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Accelerators of Osteogenesis by Recombinant Human Bone Morphogenetic Protein-2

Bone morphogenetic protein (BMP) appears to be one of the most promising cytokine and for clinical use in reconstructive surgery for bony defects and augmentation. To evaluate the effect of basic fibroblast growth factor (bFGF), FK506, elcatonin, and hyperbaric oxygenation (HBO) on osteoinduction by...

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Autores principales: Okubo, Yasunori, Kusumoto, Kenji, Bessho, Kazuhisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3155240/
https://www.ncbi.nlm.nih.gov/pubmed/21901062
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author Okubo, Yasunori
Kusumoto, Kenji
Bessho, Kazuhisa
author_facet Okubo, Yasunori
Kusumoto, Kenji
Bessho, Kazuhisa
author_sort Okubo, Yasunori
collection PubMed
description Bone morphogenetic protein (BMP) appears to be one of the most promising cytokine and for clinical use in reconstructive surgery for bony defects and augmentation. To evaluate the effect of basic fibroblast growth factor (bFGF), FK506, elcatonin, and hyperbaric oxygenation (HBO) on osteoinduction by recombinant human bone morphogenetic protein-2 (rhBMP-2), 2 or 5 μg of rhBMP-2 was implanted into intramuscular sites of rats. At 21 days after implantation, the osteoinductive activity in the treatment group and control group was compared radiographically, biochemically, and histologically. The amount of new bone in the treatment group was significantly greater than that in the control group. The alkaline phosphatase activity and calcium content in the treatment group were significantly higher than those in the control group. These results suggest that bFGF, FK506, elcatonin, and HBO accelerated the activity and rate of osteoinduction by rhBMP2. These results may be useful when BMP is applied clinically in near future.
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spelling pubmed-31552402011-09-07 Accelerators of Osteogenesis by Recombinant Human Bone Morphogenetic Protein-2 Okubo, Yasunori Kusumoto, Kenji Bessho, Kazuhisa Drug Target Insights Rapid Communication Bone morphogenetic protein (BMP) appears to be one of the most promising cytokine and for clinical use in reconstructive surgery for bony defects and augmentation. To evaluate the effect of basic fibroblast growth factor (bFGF), FK506, elcatonin, and hyperbaric oxygenation (HBO) on osteoinduction by recombinant human bone morphogenetic protein-2 (rhBMP-2), 2 or 5 μg of rhBMP-2 was implanted into intramuscular sites of rats. At 21 days after implantation, the osteoinductive activity in the treatment group and control group was compared radiographically, biochemically, and histologically. The amount of new bone in the treatment group was significantly greater than that in the control group. The alkaline phosphatase activity and calcium content in the treatment group were significantly higher than those in the control group. These results suggest that bFGF, FK506, elcatonin, and HBO accelerated the activity and rate of osteoinduction by rhBMP2. These results may be useful when BMP is applied clinically in near future. Libertas Academica 2007-02-21 /pmc/articles/PMC3155240/ /pubmed/21901062 Text en © the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited.
spellingShingle Rapid Communication
Okubo, Yasunori
Kusumoto, Kenji
Bessho, Kazuhisa
Accelerators of Osteogenesis by Recombinant Human Bone Morphogenetic Protein-2
title Accelerators of Osteogenesis by Recombinant Human Bone Morphogenetic Protein-2
title_full Accelerators of Osteogenesis by Recombinant Human Bone Morphogenetic Protein-2
title_fullStr Accelerators of Osteogenesis by Recombinant Human Bone Morphogenetic Protein-2
title_full_unstemmed Accelerators of Osteogenesis by Recombinant Human Bone Morphogenetic Protein-2
title_short Accelerators of Osteogenesis by Recombinant Human Bone Morphogenetic Protein-2
title_sort accelerators of osteogenesis by recombinant human bone morphogenetic protein-2
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3155240/
https://www.ncbi.nlm.nih.gov/pubmed/21901062
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