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Effects of bisphenol F, bisphenol S, and bisphenol AF on cultured human osteoblasts
Bisphenol A (BPA) analogs, like BPA, could have adverse effects on human health including bone health. The aim was to determine the effect of BPF, BPS and BPAF on the growth and differentiation of cultured human osteoblasts. Osteoblasts primary culture from bone chips harvested during routine dental...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256648/ https://www.ncbi.nlm.nih.gov/pubmed/37198449 http://dx.doi.org/10.1007/s00204-023-03523-2 |
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author | García-Recio, E. Costela-Ruiz, V. J. Melguizo-Rodríguez, L. Ramos-Torrecillas, J. Illescas-Montes, R. De Luna-Bertos, E. Ruiz, C. |
author_facet | García-Recio, E. Costela-Ruiz, V. J. Melguizo-Rodríguez, L. Ramos-Torrecillas, J. Illescas-Montes, R. De Luna-Bertos, E. Ruiz, C. |
author_sort | García-Recio, E. |
collection | PubMed |
description | Bisphenol A (BPA) analogs, like BPA, could have adverse effects on human health including bone health. The aim was to determine the effect of BPF, BPS and BPAF on the growth and differentiation of cultured human osteoblasts. Osteoblasts primary culture from bone chips harvested during routine dental work and treated with BPF, BPS, or BPAF for 24 h at doses of 10(–5), 10(–6), and 10(–7) M. Next, cell proliferation was studied, apoptosis induction, and alkaline phosphatase (ALP) activity. In addition, mineralization was evaluated at 7, 14, and 21 days of cell culture in an osteogenic medium supplemented with BP analog at the studied doses. BPS treatment inhibited proliferation in a dose-dependent manner at all three doses by inducing apoptosis; BPF exerted a significant inhibitory effect on cell proliferation at the highest dose alone by an increase of apoptosis; while BPAF had no effect on proliferation or cell viability. Cell differentiation was adversely affected by treatment with BPA analogs in a dose-dependent, observing a reduction in calcium nodule formation at 21 days. According to the results obtained, these BPA analogs could potentially pose a threat to bone health, depending on their concentration in the organism. |
format | Online Article Text |
id | pubmed-10256648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-102566482023-06-11 Effects of bisphenol F, bisphenol S, and bisphenol AF on cultured human osteoblasts García-Recio, E. Costela-Ruiz, V. J. Melguizo-Rodríguez, L. Ramos-Torrecillas, J. Illescas-Montes, R. De Luna-Bertos, E. Ruiz, C. Arch Toxicol In Vitro Systems Bisphenol A (BPA) analogs, like BPA, could have adverse effects on human health including bone health. The aim was to determine the effect of BPF, BPS and BPAF on the growth and differentiation of cultured human osteoblasts. Osteoblasts primary culture from bone chips harvested during routine dental work and treated with BPF, BPS, or BPAF for 24 h at doses of 10(–5), 10(–6), and 10(–7) M. Next, cell proliferation was studied, apoptosis induction, and alkaline phosphatase (ALP) activity. In addition, mineralization was evaluated at 7, 14, and 21 days of cell culture in an osteogenic medium supplemented with BP analog at the studied doses. BPS treatment inhibited proliferation in a dose-dependent manner at all three doses by inducing apoptosis; BPF exerted a significant inhibitory effect on cell proliferation at the highest dose alone by an increase of apoptosis; while BPAF had no effect on proliferation or cell viability. Cell differentiation was adversely affected by treatment with BPA analogs in a dose-dependent, observing a reduction in calcium nodule formation at 21 days. According to the results obtained, these BPA analogs could potentially pose a threat to bone health, depending on their concentration in the organism. Springer Berlin Heidelberg 2023-05-17 2023 /pmc/articles/PMC10256648/ /pubmed/37198449 http://dx.doi.org/10.1007/s00204-023-03523-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | In Vitro Systems García-Recio, E. Costela-Ruiz, V. J. Melguizo-Rodríguez, L. Ramos-Torrecillas, J. Illescas-Montes, R. De Luna-Bertos, E. Ruiz, C. Effects of bisphenol F, bisphenol S, and bisphenol AF on cultured human osteoblasts |
title | Effects of bisphenol F, bisphenol S, and bisphenol AF on cultured human osteoblasts |
title_full | Effects of bisphenol F, bisphenol S, and bisphenol AF on cultured human osteoblasts |
title_fullStr | Effects of bisphenol F, bisphenol S, and bisphenol AF on cultured human osteoblasts |
title_full_unstemmed | Effects of bisphenol F, bisphenol S, and bisphenol AF on cultured human osteoblasts |
title_short | Effects of bisphenol F, bisphenol S, and bisphenol AF on cultured human osteoblasts |
title_sort | effects of bisphenol f, bisphenol s, and bisphenol af on cultured human osteoblasts |
topic | In Vitro Systems |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256648/ https://www.ncbi.nlm.nih.gov/pubmed/37198449 http://dx.doi.org/10.1007/s00204-023-03523-2 |
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