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Effects of the antihypertensive drug benidipine on osteoblast function in vitro

The dihydropyridine-type calcium channel blocker, benidipine (BD) has been widely used in hypertension therapy. Previous studies have demonstrated that BD has a positive effect on bone metabolism. Inspired by this promoting phenomenon, the present study investigated the effects of BD on osteoblasts...

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Detalles Bibliográficos
Autores principales: WANG, BAIXIANG, BI, MING, ZHU, ZHEN, WU, LEI, WANG, JINGYUN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919856/
https://www.ncbi.nlm.nih.gov/pubmed/24520261
http://dx.doi.org/10.3892/etm.2014.1475
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author WANG, BAIXIANG
BI, MING
ZHU, ZHEN
WU, LEI
WANG, JINGYUN
author_facet WANG, BAIXIANG
BI, MING
ZHU, ZHEN
WU, LEI
WANG, JINGYUN
author_sort WANG, BAIXIANG
collection PubMed
description The dihydropyridine-type calcium channel blocker, benidipine (BD) has been widely used in hypertension therapy. Previous studies have demonstrated that BD has a positive effect on bone metabolism. Inspired by this promoting phenomenon, the present study investigated the effects of BD on osteoblasts in vitro. Experiments were designed and performed, including an MTT assay, reverse transcription-polymerase chain reaction, western blot analysis, alkaline phosphatase activity measurements and alizarin red S staining. The results demonstrated that BD promoted osteoblast proliferation and osteogenic differentiation at concentrations from 1×10(−6) to 1×10(−9) M by upregulating Runx2, BMP2 and OCN gene expression levels. Overall, BD at appropriate concentrations has been demonstrated to have positive effects on osteoblast function in addition to its conventional clinical usage.
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spelling pubmed-39198562014-02-11 Effects of the antihypertensive drug benidipine on osteoblast function in vitro WANG, BAIXIANG BI, MING ZHU, ZHEN WU, LEI WANG, JINGYUN Exp Ther Med Articles The dihydropyridine-type calcium channel blocker, benidipine (BD) has been widely used in hypertension therapy. Previous studies have demonstrated that BD has a positive effect on bone metabolism. Inspired by this promoting phenomenon, the present study investigated the effects of BD on osteoblasts in vitro. Experiments were designed and performed, including an MTT assay, reverse transcription-polymerase chain reaction, western blot analysis, alkaline phosphatase activity measurements and alizarin red S staining. The results demonstrated that BD promoted osteoblast proliferation and osteogenic differentiation at concentrations from 1×10(−6) to 1×10(−9) M by upregulating Runx2, BMP2 and OCN gene expression levels. Overall, BD at appropriate concentrations has been demonstrated to have positive effects on osteoblast function in addition to its conventional clinical usage. D.A. Spandidos 2014-03 2014-01-03 /pmc/articles/PMC3919856/ /pubmed/24520261 http://dx.doi.org/10.3892/etm.2014.1475 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
WANG, BAIXIANG
BI, MING
ZHU, ZHEN
WU, LEI
WANG, JINGYUN
Effects of the antihypertensive drug benidipine on osteoblast function in vitro
title Effects of the antihypertensive drug benidipine on osteoblast function in vitro
title_full Effects of the antihypertensive drug benidipine on osteoblast function in vitro
title_fullStr Effects of the antihypertensive drug benidipine on osteoblast function in vitro
title_full_unstemmed Effects of the antihypertensive drug benidipine on osteoblast function in vitro
title_short Effects of the antihypertensive drug benidipine on osteoblast function in vitro
title_sort effects of the antihypertensive drug benidipine on osteoblast function in vitro
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919856/
https://www.ncbi.nlm.nih.gov/pubmed/24520261
http://dx.doi.org/10.3892/etm.2014.1475
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