Title of article :
Comparison of Osteogenic Potential of Phenytoin with Dexamethasone in Cultured Dental Pulp Stem Cells
Author/Authors :
Tayarani-Najaran, Zahra Medical Toxicology Research Center - Mashhad University of Medical Sciences - Mashhad, Iran , Asgharian-Rezaee, Mitra Department of Toxicology and Pharmacology - Faculty of Pharmacy - Kerman University of Medical Sciences - Kerman, Iran , Alipour-Farmad, Raheleh Department of Toxicology and Pharmacology - Faculty of Pharmacy - Kerman University of Medical Sciences - Kerman, Iran
Abstract :
One of the adverse effects of phenytoin (diphenylhydantoin, DPH) is enlargement of facial
features. Although there are some reports on anabolic action of phenytoin on bone cells, the osteogenic
potential of DPH on mesenchymal stem cells has not been studied. The purpose of this study was to evaluate
the osteogenic potential of DPH on dental pulp stem cells (DPSCs).
Methods: Human DPSCs were isolated and characterized by flow cytometry; presence of CD29 and CD44
and absence of CD34 and CD45 were performed to confirm the mesenchymal stem cells. Isolated DPSCs were
differentiated either in conventional osteogenic medium with Dexamethasone or medium containing different
concentration of phenytoin (12.5, 25, 100, and 200 μM). The osteogenic differentiation evaluated by
performing western blot test for Runt-related transcription factor 2 (RUNX2), osteopontin and alkaline
phosphatase (ALP) also alizarin red S staining to measure the mineralization of cells.
Results: Our results showed morphological changes and mineralization of DPSCs by using DPH were
comparable with dexamethasone. Moreover, western blot results of DPH group showed significant increase of
ALP, RUNX2 and osteopontin (OSP) in comparison with control.
Conclusions: The data of present study showed the osteogenic activity of phenytoin, considering as an
alternative of dexamethasone for inducing osteogenic differentiation of dental pulp stem cells.
Keywords :
Phenytoin , Osteogenic Differentiation , Dental Pulp Stem Cells
Journal title :
Reports of Biochemistry and Molecular Biology (RBMB)