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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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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. |
format | Online Article Text |
id | pubmed-3162548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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