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Black and Green Tea as Well as Specialty Teas Increase Osteoblast Mineralization with Varying Effectiveness

Many human studies suggest a benefit of tea consumption on bone health. The study objective was to compare the ability of different tea types to promote mineralization. Saos-2 cells underwent mineralization (5 days) in the presence of tea (white: WT, green: GT, black: BT, green rooibos: GR, or red r...

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Autores principales: McAlpine, Michael D., Gittings, William, MacNeil, Adam J., Ward, Wendy E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403192/
https://www.ncbi.nlm.nih.gov/pubmed/33252307
http://dx.doi.org/10.1089/jmf.2020.0139
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author McAlpine, Michael D.
Gittings, William
MacNeil, Adam J.
Ward, Wendy E.
author_facet McAlpine, Michael D.
Gittings, William
MacNeil, Adam J.
Ward, Wendy E.
author_sort McAlpine, Michael D.
collection PubMed
description Many human studies suggest a benefit of tea consumption on bone health. The study objective was to compare the ability of different tea types to promote mineralization. Saos-2 cells underwent mineralization (5 days) in the presence of tea (white: WT, green: GT, black: BT, green rooibos: GR, or red rooibos: RR; 1 μg/mL of polyphenols) or control. Total polyphenol content (TPC, Folin-Ciocalteu's reagent), antioxidant capacity (2,2-diphenyl-1-picrylhydrazyl [DPPH] scavenging), mineralization (Alizarin Red staining), gene expression quantitative reverse transcription PCR (RT-qPCR), and cell activity (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide assay) were determined. TPC was highest in GT and BT. The ability of each tea to inhibit DPPH also differed (WT, GT > RR) after normalizing for polyphenol quantity. Each tea increased mineralization and differences were observed among types (GT/BT/GR/RR > WT, GT = BT = GR, RR > BT/GT). mRNA expression of alkaline phosphatase (ALP) and ectonucleotide pyrophosphatase/phosphodiesterase (NPP1) remained unchanged, whereas osteopontin (OPN) and sclerostin (SOST) were reduced in cells treated with tea, regardless of type. At 24- and 48-h postexposure to tea, cell activity was greater in cells receiving any of the teas compared with vehicle control. Supplementation increased mineralization regardless of tea type with both rooibos teas and black tea stimulating greater mineralization than WT, whereas green tea is similar to the others. While future study is needed to confirm in vivo effects, the results suggest that consuming any of the teas studied may benefit bone health.
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spelling pubmed-84031922021-08-30 Black and Green Tea as Well as Specialty Teas Increase Osteoblast Mineralization with Varying Effectiveness McAlpine, Michael D. Gittings, William MacNeil, Adam J. Ward, Wendy E. J Med Food Full Communications Many human studies suggest a benefit of tea consumption on bone health. The study objective was to compare the ability of different tea types to promote mineralization. Saos-2 cells underwent mineralization (5 days) in the presence of tea (white: WT, green: GT, black: BT, green rooibos: GR, or red rooibos: RR; 1 μg/mL of polyphenols) or control. Total polyphenol content (TPC, Folin-Ciocalteu's reagent), antioxidant capacity (2,2-diphenyl-1-picrylhydrazyl [DPPH] scavenging), mineralization (Alizarin Red staining), gene expression quantitative reverse transcription PCR (RT-qPCR), and cell activity (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide assay) were determined. TPC was highest in GT and BT. The ability of each tea to inhibit DPPH also differed (WT, GT > RR) after normalizing for polyphenol quantity. Each tea increased mineralization and differences were observed among types (GT/BT/GR/RR > WT, GT = BT = GR, RR > BT/GT). mRNA expression of alkaline phosphatase (ALP) and ectonucleotide pyrophosphatase/phosphodiesterase (NPP1) remained unchanged, whereas osteopontin (OPN) and sclerostin (SOST) were reduced in cells treated with tea, regardless of type. At 24- and 48-h postexposure to tea, cell activity was greater in cells receiving any of the teas compared with vehicle control. Supplementation increased mineralization regardless of tea type with both rooibos teas and black tea stimulating greater mineralization than WT, whereas green tea is similar to the others. While future study is needed to confirm in vivo effects, the results suggest that consuming any of the teas studied may benefit bone health. Mary Ann Liebert, Inc., publishers 2021-08-01 2021-08-17 /pmc/articles/PMC8403192/ /pubmed/33252307 http://dx.doi.org/10.1089/jmf.2020.0139 Text en © Michael D. McAlpine et al. 2021; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by/4.0/This Open Access article is distributed under the terms of the Creative Commons License [CC-BY] (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Communications
McAlpine, Michael D.
Gittings, William
MacNeil, Adam J.
Ward, Wendy E.
Black and Green Tea as Well as Specialty Teas Increase Osteoblast Mineralization with Varying Effectiveness
title Black and Green Tea as Well as Specialty Teas Increase Osteoblast Mineralization with Varying Effectiveness
title_full Black and Green Tea as Well as Specialty Teas Increase Osteoblast Mineralization with Varying Effectiveness
title_fullStr Black and Green Tea as Well as Specialty Teas Increase Osteoblast Mineralization with Varying Effectiveness
title_full_unstemmed Black and Green Tea as Well as Specialty Teas Increase Osteoblast Mineralization with Varying Effectiveness
title_short Black and Green Tea as Well as Specialty Teas Increase Osteoblast Mineralization with Varying Effectiveness
title_sort black and green tea as well as specialty teas increase osteoblast mineralization with varying effectiveness
topic Full Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403192/
https://www.ncbi.nlm.nih.gov/pubmed/33252307
http://dx.doi.org/10.1089/jmf.2020.0139
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