Author/Authors :
Attari, Fatemeh Department of Neuroscience - School of Advanced Technologies in medicine - Tehran University of Medical Sciences - Shefa Neuroscience Research Center - Khatamolanbia Hospital, Tehran , Zahmatkesh, Maryam Department of Neuroscience - School of Advanced Technologies in medicine - Tehran University of Medical Sciences , Aligholi, Hadi Department of Neuroscience - School of Advanced Technologies in medicine - Tehran University of Medical Sciences - Shefa Neuroscience Research Center - Khatamolanbia Hospital, Tehran , Ejtemaei Mehr, Shahram Department of Pharmacology - School of Medicine -Tehran University of Medical Sciences, Tehran , Sharifzadeh, Mohammad Faculty of Pharmacy and Pharmaceutical Sciences Research Center - Tehran University of Medical Sciences, Tehran , Gorji, Ali Epilepsy Research Center - WestfälischeWilhelms-UniversitätMünster - Münster, Germany , Mokhtari, Tahmineh Department of Anatomy - School of Medicine - Tehran University of Medical Sciences, Tehran , Khaksarian, Mojtaba Department of Physiology - Medical College - Lorestan University of Medical Sciences, Khorramabad , Hassanzadeh, Gholamreza Department of Neuroscience - School of Advanced Technologies in medicine - Tehran University of Medical Sciences - Department of Anatomy - School of Medicine - Tehran University of Medical Sciences, Tehran
Abstract :
Background: The beneficial effects of curcumin which includes its antioxidant, anti-inflammatory and cancer chemo-preventive properties have been identified. Little information is available regarding the optimal dose and
treatment periods of curcumin on the proliferation rate of different sources of stem cells.
Methods: In this study, the effect of various concentrations of curcumin on the survival and proliferation of two types
of outstanding stem cells which includes bone marrow stem cells (BMSCs) and adult rat neural stem/progenitor cells
(NS/PCs) at different time points was investigated. BMSCs were isolated from bilateral femora and tibias of adult Wistar
rats. NS/PCs were obtained from subventricular zone of adult Wistar rat brain. The curcumin (0.1, 0.5, 1, 5 and 10 μM/L)
was added into a culture medium for 48 or 72 h. Fluorescent density of 5-bromo-2′-deoxyuridine (Brdu)-positive cells
was considered as proliferation index. In addition, cell viability was assessed by MTT assay.
Results: Treatment of BMSCs with curcumin after 48 h, increased cell survival and proliferation in a dose-dependent
manner. However, it had no effect on NSCs proliferation except a toxic effect in the concentration of 10 μM of curcumin.
After a 72 h treatment period, BMSCs and NS/PCs survived and proliferated with low doses of curcumin. However, high
doses of curcumin administered for 72 h showed toxic effects on both stem cells.
Conclusions: These findings suggest that curcumin survival and proliferative effects depend on its concentration,
treatment period and the type of stem cells. Appropriate application of these results may be helpful in the outcome of
combination therapy of stem cells and curcumin.
Keywords :
Curcumin , Bone marrow mesenchymal stem cells , Neural stem cells , Cell proliferation , Cell survival