author_facet Valli, Veronica
Heilmann, Katharina
Danesi, Francesca
Bordoni, Alessandra
Gerhäuser, Clarissa
Valli, Veronica
Heilmann, Katharina
Danesi, Francesca
Bordoni, Alessandra
Gerhäuser, Clarissa
author Valli, Veronica
Heilmann, Katharina
Danesi, Francesca
Bordoni, Alessandra
Gerhäuser, Clarissa
spellingShingle Valli, Veronica
Heilmann, Katharina
Danesi, Francesca
Bordoni, Alessandra
Gerhäuser, Clarissa
Oxidative Medicine and Cellular Longevity
Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
Cell Biology
Aging
General Medicine
Biochemistry
author_sort valli, veronica
spelling Valli, Veronica Heilmann, Katharina Danesi, Francesca Bordoni, Alessandra Gerhäuser, Clarissa 1942-0900 1942-0994 Hindawi Limited Cell Biology Aging General Medicine Biochemistry http://dx.doi.org/10.1155/2018/1617202 <jats:p>Obesity is characterized by excess body fat accumulation due to an increase in the size and number of differentiated mature adipocytes. Adipocyte differentiation is regulated by genetic and environmental factors, and its inhibition could represent a strategy for obesity prevention and treatment. The current study was designed with two aims: (i) to evaluate the changes in the expression of adipogenic markers (C/EBP<jats:italic>α</jats:italic>, PPAR<jats:italic>γ</jats:italic>variant 1 and variant 2, and GLUT4) in 3T3-L1 murine preadipocytes at four stages of the differentiation process and (ii) to compare the effectiveness of sulforaphane, genistein, and docosahexaenoic acid in reducing lipid accumulation and modulating C/EBP<jats:italic>α</jats:italic>, PPAR<jats:italic>γ</jats:italic>1, PPAR<jats:italic>γ</jats:italic>2, and GLUT4 mRNA expression in mature adipocytes. All bioactive compounds were shown to suppress adipocyte differentiation, although with different effectiveness. These results set the stage for further studies considering natural food constituents as important agents in preventing or treating obesity.</jats:p> Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity Oxidative Medicine and Cellular Longevity
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title Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_unstemmed Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_full Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_fullStr Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_full_unstemmed Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_short Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_sort modulation of adipocyte differentiation and proadipogenic gene expression by sulforaphane, genistein, and docosahexaenoic acid as a first step to counteract obesity
topic Cell Biology
Aging
General Medicine
Biochemistry
url http://dx.doi.org/10.1155/2018/1617202
publishDate 2018
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description <jats:p>Obesity is characterized by excess body fat accumulation due to an increase in the size and number of differentiated mature adipocytes. Adipocyte differentiation is regulated by genetic and environmental factors, and its inhibition could represent a strategy for obesity prevention and treatment. The current study was designed with two aims: (i) to evaluate the changes in the expression of adipogenic markers (C/EBP<jats:italic>α</jats:italic>, PPAR<jats:italic>γ</jats:italic>variant 1 and variant 2, and GLUT4) in 3T3-L1 murine preadipocytes at four stages of the differentiation process and (ii) to compare the effectiveness of sulforaphane, genistein, and docosahexaenoic acid in reducing lipid accumulation and modulating C/EBP<jats:italic>α</jats:italic>, PPAR<jats:italic>γ</jats:italic>1, PPAR<jats:italic>γ</jats:italic>2, and GLUT4 mRNA expression in mature adipocytes. All bioactive compounds were shown to suppress adipocyte differentiation, although with different effectiveness. These results set the stage for further studies considering natural food constituents as important agents in preventing or treating obesity.</jats:p>
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author Valli, Veronica, Heilmann, Katharina, Danesi, Francesca, Bordoni, Alessandra, Gerhäuser, Clarissa
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spelling Valli, Veronica Heilmann, Katharina Danesi, Francesca Bordoni, Alessandra Gerhäuser, Clarissa 1942-0900 1942-0994 Hindawi Limited Cell Biology Aging General Medicine Biochemistry http://dx.doi.org/10.1155/2018/1617202 <jats:p>Obesity is characterized by excess body fat accumulation due to an increase in the size and number of differentiated mature adipocytes. Adipocyte differentiation is regulated by genetic and environmental factors, and its inhibition could represent a strategy for obesity prevention and treatment. The current study was designed with two aims: (i) to evaluate the changes in the expression of adipogenic markers (C/EBP<jats:italic>α</jats:italic>, PPAR<jats:italic>γ</jats:italic>variant 1 and variant 2, and GLUT4) in 3T3-L1 murine preadipocytes at four stages of the differentiation process and (ii) to compare the effectiveness of sulforaphane, genistein, and docosahexaenoic acid in reducing lipid accumulation and modulating C/EBP<jats:italic>α</jats:italic>, PPAR<jats:italic>γ</jats:italic>1, PPAR<jats:italic>γ</jats:italic>2, and GLUT4 mRNA expression in mature adipocytes. All bioactive compounds were shown to suppress adipocyte differentiation, although with different effectiveness. These results set the stage for further studies considering natural food constituents as important agents in preventing or treating obesity.</jats:p> Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity Oxidative Medicine and Cellular Longevity
spellingShingle Valli, Veronica, Heilmann, Katharina, Danesi, Francesca, Bordoni, Alessandra, Gerhäuser, Clarissa, Oxidative Medicine and Cellular Longevity, Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity, Cell Biology, Aging, General Medicine, Biochemistry
title Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_full Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_fullStr Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_full_unstemmed Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_short Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
title_sort modulation of adipocyte differentiation and proadipogenic gene expression by sulforaphane, genistein, and docosahexaenoic acid as a first step to counteract obesity
title_unstemmed Modulation of Adipocyte Differentiation and Proadipogenic Gene Expression by Sulforaphane, Genistein, and Docosahexaenoic Acid as a First Step to Counteract Obesity
topic Cell Biology, Aging, General Medicine, Biochemistry
url http://dx.doi.org/10.1155/2018/1617202