Cargando…
Effect of Salicornia herbacea on Osteoblastogenesis and Adipogenesis in Vitro
Bone-related complications are among the highest concerning metabolic diseases in the modern world. Bone fragility and susceptibility to fracture increase with age and diseases like osteoporosis. Elevated adipogenesis in bone results in osteoporosis and loss of bone mass when coupled with lack of os...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210889/ https://www.ncbi.nlm.nih.gov/pubmed/25310765 http://dx.doi.org/10.3390/md12105132 |
_version_ | 1782341466070188032 |
---|---|
author | Karadeniz, Fatih Kim, Jung-Ae Ahn, Byul-Nim Kwon, Myeong Sook Kong, Chang-Suk |
author_facet | Karadeniz, Fatih Kim, Jung-Ae Ahn, Byul-Nim Kwon, Myeong Sook Kong, Chang-Suk |
author_sort | Karadeniz, Fatih |
collection | PubMed |
description | Bone-related complications are among the highest concerning metabolic diseases in the modern world. Bone fragility and susceptibility to fracture increase with age and diseases like osteoporosis. Elevated adipogenesis in bone results in osteoporosis and loss of bone mass when coupled with lack of osteoblastogenesis. In this study the potential effect of Salicornia herbacea extract against osteoporotic conditions was evaluated. Adipogenesis inhibitory effect of S. herbacea has been evidenced by decreased lipid accumulation of differentiating cells and expression levels of crucial adipogenesis markers in 3T3-L1 pre-adipocytes. S. herbacea treatment reduced the lipid accumulation by 25% of the control. In addition, mRNA expression of peroxisome proliferator-activated receptor (PPAR)γ, CCAAT/enhancer-binding protein (C/EBP)α and sterol regulatory element binding protein (SREBP)1c were inhibited by the presence of S. herbacea. Bone formation enhancement effect of S. herbacea was also confirmed in MC3T3-E1 pre-osteoblasts. The presence of S. herbacea significantly elevated the alkaline phosphatase (ALP) activity by 120% at a concentration of 100 μg/mL in differentiating osteoblasts. S. herbacea also significantly increased the expression of osteoblastogenesis indicators, ALP, bone morphogenetic protein (BMP)-2, osteocalcin and collagen type I (collagen-I). In conclusion, S. herbacea possess potential to be utilized as a source of anti-osteoporotic agent that can inhibit adipogenesis while promoting osteoblastogenesis. |
format | Online Article Text |
id | pubmed-4210889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-42108892014-10-28 Effect of Salicornia herbacea on Osteoblastogenesis and Adipogenesis in Vitro Karadeniz, Fatih Kim, Jung-Ae Ahn, Byul-Nim Kwon, Myeong Sook Kong, Chang-Suk Mar Drugs Article Bone-related complications are among the highest concerning metabolic diseases in the modern world. Bone fragility and susceptibility to fracture increase with age and diseases like osteoporosis. Elevated adipogenesis in bone results in osteoporosis and loss of bone mass when coupled with lack of osteoblastogenesis. In this study the potential effect of Salicornia herbacea extract against osteoporotic conditions was evaluated. Adipogenesis inhibitory effect of S. herbacea has been evidenced by decreased lipid accumulation of differentiating cells and expression levels of crucial adipogenesis markers in 3T3-L1 pre-adipocytes. S. herbacea treatment reduced the lipid accumulation by 25% of the control. In addition, mRNA expression of peroxisome proliferator-activated receptor (PPAR)γ, CCAAT/enhancer-binding protein (C/EBP)α and sterol regulatory element binding protein (SREBP)1c were inhibited by the presence of S. herbacea. Bone formation enhancement effect of S. herbacea was also confirmed in MC3T3-E1 pre-osteoblasts. The presence of S. herbacea significantly elevated the alkaline phosphatase (ALP) activity by 120% at a concentration of 100 μg/mL in differentiating osteoblasts. S. herbacea also significantly increased the expression of osteoblastogenesis indicators, ALP, bone morphogenetic protein (BMP)-2, osteocalcin and collagen type I (collagen-I). In conclusion, S. herbacea possess potential to be utilized as a source of anti-osteoporotic agent that can inhibit adipogenesis while promoting osteoblastogenesis. MDPI 2014-10-10 /pmc/articles/PMC4210889/ /pubmed/25310765 http://dx.doi.org/10.3390/md12105132 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Karadeniz, Fatih Kim, Jung-Ae Ahn, Byul-Nim Kwon, Myeong Sook Kong, Chang-Suk Effect of Salicornia herbacea on Osteoblastogenesis and Adipogenesis in Vitro |
title | Effect of Salicornia herbacea on Osteoblastogenesis and Adipogenesis in Vitro |
title_full | Effect of Salicornia herbacea on Osteoblastogenesis and Adipogenesis in Vitro |
title_fullStr | Effect of Salicornia herbacea on Osteoblastogenesis and Adipogenesis in Vitro |
title_full_unstemmed | Effect of Salicornia herbacea on Osteoblastogenesis and Adipogenesis in Vitro |
title_short | Effect of Salicornia herbacea on Osteoblastogenesis and Adipogenesis in Vitro |
title_sort | effect of salicornia herbacea on osteoblastogenesis and adipogenesis in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210889/ https://www.ncbi.nlm.nih.gov/pubmed/25310765 http://dx.doi.org/10.3390/md12105132 |
work_keys_str_mv | AT karadenizfatih effectofsalicorniaherbaceaonosteoblastogenesisandadipogenesisinvitro AT kimjungae effectofsalicorniaherbaceaonosteoblastogenesisandadipogenesisinvitro AT ahnbyulnim effectofsalicorniaherbaceaonosteoblastogenesisandadipogenesisinvitro AT kwonmyeongsook effectofsalicorniaherbaceaonosteoblastogenesisandadipogenesisinvitro AT kongchangsuk effectofsalicorniaherbaceaonosteoblastogenesisandadipogenesisinvitro |