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Phenolic Compounds Inhibit 3T3-L1 Adipogenesis Depending on the Stage of Differentiation and Their Binding Affinity to PPARγ

Phenolic compounds might modulate adiposity. Here, we report our observation that polyphenols and phenolic acids inhibit adipogenesis in 3T3-L1 with different intensity depending on the family and the stage of differentiation. While quercetin and resveratrol inhibited lipid accumulation along the wh...

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Autores principales: Aranaz, Paula, Navarro-Herrera, David, Zabala, María, Miguéliz, Itziar, Romo-Hualde, Ana, López-Yoldi, Miguel, Martínez, J. Alfredo, Vizmanos, José Luis, Milagro, Fermín I., González-Navarro, Carlos Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470710/
https://www.ncbi.nlm.nih.gov/pubmed/30884812
http://dx.doi.org/10.3390/molecules24061045
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author Aranaz, Paula
Navarro-Herrera, David
Zabala, María
Miguéliz, Itziar
Romo-Hualde, Ana
López-Yoldi, Miguel
Martínez, J. Alfredo
Vizmanos, José Luis
Milagro, Fermín I.
González-Navarro, Carlos Javier
author_facet Aranaz, Paula
Navarro-Herrera, David
Zabala, María
Miguéliz, Itziar
Romo-Hualde, Ana
López-Yoldi, Miguel
Martínez, J. Alfredo
Vizmanos, José Luis
Milagro, Fermín I.
González-Navarro, Carlos Javier
author_sort Aranaz, Paula
collection PubMed
description Phenolic compounds might modulate adiposity. Here, we report our observation that polyphenols and phenolic acids inhibit adipogenesis in 3T3-L1 with different intensity depending on the family and the stage of differentiation. While quercetin and resveratrol inhibited lipid accumulation along the whole process of differentiation, apigenin and myricetin were active during the early and latest stages, but not intermediate, contrary to hesperidin. The activity of phenolic acids was limited to the early stages of the differentiation process, except p-coumaric and ellagic acids. This anti-adipogenic effect was accompanied by down-regulation of Scd1 and Lpl. Molecular docking analysis revealed that the inhibitory activity of these phenolic compounds over the early stages of adipogenesis exhibits a significant correlation (r = 0.7034; p = 0.005) with their binding affinity to the ligand-binding domain of PPARγ. Results show that polyphenols and phenolic acids would interact with specific residues of the receptor, which could determine their potential anti-adipogenic activity during the early stages of the differentiation. Residues Phe264, His266, Ile281, Cys285 and Met348 are the most frequently involved in these interactions, which might suggest a crucial role for these amino acids modulating the activity of the receptor. These data contribute to elucidate the possible mechanisms of phenolic compounds in the control of adipogenesis.
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spelling pubmed-64707102019-04-26 Phenolic Compounds Inhibit 3T3-L1 Adipogenesis Depending on the Stage of Differentiation and Their Binding Affinity to PPARγ Aranaz, Paula Navarro-Herrera, David Zabala, María Miguéliz, Itziar Romo-Hualde, Ana López-Yoldi, Miguel Martínez, J. Alfredo Vizmanos, José Luis Milagro, Fermín I. González-Navarro, Carlos Javier Molecules Article Phenolic compounds might modulate adiposity. Here, we report our observation that polyphenols and phenolic acids inhibit adipogenesis in 3T3-L1 with different intensity depending on the family and the stage of differentiation. While quercetin and resveratrol inhibited lipid accumulation along the whole process of differentiation, apigenin and myricetin were active during the early and latest stages, but not intermediate, contrary to hesperidin. The activity of phenolic acids was limited to the early stages of the differentiation process, except p-coumaric and ellagic acids. This anti-adipogenic effect was accompanied by down-regulation of Scd1 and Lpl. Molecular docking analysis revealed that the inhibitory activity of these phenolic compounds over the early stages of adipogenesis exhibits a significant correlation (r = 0.7034; p = 0.005) with their binding affinity to the ligand-binding domain of PPARγ. Results show that polyphenols and phenolic acids would interact with specific residues of the receptor, which could determine their potential anti-adipogenic activity during the early stages of the differentiation. Residues Phe264, His266, Ile281, Cys285 and Met348 are the most frequently involved in these interactions, which might suggest a crucial role for these amino acids modulating the activity of the receptor. These data contribute to elucidate the possible mechanisms of phenolic compounds in the control of adipogenesis. MDPI 2019-03-16 /pmc/articles/PMC6470710/ /pubmed/30884812 http://dx.doi.org/10.3390/molecules24061045 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aranaz, Paula
Navarro-Herrera, David
Zabala, María
Miguéliz, Itziar
Romo-Hualde, Ana
López-Yoldi, Miguel
Martínez, J. Alfredo
Vizmanos, José Luis
Milagro, Fermín I.
González-Navarro, Carlos Javier
Phenolic Compounds Inhibit 3T3-L1 Adipogenesis Depending on the Stage of Differentiation and Their Binding Affinity to PPARγ
title Phenolic Compounds Inhibit 3T3-L1 Adipogenesis Depending on the Stage of Differentiation and Their Binding Affinity to PPARγ
title_full Phenolic Compounds Inhibit 3T3-L1 Adipogenesis Depending on the Stage of Differentiation and Their Binding Affinity to PPARγ
title_fullStr Phenolic Compounds Inhibit 3T3-L1 Adipogenesis Depending on the Stage of Differentiation and Their Binding Affinity to PPARγ
title_full_unstemmed Phenolic Compounds Inhibit 3T3-L1 Adipogenesis Depending on the Stage of Differentiation and Their Binding Affinity to PPARγ
title_short Phenolic Compounds Inhibit 3T3-L1 Adipogenesis Depending on the Stage of Differentiation and Their Binding Affinity to PPARγ
title_sort phenolic compounds inhibit 3t3-l1 adipogenesis depending on the stage of differentiation and their binding affinity to pparγ
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470710/
https://www.ncbi.nlm.nih.gov/pubmed/30884812
http://dx.doi.org/10.3390/molecules24061045
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