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Tridax procumbens flavonoids promote osteoblast differentiation and bone formation

BACKGROUND: Tridax procumbens flavonoids (TPFs) are well known for their medicinal properties among local natives. Besides traditionally used for dropsy, anemia, arthritis, gout, asthma, ulcer, piles, and urinary problems, it is also used in treating gastric problems, body pain, and rheumatic pains...

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Autores principales: Al Mamun, Md. Abdullah, Hosen, Mohammad Jakir, Islam, Kamrul, Khatun, Amina, Alam, M. Masihul, Al-Bari, Md. Abdul Alim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652438/
https://www.ncbi.nlm.nih.gov/pubmed/26581452
http://dx.doi.org/10.1186/s40659-015-0056-1
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author Al Mamun, Md. Abdullah
Hosen, Mohammad Jakir
Islam, Kamrul
Khatun, Amina
Alam, M. Masihul
Al-Bari, Md. Abdul Alim
author_facet Al Mamun, Md. Abdullah
Hosen, Mohammad Jakir
Islam, Kamrul
Khatun, Amina
Alam, M. Masihul
Al-Bari, Md. Abdul Alim
author_sort Al Mamun, Md. Abdullah
collection PubMed
description BACKGROUND: Tridax procumbens flavonoids (TPFs) are well known for their medicinal properties among local natives. Besides traditionally used for dropsy, anemia, arthritis, gout, asthma, ulcer, piles, and urinary problems, it is also used in treating gastric problems, body pain, and rheumatic pains of joints. TPFs have been reported to increase osteogenic functioning in mesenchymal stem cells. Our previous study showed that TPFs were significantly suppressed the RANKL-induced differentiation of osteoclasts and bone resorption. However, the effects of TPFs to promote osteoblasts differentiation and bone formation remain unclear. TPFs were isolated from Tridax procumbens and investigated for their effects on osteoblasts differentiation and bone formation by using primary mouse calvarial osteoblasts. RESULTS: TPFs promoted osteoblast differentiation in a dose-dependent manner demonstrated by up-regulation of alkaline phosphatase and osteocalcin. TPFs also upregulated osteoblast differentiation related genes, including osteocalcin, osterix, and Runx2 in primary osteoblasts. TPFs treated primary osteoblast cells showed significant upregulation of bone morphogenetic proteins (BMPs) including Bmp-2, Bmp-4, and Bmp-7. Addition of noggin, a BMP specific-antagonist, inhibited TPFs induced upregulation of the osteocalcin, osterix, and Runx2. CONCLUSION: Our findings point towards the induction of osteoblast differentiation by TPFs and suggested that TPFs could be a potential anabolic agent to treat patients with bone loss-associated diseases such as osteoporosis.
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spelling pubmed-46524382015-11-20 Tridax procumbens flavonoids promote osteoblast differentiation and bone formation Al Mamun, Md. Abdullah Hosen, Mohammad Jakir Islam, Kamrul Khatun, Amina Alam, M. Masihul Al-Bari, Md. Abdul Alim Biol Res Research Article BACKGROUND: Tridax procumbens flavonoids (TPFs) are well known for their medicinal properties among local natives. Besides traditionally used for dropsy, anemia, arthritis, gout, asthma, ulcer, piles, and urinary problems, it is also used in treating gastric problems, body pain, and rheumatic pains of joints. TPFs have been reported to increase osteogenic functioning in mesenchymal stem cells. Our previous study showed that TPFs were significantly suppressed the RANKL-induced differentiation of osteoclasts and bone resorption. However, the effects of TPFs to promote osteoblasts differentiation and bone formation remain unclear. TPFs were isolated from Tridax procumbens and investigated for their effects on osteoblasts differentiation and bone formation by using primary mouse calvarial osteoblasts. RESULTS: TPFs promoted osteoblast differentiation in a dose-dependent manner demonstrated by up-regulation of alkaline phosphatase and osteocalcin. TPFs also upregulated osteoblast differentiation related genes, including osteocalcin, osterix, and Runx2 in primary osteoblasts. TPFs treated primary osteoblast cells showed significant upregulation of bone morphogenetic proteins (BMPs) including Bmp-2, Bmp-4, and Bmp-7. Addition of noggin, a BMP specific-antagonist, inhibited TPFs induced upregulation of the osteocalcin, osterix, and Runx2. CONCLUSION: Our findings point towards the induction of osteoblast differentiation by TPFs and suggested that TPFs could be a potential anabolic agent to treat patients with bone loss-associated diseases such as osteoporosis. BioMed Central 2015-11-18 /pmc/articles/PMC4652438/ /pubmed/26581452 http://dx.doi.org/10.1186/s40659-015-0056-1 Text en © Al Mamun et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Al Mamun, Md. Abdullah
Hosen, Mohammad Jakir
Islam, Kamrul
Khatun, Amina
Alam, M. Masihul
Al-Bari, Md. Abdul Alim
Tridax procumbens flavonoids promote osteoblast differentiation and bone formation
title Tridax procumbens flavonoids promote osteoblast differentiation and bone formation
title_full Tridax procumbens flavonoids promote osteoblast differentiation and bone formation
title_fullStr Tridax procumbens flavonoids promote osteoblast differentiation and bone formation
title_full_unstemmed Tridax procumbens flavonoids promote osteoblast differentiation and bone formation
title_short Tridax procumbens flavonoids promote osteoblast differentiation and bone formation
title_sort tridax procumbens flavonoids promote osteoblast differentiation and bone formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652438/
https://www.ncbi.nlm.nih.gov/pubmed/26581452
http://dx.doi.org/10.1186/s40659-015-0056-1
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