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The inhibition of fat cell proliferation by n-3 fatty acids in dietary obese mice

BACKGROUND: Long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFA) of marine origin exert multiple beneficial effects on health. Our previous study in mice showed that reduction of adiposity by LC n-3 PUFA was associated with both, a shift in adipose tissue metabolism and a decrease in tissue cell...

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Autores principales: Hensler, Michal, Bardova, Kristina, Jilkova, Zuzana Macek, Wahli, Walter, Meztger, Daniel, Chambon, Pierre, Kopecky, Jan, Flachs, Pavel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162548/
https://www.ncbi.nlm.nih.gov/pubmed/21810216
http://dx.doi.org/10.1186/1476-511X-10-128
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author Hensler, Michal
Bardova, Kristina
Jilkova, Zuzana Macek
Wahli, Walter
Meztger, Daniel
Chambon, Pierre
Kopecky, Jan
Flachs, Pavel
author_facet Hensler, Michal
Bardova, Kristina
Jilkova, Zuzana Macek
Wahli, Walter
Meztger, Daniel
Chambon, Pierre
Kopecky, Jan
Flachs, Pavel
author_sort Hensler, Michal
collection PubMed
description BACKGROUND: Long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFA) of marine origin exert multiple beneficial effects on health. Our previous study in mice showed that reduction of adiposity by LC n-3 PUFA was associated with both, a shift in adipose tissue metabolism and a decrease in tissue cellularity. The aim of this study was to further characterize the effects of LC n-3 PUFA on fat cell proliferation and differentiation in obese mice. METHODS: A model of inducible and reversible lipoatrophy (aP2-Cre-ER(T2 )PPARγ(L2/L2 )mice) was used, in which the death of mature adipocytes could be achieved by a selective ablation of peroxisome proliferator-activated receptor γ in response to i.p. injection of tamoxifen. Before the injection, obesity was induced in male mice by 8-week-feeding a corn oil-based high-fat diet (cHF) and, subsequently, mice were randomly assigned (day 0) to one of the following groups: (i) mice injected by corn-oil-vehicle only, i.e."control" mice, and fed cHF; (ii) mice injected by tamoxifen in corn oil, i.e. "mutant" mice, fed cHF; (iii) control mice fed cHF diet with15% of dietary lipids replaced by LC n-3 PUFA concentrate (cHF+F); and (iv) mutant mice fed cHF+F. Blood and tissue samples were collected at days 14 and 42. RESULTS: Mutant mice achieved a maximum weight loss within 10 days post-injection, followed by a compensatory body weight gain, which was significantly faster in the cHF as compared with the cHF+F mutant mice. Also in control mice, body weight gain was depressed in response to dietary LC n-3 PUFA. At day 42, body weights in all groups stabilized, with no significant differences in adipocyte size between the groups, although body weight and adiposity was lower in the cHF+F as compared with the cHF mice, with a stronger effect in the mutant than in control mice. Gene expression analysis documented depression of adipocyte maturation during the reconstitution of adipose tissue in the cHF+F mutant mice. CONCLUSION: Dietary LC n-3 PUFA could reduce both hypertrophy and hyperplasia of fat cells in vivo. Results are in agreement with the involvement of fat cell turnover in control of adiposity.
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spelling pubmed-31625482011-08-27 The inhibition of fat cell proliferation by n-3 fatty acids in dietary obese mice Hensler, Michal Bardova, Kristina Jilkova, Zuzana Macek Wahli, Walter Meztger, Daniel Chambon, Pierre Kopecky, Jan Flachs, Pavel Lipids Health Dis Short Report BACKGROUND: Long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFA) of marine origin exert multiple beneficial effects on health. Our previous study in mice showed that reduction of adiposity by LC n-3 PUFA was associated with both, a shift in adipose tissue metabolism and a decrease in tissue cellularity. The aim of this study was to further characterize the effects of LC n-3 PUFA on fat cell proliferation and differentiation in obese mice. METHODS: A model of inducible and reversible lipoatrophy (aP2-Cre-ER(T2 )PPARγ(L2/L2 )mice) was used, in which the death of mature adipocytes could be achieved by a selective ablation of peroxisome proliferator-activated receptor γ in response to i.p. injection of tamoxifen. Before the injection, obesity was induced in male mice by 8-week-feeding a corn oil-based high-fat diet (cHF) and, subsequently, mice were randomly assigned (day 0) to one of the following groups: (i) mice injected by corn-oil-vehicle only, i.e."control" mice, and fed cHF; (ii) mice injected by tamoxifen in corn oil, i.e. "mutant" mice, fed cHF; (iii) control mice fed cHF diet with15% of dietary lipids replaced by LC n-3 PUFA concentrate (cHF+F); and (iv) mutant mice fed cHF+F. Blood and tissue samples were collected at days 14 and 42. RESULTS: Mutant mice achieved a maximum weight loss within 10 days post-injection, followed by a compensatory body weight gain, which was significantly faster in the cHF as compared with the cHF+F mutant mice. Also in control mice, body weight gain was depressed in response to dietary LC n-3 PUFA. At day 42, body weights in all groups stabilized, with no significant differences in adipocyte size between the groups, although body weight and adiposity was lower in the cHF+F as compared with the cHF mice, with a stronger effect in the mutant than in control mice. Gene expression analysis documented depression of adipocyte maturation during the reconstitution of adipose tissue in the cHF+F mutant mice. CONCLUSION: Dietary LC n-3 PUFA could reduce both hypertrophy and hyperplasia of fat cells in vivo. Results are in agreement with the involvement of fat cell turnover in control of adiposity. BioMed Central 2011-08-02 /pmc/articles/PMC3162548/ /pubmed/21810216 http://dx.doi.org/10.1186/1476-511X-10-128 Text en Copyright ©2011 Hensler et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Hensler, Michal
Bardova, Kristina
Jilkova, Zuzana Macek
Wahli, Walter
Meztger, Daniel
Chambon, Pierre
Kopecky, Jan
Flachs, Pavel
The inhibition of fat cell proliferation by n-3 fatty acids in dietary obese mice
title The inhibition of fat cell proliferation by n-3 fatty acids in dietary obese mice
title_full The inhibition of fat cell proliferation by n-3 fatty acids in dietary obese mice
title_fullStr The inhibition of fat cell proliferation by n-3 fatty acids in dietary obese mice
title_full_unstemmed The inhibition of fat cell proliferation by n-3 fatty acids in dietary obese mice
title_short The inhibition of fat cell proliferation by n-3 fatty acids in dietary obese mice
title_sort inhibition of fat cell proliferation by n-3 fatty acids in dietary obese mice
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162548/
https://www.ncbi.nlm.nih.gov/pubmed/21810216
http://dx.doi.org/10.1186/1476-511X-10-128
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