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Polyphenols from Chilean Propolis and Pinocembrin Reduce MMP-9 Gene Expression and Activity in Activated Macrophages

Polyphenols from diverse sources have shown anti-inflammatory activity. In the context of atherosclerosis, macrophages play important roles including matrix metalloproteinases synthesis involved in degradation of matrix extracellular components affecting the atherosclerotic plaque stability. We prep...

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Autores principales: Saavedra, Nicolás, Cuevas, Alejandro, Cavalcante, Marcela F., Dörr, Felipe A., Saavedra, Kathleen, Zambrano, Tomás, Abdalla, Dulcineia S. P., Salazar, Luis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826909/
https://www.ncbi.nlm.nih.gov/pubmed/27119082
http://dx.doi.org/10.1155/2016/6505383
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author Saavedra, Nicolás
Cuevas, Alejandro
Cavalcante, Marcela F.
Dörr, Felipe A.
Saavedra, Kathleen
Zambrano, Tomás
Abdalla, Dulcineia S. P.
Salazar, Luis A.
author_facet Saavedra, Nicolás
Cuevas, Alejandro
Cavalcante, Marcela F.
Dörr, Felipe A.
Saavedra, Kathleen
Zambrano, Tomás
Abdalla, Dulcineia S. P.
Salazar, Luis A.
author_sort Saavedra, Nicolás
collection PubMed
description Polyphenols from diverse sources have shown anti-inflammatory activity. In the context of atherosclerosis, macrophages play important roles including matrix metalloproteinases synthesis involved in degradation of matrix extracellular components affecting the atherosclerotic plaque stability. We prepared a propolis extract and pinocembrin in ethanol solution. Propolis extract was chemically characterized using LC-MS. The effect of treatments on gene expression and proteolytic activity was measured in vitro using murine macrophages activated with LPS. Cellular toxicity associated with both treatments and the vehicle was determined using MTT and apoptosis/necrosis detection assays. MMP-9 gene expression and proteolytic activity were measured using qPCR and zymography, respectively. Thirty-two compounds were identified in the propolis extract, including pinocembrin among its major components. Treatment with either ethanolic extract of propolis or pinocembrin inhibits MMP-9 gene expression in a dose-dependent manner. Similarly, an inhibitory effect was observed in proteolytic activity. However, the effect showed by ethanolic extract of propolis was higher than the effect of pinocembrin, suggesting that MMP-9 inhibition results from a joint contribution between the components of the extract. These data suggest a potential role of polyphenols from Chilean propolis in the control of extracellular matrix degradation in atherosclerotic plaques.
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spelling pubmed-48269092016-04-26 Polyphenols from Chilean Propolis and Pinocembrin Reduce MMP-9 Gene Expression and Activity in Activated Macrophages Saavedra, Nicolás Cuevas, Alejandro Cavalcante, Marcela F. Dörr, Felipe A. Saavedra, Kathleen Zambrano, Tomás Abdalla, Dulcineia S. P. Salazar, Luis A. Biomed Res Int Research Article Polyphenols from diverse sources have shown anti-inflammatory activity. In the context of atherosclerosis, macrophages play important roles including matrix metalloproteinases synthesis involved in degradation of matrix extracellular components affecting the atherosclerotic plaque stability. We prepared a propolis extract and pinocembrin in ethanol solution. Propolis extract was chemically characterized using LC-MS. The effect of treatments on gene expression and proteolytic activity was measured in vitro using murine macrophages activated with LPS. Cellular toxicity associated with both treatments and the vehicle was determined using MTT and apoptosis/necrosis detection assays. MMP-9 gene expression and proteolytic activity were measured using qPCR and zymography, respectively. Thirty-two compounds were identified in the propolis extract, including pinocembrin among its major components. Treatment with either ethanolic extract of propolis or pinocembrin inhibits MMP-9 gene expression in a dose-dependent manner. Similarly, an inhibitory effect was observed in proteolytic activity. However, the effect showed by ethanolic extract of propolis was higher than the effect of pinocembrin, suggesting that MMP-9 inhibition results from a joint contribution between the components of the extract. These data suggest a potential role of polyphenols from Chilean propolis in the control of extracellular matrix degradation in atherosclerotic plaques. Hindawi Publishing Corporation 2016 2016-03-28 /pmc/articles/PMC4826909/ /pubmed/27119082 http://dx.doi.org/10.1155/2016/6505383 Text en Copyright © 2016 Nicolás Saavedra et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Saavedra, Nicolás
Cuevas, Alejandro
Cavalcante, Marcela F.
Dörr, Felipe A.
Saavedra, Kathleen
Zambrano, Tomás
Abdalla, Dulcineia S. P.
Salazar, Luis A.
Polyphenols from Chilean Propolis and Pinocembrin Reduce MMP-9 Gene Expression and Activity in Activated Macrophages
title Polyphenols from Chilean Propolis and Pinocembrin Reduce MMP-9 Gene Expression and Activity in Activated Macrophages
title_full Polyphenols from Chilean Propolis and Pinocembrin Reduce MMP-9 Gene Expression and Activity in Activated Macrophages
title_fullStr Polyphenols from Chilean Propolis and Pinocembrin Reduce MMP-9 Gene Expression and Activity in Activated Macrophages
title_full_unstemmed Polyphenols from Chilean Propolis and Pinocembrin Reduce MMP-9 Gene Expression and Activity in Activated Macrophages
title_short Polyphenols from Chilean Propolis and Pinocembrin Reduce MMP-9 Gene Expression and Activity in Activated Macrophages
title_sort polyphenols from chilean propolis and pinocembrin reduce mmp-9 gene expression and activity in activated macrophages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826909/
https://www.ncbi.nlm.nih.gov/pubmed/27119082
http://dx.doi.org/10.1155/2016/6505383
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