermúdez-SilvaCaroline AndréMelissa ElieSilvana Y Romero-ZerboThierry Leste-LasserreIlaria BelluomoAdeline DuchamptSamantha ClarkAgnes AubertMarco MezzulloFlaminia FanelliUberto PagottoSophie LayéGilles MithieuxDaniela Cota<h4>Background</h4>Leucine supplementation might have therapeutic potential in preventing diet-induced obesity and improving insulin sensitivity. However, the underlying mechanisms are at present unclear. Additionally, it is unclear whether leucine supplementation might be equally efficacious once obesity has developed.<h4>Methodology/principal findings</h4>Male C57BL/6J mice were fed chow or a high-fat diet (HFD), supplemented or not with leucine for 17 weeks. Another group of HFD-fed mice (HFD-pairfat group) was food restricted in order to reach an adiposity level comparable to that of HFD-Leu mice. Finally, a third group of mice was exposed to HFD for 12 weeks before being chronically supplemented with leucine. Leucine supplementation in HFD-fed mice decreased body weight and fat mass by increasing energy expenditure, fatty acid oxidation and locomotor activity in vivo. The decreased adiposity in HFD-Leu mice was associated with increased expression of uncoupling protein 3 (UCP-3) in the brown adipose tissue, better insulin sensitivity, increased intestinal gluconeogenesis and preservation of islets of Langerhans histomorphology and function. HFD-pairfat mice had a comparable improvement in insulin sensitivity, without changes in islets physiology or intestinal gluconeogenesis. Remarkably, both HFD-Leu and HFD-pairfat mice had decreased hepatic lipid content, which likely helped improve insulin sensitivity. In contrast, when leucine was supplemented to already obese animals, no changes in body weight, body composition or glucose metabolism were observed.<h4>Conclusions/significance</h4>These findings suggest that leucine improves insulin sensitivity in HFD-fed mice by primarily decreasing adiposity, rather than directly acting on peripheral target organs. However, beneficial effects of leucine on intestinal gluconeogenesis and islets of Langerhans's physiology might help prevent type 2 diabetes development. Differently, metabolic benefit of leucine supplementation is lacking in already obese animals, a phenomenon possibly related to the extent of the obesity before starting the supplementation.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24086364/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Elke Binder
Francisco J Bermúdez-Silva
Caroline André
Melissa Elie
Silvana Y Romero-Zerbo
Thierry Leste-Lasserre
Ilaria Belluomo
Adeline Duchampt
Samantha Clark
Agnes Aubert
Marco Mezzullo
Flaminia Fanelli
Uberto Pagotto
Sophie Layé
Gilles Mithieux
Daniela Cota
spellingShingle Elke Binder
Francisco J Bermúdez-Silva
Caroline André
Melissa Elie
Silvana Y Romero-Zerbo
Thierry Leste-Lasserre
Ilaria Belluomo
Adeline Duchampt
Samantha Clark
Agnes Aubert
Marco Mezzullo
Flaminia Fanelli
Uberto Pagotto
Sophie Layé
Gilles Mithieux
Daniela Cota
Leucine supplementation protects from insulin resistance by regulating adiposity levels.
PLoS ONE
author_facet Elke Binder
Francisco J Bermúdez-Silva
Caroline André
Melissa Elie
Silvana Y Romero-Zerbo
Thierry Leste-Lasserre
Ilaria Belluomo
Adeline Duchampt
Samantha Clark
Agnes Aubert
Marco Mezzullo
Flaminia Fanelli
Uberto Pagotto
Sophie Layé
Gilles Mithieux
Daniela Cota
author_sort Elke Binder
title Leucine supplementation protects from insulin resistance by regulating adiposity levels.
title_short Leucine supplementation protects from insulin resistance by regulating adiposity levels.
title_full Leucine supplementation protects from insulin resistance by regulating adiposity levels.
title_fullStr Leucine supplementation protects from insulin resistance by regulating adiposity levels.
title_full_unstemmed Leucine supplementation protects from insulin resistance by regulating adiposity levels.
title_sort leucine supplementation protects from insulin resistance by regulating adiposity levels.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description <h4>Background</h4>Leucine supplementation might have therapeutic potential in preventing diet-induced obesity and improving insulin sensitivity. However, the underlying mechanisms are at present unclear. Additionally, it is unclear whether leucine supplementation might be equally efficacious once obesity has developed.<h4>Methodology/principal findings</h4>Male C57BL/6J mice were fed chow or a high-fat diet (HFD), supplemented or not with leucine for 17 weeks. Another group of HFD-fed mice (HFD-pairfat group) was food restricted in order to reach an adiposity level comparable to that of HFD-Leu mice. Finally, a third group of mice was exposed to HFD for 12 weeks before being chronically supplemented with leucine. Leucine supplementation in HFD-fed mice decreased body weight and fat mass by increasing energy expenditure, fatty acid oxidation and locomotor activity in vivo. The decreased adiposity in HFD-Leu mice was associated with increased expression of uncoupling protein 3 (UCP-3) in the brown adipose tissue, better insulin sensitivity, increased intestinal gluconeogenesis and preservation of islets of Langerhans histomorphology and function. HFD-pairfat mice had a comparable improvement in insulin sensitivity, without changes in islets physiology or intestinal gluconeogenesis. Remarkably, both HFD-Leu and HFD-pairfat mice had decreased hepatic lipid content, which likely helped improve insulin sensitivity. In contrast, when leucine was supplemented to already obese animals, no changes in body weight, body composition or glucose metabolism were observed.<h4>Conclusions/significance</h4>These findings suggest that leucine improves insulin sensitivity in HFD-fed mice by primarily decreasing adiposity, rather than directly acting on peripheral target organs. However, beneficial effects of leucine on intestinal gluconeogenesis and islets of Langerhans's physiology might help prevent type 2 diabetes development. Differently, metabolic benefit of leucine supplementation is lacking in already obese animals, a phenomenon possibly related to the extent of the obesity before starting the supplementation.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24086364/?tool=EBI
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