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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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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