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Formononetin, a Beer Polyphenol with Catabolic Effects on Chondrocytes
Beer consumption has been identified as a risk factor for osteoarthritis (OA), a rheumatic disease characterised by cartilage degradation, joint inflammation, and eventual joint failure. One of the main isoflavonoids in beer is formononetin (FNT), an estrogenic compound also found in multiple plants...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10346251/ https://www.ncbi.nlm.nih.gov/pubmed/37447284 http://dx.doi.org/10.3390/nu15132959 |
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author | Guillán-Fresco, María Franco-Trepat, Eloi Alonso-Pérez, Ana Jorge-Mora, Alberto López-López, Verónica Pazos-Pérez, Andrés Piñeiro-Ramil, María Gómez, Rodolfo |
author_facet | Guillán-Fresco, María Franco-Trepat, Eloi Alonso-Pérez, Ana Jorge-Mora, Alberto López-López, Verónica Pazos-Pérez, Andrés Piñeiro-Ramil, María Gómez, Rodolfo |
author_sort | Guillán-Fresco, María |
collection | PubMed |
description | Beer consumption has been identified as a risk factor for osteoarthritis (OA), a rheumatic disease characterised by cartilage degradation, joint inflammation, and eventual joint failure. One of the main isoflavonoids in beer is formononetin (FNT), an estrogenic compound also found in multiple plants and herbs. In this study, we aimed to investigate the effect of FNT on chondrocyte viability, inflammation, and metabolism. Cells were treated with FNT with or without IL-1β for 48 h and during 7 days of differentiation. Cell viability was determined via MTT assay. Nitrite accumulation was determined by Griess reaction. The expression of genes involved in inflammation and metabolism was determined by RT-PCR. The results revealed that a low concentration of FNT had no deleterious effect on cell viability and decreased the expression of inflammation-related genes. However, our results suggest that FNT overexposure negatively impacts on chondrocytes by promoting catabolic responses. Finally, these effects were not mediated by estrogen receptors (ERs) or aryl hydrocarbon receptor (AhR). In conclusion, factors that favour FNT accumulation, such as long exposure times or metabolic disorders, can promote chondrocyte catabolism. These data may partially explain why beer consumption increases the risk of OA. |
format | Online Article Text |
id | pubmed-10346251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103462512023-07-15 Formononetin, a Beer Polyphenol with Catabolic Effects on Chondrocytes Guillán-Fresco, María Franco-Trepat, Eloi Alonso-Pérez, Ana Jorge-Mora, Alberto López-López, Verónica Pazos-Pérez, Andrés Piñeiro-Ramil, María Gómez, Rodolfo Nutrients Article Beer consumption has been identified as a risk factor for osteoarthritis (OA), a rheumatic disease characterised by cartilage degradation, joint inflammation, and eventual joint failure. One of the main isoflavonoids in beer is formononetin (FNT), an estrogenic compound also found in multiple plants and herbs. In this study, we aimed to investigate the effect of FNT on chondrocyte viability, inflammation, and metabolism. Cells were treated with FNT with or without IL-1β for 48 h and during 7 days of differentiation. Cell viability was determined via MTT assay. Nitrite accumulation was determined by Griess reaction. The expression of genes involved in inflammation and metabolism was determined by RT-PCR. The results revealed that a low concentration of FNT had no deleterious effect on cell viability and decreased the expression of inflammation-related genes. However, our results suggest that FNT overexposure negatively impacts on chondrocytes by promoting catabolic responses. Finally, these effects were not mediated by estrogen receptors (ERs) or aryl hydrocarbon receptor (AhR). In conclusion, factors that favour FNT accumulation, such as long exposure times or metabolic disorders, can promote chondrocyte catabolism. These data may partially explain why beer consumption increases the risk of OA. MDPI 2023-06-29 /pmc/articles/PMC10346251/ /pubmed/37447284 http://dx.doi.org/10.3390/nu15132959 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Guillán-Fresco, María Franco-Trepat, Eloi Alonso-Pérez, Ana Jorge-Mora, Alberto López-López, Verónica Pazos-Pérez, Andrés Piñeiro-Ramil, María Gómez, Rodolfo Formononetin, a Beer Polyphenol with Catabolic Effects on Chondrocytes |
title | Formononetin, a Beer Polyphenol with Catabolic Effects on Chondrocytes |
title_full | Formononetin, a Beer Polyphenol with Catabolic Effects on Chondrocytes |
title_fullStr | Formononetin, a Beer Polyphenol with Catabolic Effects on Chondrocytes |
title_full_unstemmed | Formononetin, a Beer Polyphenol with Catabolic Effects on Chondrocytes |
title_short | Formononetin, a Beer Polyphenol with Catabolic Effects on Chondrocytes |
title_sort | formononetin, a beer polyphenol with catabolic effects on chondrocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10346251/ https://www.ncbi.nlm.nih.gov/pubmed/37447284 http://dx.doi.org/10.3390/nu15132959 |
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