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2-O-digalloyl-1,3,4,6-tetra-O-galloyl-β-D-glucose isolated from Galla Rhois suppresses osteoclast differentiation and function by inhibiting NF-κB signaling
Natural compounds isolated from medicinal herbs and plants have immense significance in maintaining bone health. Hydrolysable tannins have been shown to possess a variety of medicinal properties including antiviral, anticancer, and anti-osteoclastogenic activities. As a part of a study on the discov...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Biochemistry and Molecular Biology
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6605525/ https://www.ncbi.nlm.nih.gov/pubmed/31068248 http://dx.doi.org/10.5483/BMBRep.2019.52.6.063 |
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author | Ihn, Hye Jung Kim, Tae Hoon Kim, Kiryeong Kim, Gi-Young Jeon, You-Jin Choi, Yung Hyun Bae, Jong-Sup Kim, Jung-Eun Park, Eui Kyun |
author_facet | Ihn, Hye Jung Kim, Tae Hoon Kim, Kiryeong Kim, Gi-Young Jeon, You-Jin Choi, Yung Hyun Bae, Jong-Sup Kim, Jung-Eun Park, Eui Kyun |
author_sort | Ihn, Hye Jung |
collection | PubMed |
description | Natural compounds isolated from medicinal herbs and plants have immense significance in maintaining bone health. Hydrolysable tannins have been shown to possess a variety of medicinal properties including antiviral, anticancer, and anti-osteoclastogenic activities. As a part of a study on the discovery of alternative agent against skeletal diseases, we isolated a hydrolysable tannin, 2-O-digalloyl-1,3,4,6-tetra-O-galloyl- β-D-glucose (DTOGG), from Galla Rhois and examined the effect on osteoclast formation and function. We found that DTOGG significantly inhibited receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclast differentiation by downregulating the expression of the key regulator in osteoclastogenesis as well as osteoclast-related genes. Analysis of RANKL/RANK signaling revealed that DTOGG impaired activation of IκBα and p65 in the nuclear factor kappa-light-chain- enhancer of activated B cells (NF-κB) signaling pathway. Furthermore, DTOGG reduced bone resorbing activity of osteoclasts, compared to the vehicle-treated control. These results suggest that DTOGG could be a useful natural compound to manage osteoclast-mediated skeletal diseases. |
format | Online Article Text |
id | pubmed-6605525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-66055252019-07-10 2-O-digalloyl-1,3,4,6-tetra-O-galloyl-β-D-glucose isolated from Galla Rhois suppresses osteoclast differentiation and function by inhibiting NF-κB signaling Ihn, Hye Jung Kim, Tae Hoon Kim, Kiryeong Kim, Gi-Young Jeon, You-Jin Choi, Yung Hyun Bae, Jong-Sup Kim, Jung-Eun Park, Eui Kyun BMB Rep Reports Natural compounds isolated from medicinal herbs and plants have immense significance in maintaining bone health. Hydrolysable tannins have been shown to possess a variety of medicinal properties including antiviral, anticancer, and anti-osteoclastogenic activities. As a part of a study on the discovery of alternative agent against skeletal diseases, we isolated a hydrolysable tannin, 2-O-digalloyl-1,3,4,6-tetra-O-galloyl- β-D-glucose (DTOGG), from Galla Rhois and examined the effect on osteoclast formation and function. We found that DTOGG significantly inhibited receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclast differentiation by downregulating the expression of the key regulator in osteoclastogenesis as well as osteoclast-related genes. Analysis of RANKL/RANK signaling revealed that DTOGG impaired activation of IκBα and p65 in the nuclear factor kappa-light-chain- enhancer of activated B cells (NF-κB) signaling pathway. Furthermore, DTOGG reduced bone resorbing activity of osteoclasts, compared to the vehicle-treated control. These results suggest that DTOGG could be a useful natural compound to manage osteoclast-mediated skeletal diseases. Korean Society for Biochemistry and Molecular Biology 2019-06 2019-06-30 /pmc/articles/PMC6605525/ /pubmed/31068248 http://dx.doi.org/10.5483/BMBRep.2019.52.6.063 Text en Copyright © 2019 by the The Korean Society for Biochemistry and Molecular Biology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reports Ihn, Hye Jung Kim, Tae Hoon Kim, Kiryeong Kim, Gi-Young Jeon, You-Jin Choi, Yung Hyun Bae, Jong-Sup Kim, Jung-Eun Park, Eui Kyun 2-O-digalloyl-1,3,4,6-tetra-O-galloyl-β-D-glucose isolated from Galla Rhois suppresses osteoclast differentiation and function by inhibiting NF-κB signaling |
title | 2-O-digalloyl-1,3,4,6-tetra-O-galloyl-β-D-glucose isolated from Galla Rhois suppresses osteoclast differentiation and function by inhibiting NF-κB signaling |
title_full | 2-O-digalloyl-1,3,4,6-tetra-O-galloyl-β-D-glucose isolated from Galla Rhois suppresses osteoclast differentiation and function by inhibiting NF-κB signaling |
title_fullStr | 2-O-digalloyl-1,3,4,6-tetra-O-galloyl-β-D-glucose isolated from Galla Rhois suppresses osteoclast differentiation and function by inhibiting NF-κB signaling |
title_full_unstemmed | 2-O-digalloyl-1,3,4,6-tetra-O-galloyl-β-D-glucose isolated from Galla Rhois suppresses osteoclast differentiation and function by inhibiting NF-κB signaling |
title_short | 2-O-digalloyl-1,3,4,6-tetra-O-galloyl-β-D-glucose isolated from Galla Rhois suppresses osteoclast differentiation and function by inhibiting NF-κB signaling |
title_sort | 2-o-digalloyl-1,3,4,6-tetra-o-galloyl-β-d-glucose isolated from galla rhois suppresses osteoclast differentiation and function by inhibiting nf-κb signaling |
topic | Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6605525/ https://www.ncbi.nlm.nih.gov/pubmed/31068248 http://dx.doi.org/10.5483/BMBRep.2019.52.6.063 |
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