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Effects of salvianolate on bone metabolism in glucocorticoid-treated lupus-prone B6.MRL-Fas(lpr)/J mice

AIM: To investigate the bone-protective effects of salvianolate (Sal), a total polyphenol from Radix Salviae miltiorrhizae, on bone tissue in the spontaneous lupus-prone mouse model, B6.MRL-Fas(lpr)/J, undergoing glucocorticoid (GC) treatment. METHODS: Fifteen-week-old female B6.MRL-Fas(lpr)/J mice...

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Autores principales: Liu, Yanzhi, Cui, Yang, Zhang, Xiao, Gao, Xiang, Su, Yanjie, Xu, Bilian, Wu, Tie, Chen, Wenshuang, Cui, Liao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4984994/
https://www.ncbi.nlm.nih.gov/pubmed/27563234
http://dx.doi.org/10.2147/DDDT.S110125
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author Liu, Yanzhi
Cui, Yang
Zhang, Xiao
Gao, Xiang
Su, Yanjie
Xu, Bilian
Wu, Tie
Chen, Wenshuang
Cui, Liao
author_facet Liu, Yanzhi
Cui, Yang
Zhang, Xiao
Gao, Xiang
Su, Yanjie
Xu, Bilian
Wu, Tie
Chen, Wenshuang
Cui, Liao
author_sort Liu, Yanzhi
collection PubMed
description AIM: To investigate the bone-protective effects of salvianolate (Sal), a total polyphenol from Radix Salviae miltiorrhizae, on bone tissue in the spontaneous lupus-prone mouse model, B6.MRL-Fas(lpr)/J, undergoing glucocorticoid (GC) treatment. METHODS: Fifteen-week-old female B6.MRL-Fas(lpr)/J mice were administered either a daily dose of saline (lupus group), prednisone 6 mg/kg (GC group), Sal 60 mg/kg (Sal group); or GC plus Sal (GC + Sal group) for a duration of 12 weeks. Age-matched female C57BL/6J wild-type (WT) mice were used for control. Micro-computed tomography assessments, bone histomorphometry analysis, bone biomechanical test, immunohistochemistry and immunoblotting analysis for bone markers, and renal histology analysis were performed to support our research endeavor. RESULTS: Lupus mice developed a marked bone loss and deterioration of mechanical properties of bone due to an increase in bone resorption rather than suppression of bone formation. GC treatment strongly inhibited bone formation in lupus mice. Sal treatment significantly attenuated osteogenic inhibition, and also suppressed hyperactive bone resorption, which recovered the bone mass and mechanical properties of bone in both the untreated and GC-treated lupus mice. CONCLUSION: The data support further preclinical investigation of Sal as a potential therapeutic strategy for the treatment of systemic lupus erythematosus-related bone loss.
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spelling pubmed-49849942016-08-25 Effects of salvianolate on bone metabolism in glucocorticoid-treated lupus-prone B6.MRL-Fas(lpr)/J mice Liu, Yanzhi Cui, Yang Zhang, Xiao Gao, Xiang Su, Yanjie Xu, Bilian Wu, Tie Chen, Wenshuang Cui, Liao Drug Des Devel Ther Original Research AIM: To investigate the bone-protective effects of salvianolate (Sal), a total polyphenol from Radix Salviae miltiorrhizae, on bone tissue in the spontaneous lupus-prone mouse model, B6.MRL-Fas(lpr)/J, undergoing glucocorticoid (GC) treatment. METHODS: Fifteen-week-old female B6.MRL-Fas(lpr)/J mice were administered either a daily dose of saline (lupus group), prednisone 6 mg/kg (GC group), Sal 60 mg/kg (Sal group); or GC plus Sal (GC + Sal group) for a duration of 12 weeks. Age-matched female C57BL/6J wild-type (WT) mice were used for control. Micro-computed tomography assessments, bone histomorphometry analysis, bone biomechanical test, immunohistochemistry and immunoblotting analysis for bone markers, and renal histology analysis were performed to support our research endeavor. RESULTS: Lupus mice developed a marked bone loss and deterioration of mechanical properties of bone due to an increase in bone resorption rather than suppression of bone formation. GC treatment strongly inhibited bone formation in lupus mice. Sal treatment significantly attenuated osteogenic inhibition, and also suppressed hyperactive bone resorption, which recovered the bone mass and mechanical properties of bone in both the untreated and GC-treated lupus mice. CONCLUSION: The data support further preclinical investigation of Sal as a potential therapeutic strategy for the treatment of systemic lupus erythematosus-related bone loss. Dove Medical Press 2016-08-09 /pmc/articles/PMC4984994/ /pubmed/27563234 http://dx.doi.org/10.2147/DDDT.S110125 Text en © 2016 Liu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Liu, Yanzhi
Cui, Yang
Zhang, Xiao
Gao, Xiang
Su, Yanjie
Xu, Bilian
Wu, Tie
Chen, Wenshuang
Cui, Liao
Effects of salvianolate on bone metabolism in glucocorticoid-treated lupus-prone B6.MRL-Fas(lpr)/J mice
title Effects of salvianolate on bone metabolism in glucocorticoid-treated lupus-prone B6.MRL-Fas(lpr)/J mice
title_full Effects of salvianolate on bone metabolism in glucocorticoid-treated lupus-prone B6.MRL-Fas(lpr)/J mice
title_fullStr Effects of salvianolate on bone metabolism in glucocorticoid-treated lupus-prone B6.MRL-Fas(lpr)/J mice
title_full_unstemmed Effects of salvianolate on bone metabolism in glucocorticoid-treated lupus-prone B6.MRL-Fas(lpr)/J mice
title_short Effects of salvianolate on bone metabolism in glucocorticoid-treated lupus-prone B6.MRL-Fas(lpr)/J mice
title_sort effects of salvianolate on bone metabolism in glucocorticoid-treated lupus-prone b6.mrl-fas(lpr)/j mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4984994/
https://www.ncbi.nlm.nih.gov/pubmed/27563234
http://dx.doi.org/10.2147/DDDT.S110125
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