Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells

Vitexin (5,7,4-trihydroxyflavone-8-glucoside), a natural flavone present in a variety of plants, is well known for its rich pharmacological properties. However, its osteogenic activity remains unclear to date. The purpose of this study was to explore the effects of vitexin on osteogenic activity i...

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Main Authors: Yuan, Xiaohan, Han, Haiyan, Luo, Zhaohui, Wang, Qiuxue, Tang, Peijia, Zhang, Zhihui, Fu, Yujie, Gu, Chengbo
Format: Article
Language:English
Published: Penerbit Universiti Kebangsaan Malaysia 2020
Online Access:http://journalarticle.ukm.my/15474/
http://journalarticle.ukm.my/15474/1/17.pdf
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author Yuan, Xiaohan
Han, Haiyan
Luo, Zhaohui
Wang, Qiuxue
Tang, Peijia
Zhang, Zhihui
Fu, Yujie
Gu, Chengbo
author_facet Yuan, Xiaohan
Han, Haiyan
Luo, Zhaohui
Wang, Qiuxue
Tang, Peijia
Zhang, Zhihui
Fu, Yujie
Gu, Chengbo
author_sort Yuan, Xiaohan
building UKM Institutional Repository
collection Online Access
description Vitexin (5,7,4-trihydroxyflavone-8-glucoside), a natural flavone present in a variety of plants, is well known for its rich pharmacological properties. However, its osteogenic activity remains unclear to date. The purpose of this study was to explore the effects of vitexin on osteogenic activity in murine pre-osteoblastic MC3T3-E1 cells using the MTT assay for cell proliferation, alkaline phosphatase (ALP) activity assay for cell differentiation, and Von Kossa staining for cell mineralization. Quantitative real-time PCR was used for the detection of osteocalcin (OCN) mRNA expression in cells. Furthermore, effects of vitexin on the differentiation and matrix mineralization of dexamethasone (DEX)- suppressed cells was also investigated. The results showed vitexin could significantly enhance cell proliferation in a low concentration range of 10-10-10-6 μg mL-1. ALP activity was significantly increased after the cells were treated with vitexin at 10-8 and 10-6 μg mL-1. The expression levels of the osteogenic OCN gene in cells treated with vitexin at 10-6, 10- 8, and 10-10 μg mL-1 were improved by 3.1-fold, 5.8-fold, and 4.2-fold over the control, respectively. Additionally, vitexin (10-8 μg mL-1) significantly alleviated the inhibitory effect of osteoblast differentiation and mineralization induced by DEX. Collectively, our findings suggest vitexin could enhance cell proliferation and osteogenic differentiation of MC3T3-E1 cells, as well as rescue the inhibitory effect of cell differentiation and matrix mineralization induced by DEX. Therefore, vitexin may be useful as a promising therapeutic agent for bone disease and plays an important role in the prevention of glucocorticoid-induced osteoporosis.
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spelling oai:generic.eprints.org:154742020-10-30T04:52:29Z http://journalarticle.ukm.my/15474/ Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells Yuan, Xiaohan Han, Haiyan Luo, Zhaohui Wang, Qiuxue Tang, Peijia Zhang, Zhihui Fu, Yujie Gu, Chengbo Vitexin (5,7,4-trihydroxyflavone-8-glucoside), a natural flavone present in a variety of plants, is well known for its rich pharmacological properties. However, its osteogenic activity remains unclear to date. The purpose of this study was to explore the effects of vitexin on osteogenic activity in murine pre-osteoblastic MC3T3-E1 cells using the MTT assay for cell proliferation, alkaline phosphatase (ALP) activity assay for cell differentiation, and Von Kossa staining for cell mineralization. Quantitative real-time PCR was used for the detection of osteocalcin (OCN) mRNA expression in cells. Furthermore, effects of vitexin on the differentiation and matrix mineralization of dexamethasone (DEX)- suppressed cells was also investigated. The results showed vitexin could significantly enhance cell proliferation in a low concentration range of 10-10-10-6 μg mL-1. ALP activity was significantly increased after the cells were treated with vitexin at 10-8 and 10-6 μg mL-1. The expression levels of the osteogenic OCN gene in cells treated with vitexin at 10-6, 10- 8, and 10-10 μg mL-1 were improved by 3.1-fold, 5.8-fold, and 4.2-fold over the control, respectively. Additionally, vitexin (10-8 μg mL-1) significantly alleviated the inhibitory effect of osteoblast differentiation and mineralization induced by DEX. Collectively, our findings suggest vitexin could enhance cell proliferation and osteogenic differentiation of MC3T3-E1 cells, as well as rescue the inhibitory effect of cell differentiation and matrix mineralization induced by DEX. Therefore, vitexin may be useful as a promising therapeutic agent for bone disease and plays an important role in the prevention of glucocorticoid-induced osteoporosis. Penerbit Universiti Kebangsaan Malaysia 2020-06 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/15474/1/17.pdf Yuan, Xiaohan and Han, Haiyan and Luo, Zhaohui and Wang, Qiuxue and Tang, Peijia and Zhang, Zhihui and Fu, Yujie and Gu, Chengbo (2020) Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells. Sains Malaysiana, 49 (6). pp. 1389-1400. ISSN 0126-6039 http://www.ukm.my/jsm/malay_journals/jilid49bil6_2020/KandunganJilid49Bil6_2020.html
spellingShingle Yuan, Xiaohan
Han, Haiyan
Luo, Zhaohui
Wang, Qiuxue
Tang, Peijia
Zhang, Zhihui
Fu, Yujie
Gu, Chengbo
Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells
title Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells
title_full Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells
title_fullStr Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells
title_full_unstemmed Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells
title_short Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells
title_sort enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic mc3t3-e1 cells
url http://journalarticle.ukm.my/15474/
http://journalarticle.ukm.my/15474/
http://journalarticle.ukm.my/15474/1/17.pdf