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Total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis

BACKGROUND: Total glucosides of paeony (TGP) is a biologically active compound extracted from Paeony root. TGP has been used in rheumatoid arthritis therapy for many years. However, the mechanism by which TGP prevents bone loss has been less explored. METHODS: TGP was orally administered for 3 month...

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Autores principales: Wei, Chen Chao, You, Fan Tian, Mei, Li Yu, Jian, Sun, Qiang, Chen Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728075/
https://www.ncbi.nlm.nih.gov/pubmed/23870279
http://dx.doi.org/10.1186/1472-6882-13-186
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author Wei, Chen Chao
You, Fan Tian
Mei, Li Yu
Jian, Sun
Qiang, Chen Yong
author_facet Wei, Chen Chao
You, Fan Tian
Mei, Li Yu
Jian, Sun
Qiang, Chen Yong
author_sort Wei, Chen Chao
collection PubMed
description BACKGROUND: Total glucosides of paeony (TGP) is a biologically active compound extracted from Paeony root. TGP has been used in rheumatoid arthritis therapy for many years. However, the mechanism by which TGP prevents bone loss has been less explored. METHODS: TGP was orally administered for 3 months to New Zealand rabbits with antigen-induced arthritis (AIA). Digital x-ray knee images and bone mineral density (BMD) measurements of the subchondral knee bone were performed before sacrifice. Chondrocytes were observed using transmission electron microscopy (TEM). Histological analysis and mRNA expression of receptor activator of nuclear factor-B ligand (RANKL) and osteoprotegerin (OPG) were evaluated in joint tissues. RESULTS: The BMD value in TGP rabbits was significantly higher compared with that seen in the AIA model rabbits. In addition, the subchondral bone plate was almost completely preserved by TGP treatment, while there was a decrease in bone plate integrity in AIA rabbits. There was less damage to the chondrocytes of the TGP treated group. Immunohistochemical examination of the TGP group showed that a higher percentage of TGP treated chondrocytes expressed OPG as compared to the chondrocytes isolated from AIA treated animals. In contrast, RANKL expression was significantly decreased in the TGP treated group compared to the AIA group. In support of the immunohistochemistry data, the expression of RANKL mRNA was decreased and OPG mRNA expression was enhanced in the TGP group when compared to that of the AIA model group. CONCLUSION: These results reveal that TGP suppresses juxta-articular osteoporosis and prevents subchondral bone loss. The decreased RANKL and increased OPG expression seen in TGP treated animals could explain how administration of TGP maintains higher BMD.
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spelling pubmed-37280752013-07-31 Total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis Wei, Chen Chao You, Fan Tian Mei, Li Yu Jian, Sun Qiang, Chen Yong BMC Complement Altern Med Research Article BACKGROUND: Total glucosides of paeony (TGP) is a biologically active compound extracted from Paeony root. TGP has been used in rheumatoid arthritis therapy for many years. However, the mechanism by which TGP prevents bone loss has been less explored. METHODS: TGP was orally administered for 3 months to New Zealand rabbits with antigen-induced arthritis (AIA). Digital x-ray knee images and bone mineral density (BMD) measurements of the subchondral knee bone were performed before sacrifice. Chondrocytes were observed using transmission electron microscopy (TEM). Histological analysis and mRNA expression of receptor activator of nuclear factor-B ligand (RANKL) and osteoprotegerin (OPG) were evaluated in joint tissues. RESULTS: The BMD value in TGP rabbits was significantly higher compared with that seen in the AIA model rabbits. In addition, the subchondral bone plate was almost completely preserved by TGP treatment, while there was a decrease in bone plate integrity in AIA rabbits. There was less damage to the chondrocytes of the TGP treated group. Immunohistochemical examination of the TGP group showed that a higher percentage of TGP treated chondrocytes expressed OPG as compared to the chondrocytes isolated from AIA treated animals. In contrast, RANKL expression was significantly decreased in the TGP treated group compared to the AIA group. In support of the immunohistochemistry data, the expression of RANKL mRNA was decreased and OPG mRNA expression was enhanced in the TGP group when compared to that of the AIA model group. CONCLUSION: These results reveal that TGP suppresses juxta-articular osteoporosis and prevents subchondral bone loss. The decreased RANKL and increased OPG expression seen in TGP treated animals could explain how administration of TGP maintains higher BMD. BioMed Central 2013-07-21 /pmc/articles/PMC3728075/ /pubmed/23870279 http://dx.doi.org/10.1186/1472-6882-13-186 Text en Copyright © 2013 Chao Wei et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wei, Chen Chao
You, Fan Tian
Mei, Li Yu
Jian, Sun
Qiang, Chen Yong
Total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis
title Total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis
title_full Total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis
title_fullStr Total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis
title_full_unstemmed Total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis
title_short Total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis
title_sort total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728075/
https://www.ncbi.nlm.nih.gov/pubmed/23870279
http://dx.doi.org/10.1186/1472-6882-13-186
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