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Changes in white adipose tissue metabolism induced by resveratrol in rats

BACKGROUND: A remarkable range of biological functions have been ascribed to resveratrol. Recently, this polyphenol has been shown to have body fat lowering effects. The aim of the present study was to assess some of the potential underlying mechanisms of action which take place in adipose tissue. M...

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Autores principales: Alberdi, Goiuri, Rodríguez, Víctor M, Miranda, Jonatan, Macarulla, María T, Arias, Noemí, Andrés-Lacueva, Cristina, Portillo, María P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101135/
https://www.ncbi.nlm.nih.gov/pubmed/21569266
http://dx.doi.org/10.1186/1743-7075-8-29
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author Alberdi, Goiuri
Rodríguez, Víctor M
Miranda, Jonatan
Macarulla, María T
Arias, Noemí
Andrés-Lacueva, Cristina
Portillo, María P
author_facet Alberdi, Goiuri
Rodríguez, Víctor M
Miranda, Jonatan
Macarulla, María T
Arias, Noemí
Andrés-Lacueva, Cristina
Portillo, María P
author_sort Alberdi, Goiuri
collection PubMed
description BACKGROUND: A remarkable range of biological functions have been ascribed to resveratrol. Recently, this polyphenol has been shown to have body fat lowering effects. The aim of the present study was to assess some of the potential underlying mechanisms of action which take place in adipose tissue. METHODS: Sixteen male Sprague-Dawley rats were randomly divided into two groups: control and treated with 30 mg resveratrol/kg body weight/d. All rats were fed an obesogenic diet and after six weeks of treatment white adipose tissues were dissected. Lipoprotein lipase activity was assessed by fluorimetry, acetyl-CoA carboxylase by radiometry, and malic enzyme, glucose-6P-dehydrogenase and fatty acid synthase by spectrophotometry. Gene expression levels of acetyl-CoA carboxylase, fatty acid synthase, lipoprotein lipase, hormone-sensitive lipase, adipose triglyceride lipase, PPAR-gamma, SREBP-1c and perilipin were assessed by Real time RT-PCR. The amount of resveratrol metabolites in adipose tissue was measured by chromatography. RESULTS: There was no difference in the final body weight of the rats; however, adipose tissues were significantly decreased in the resveratrol-treated group. Resveratrol reduced the activity of lipogenic enzymes, as well as that of heparin-releasable lipoprotein lipase. Moreover, a significant reduction was induced by this polyphenol in hormone-sensitive lipase mRNA levels. No significant changes were observed in other genes. Total amount of resveratrol metabolites in adipose tissue was 2.66 ± 0.55 nmol/g tissue. CONCLUSIONS: It can be proposed that the body fat-lowering effect of resveratrol is mediated, at least in part, by a reduction in fatty acid uptake from circulating triacylglycerols and also in de novo lipogenesis.
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spelling pubmed-31011352011-05-25 Changes in white adipose tissue metabolism induced by resveratrol in rats Alberdi, Goiuri Rodríguez, Víctor M Miranda, Jonatan Macarulla, María T Arias, Noemí Andrés-Lacueva, Cristina Portillo, María P Nutr Metab (Lond) Research BACKGROUND: A remarkable range of biological functions have been ascribed to resveratrol. Recently, this polyphenol has been shown to have body fat lowering effects. The aim of the present study was to assess some of the potential underlying mechanisms of action which take place in adipose tissue. METHODS: Sixteen male Sprague-Dawley rats were randomly divided into two groups: control and treated with 30 mg resveratrol/kg body weight/d. All rats were fed an obesogenic diet and after six weeks of treatment white adipose tissues were dissected. Lipoprotein lipase activity was assessed by fluorimetry, acetyl-CoA carboxylase by radiometry, and malic enzyme, glucose-6P-dehydrogenase and fatty acid synthase by spectrophotometry. Gene expression levels of acetyl-CoA carboxylase, fatty acid synthase, lipoprotein lipase, hormone-sensitive lipase, adipose triglyceride lipase, PPAR-gamma, SREBP-1c and perilipin were assessed by Real time RT-PCR. The amount of resveratrol metabolites in adipose tissue was measured by chromatography. RESULTS: There was no difference in the final body weight of the rats; however, adipose tissues were significantly decreased in the resveratrol-treated group. Resveratrol reduced the activity of lipogenic enzymes, as well as that of heparin-releasable lipoprotein lipase. Moreover, a significant reduction was induced by this polyphenol in hormone-sensitive lipase mRNA levels. No significant changes were observed in other genes. Total amount of resveratrol metabolites in adipose tissue was 2.66 ± 0.55 nmol/g tissue. CONCLUSIONS: It can be proposed that the body fat-lowering effect of resveratrol is mediated, at least in part, by a reduction in fatty acid uptake from circulating triacylglycerols and also in de novo lipogenesis. BioMed Central 2011-05-10 /pmc/articles/PMC3101135/ /pubmed/21569266 http://dx.doi.org/10.1186/1743-7075-8-29 Text en Copyright ©2011 Alberdi 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 Research
Alberdi, Goiuri
Rodríguez, Víctor M
Miranda, Jonatan
Macarulla, María T
Arias, Noemí
Andrés-Lacueva, Cristina
Portillo, María P
Changes in white adipose tissue metabolism induced by resveratrol in rats
title Changes in white adipose tissue metabolism induced by resveratrol in rats
title_full Changes in white adipose tissue metabolism induced by resveratrol in rats
title_fullStr Changes in white adipose tissue metabolism induced by resveratrol in rats
title_full_unstemmed Changes in white adipose tissue metabolism induced by resveratrol in rats
title_short Changes in white adipose tissue metabolism induced by resveratrol in rats
title_sort changes in white adipose tissue metabolism induced by resveratrol in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101135/
https://www.ncbi.nlm.nih.gov/pubmed/21569266
http://dx.doi.org/10.1186/1743-7075-8-29
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