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Background and Objective: Research have been focused on the applying the chemical inducer for trans-differentiation the adult BMSCs into neural cell. So that, at the first should investigate the toxcity effect of the chemical inducer on the induced cells. Plasticity and easy accessibility of bone marrow mesenchymal stem cells is a unique charactristic for treatment of neural disorderies. This study was desgined to determine the inductive effect of Deprenyl and Dimethyl sulfoxide on proliferation and survival of the mesenchymal stem cells. Materials and Methods: In this experimental study, BMSCs isolated from the adult rat bone marrow and cultured in αMEM containing 10% FBS. Cell identity for surface antigens was performed in third passage by immunocytochemistry and multipotancy capacity of BMSCs was done by BMSC differentiation into adipocytes and osteocytes. The cells were exposed to chemical agents (a: the αMEM medium supplemented with 2% DMSO, b: the αMEM medium supplemented with 10^-8M Deprenyl) for 24 houres and then transferred to αMEM containing 10% FBS cell survival and proliferation was evaluated after the 24, 48, 72 and 96 houres by MTT [3-(4-5-Dimethylthiazolyl-2-y1)-2,5-diphenyltetrazolium bromid] test. Data were analyzed using SPSS-16, One-Way ANOVA and Tukey tests. Results: In addition to expression the surface antigens and adipogenic and osteogenic differentiation by BMSCs, MTT test results showed that proliferation and survival of induced-deprenyl and DMSO cells within 48, 72 and 96 hours after the induction was increased significantly than negative control group. Conclusion: Deprenyl increases survival and cell proliferation compared to Dimethyl Sulfoxide. It can be used as cell inducer.

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Background and Objective: Stem cells are a suitable treatment method for improvement of central nervous system diseases. Neuron regeneration is occure in damaged region using stem cell transplantation. This study was done to determine the effect of bone marrow mesenchymal stem cells on memory and neuronal cells graft number in the trimethyltin chloride damaged hippocampus. Methods: In this experimental study, 28 wistar male rats were allocated into four groups including control, model, Vehicle and treatment groups. Animals were received 8 mg/kg/bw of neurotoxin trimethyltin chloride by the intraperitoneal injection for causing damaged in hippocampus. One week after intraperitoneal injection of trimethyltin chloride, stem cells was injected by stereotaxy method. Six weeks after stem cells injection, the spatial memory was assessed by Morris water maze and histological studies were done by Nissl staining and normal cells count by Olysia bio report software. Results: After bone marrow mesenchymal stem cells graft, the number of normal cells were more in the treatment group (74±15.190) in compared to the Vehicle (44.67±12.971) and Model (48.56±18.105) groups (P<0.05). Also in Morris water maze test, the treatment group (387.35±189.18), (31.30±13.67) spent shorter distance and escape latency to reach the hidden platform, but this reduced non significantly in compared to Vehicle (438.18±192.56), (40.14±14.89) and model (407.98±225.44), (37.68±17.15) groups. The model and Vehicle groups spent longer distance to reach the hidden platform in comparision with the control (275.45±165.10) group (P<0.05). Also the traveled distance in target quarter had significant increased in the treatment groups (799.80±125.91) in compared to model (588.51±136.94) and Vehicle (546.48±86.47) groups (P<0.05). Conclusion: Using the bone marrow mesenchymal stem cells leads to reduce hippocampal lesions and increase the number of pyramidal neurons and improving memory in damaged hippocampus in animal model.

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Background and Objective: Cardiovascular diseases and heart failure are major diseases in developed countries. Stem cells showed specific features to play an important role in heart disease treatment. One of the most common compounds has been used to induce differentiation of stem cells into cardiomyocyte is 5-Azacytidine. Medium contents of cell culture such as different glucose concentrations also influence on morphology and function of final differentiated cells. This study was done to evaluate the effect of glucose on improvement of BM-MSC differentiation into cardiomyocyte - like cells.
Methods: In this experimental study, effect of two different glucose concentrations (5 and 25mM) on the mesenchymal stem cells differentiation (MSCs) to cardiomyocytes during 21 days was evaluated. Bone marrow MSCs (BM MSCs) seeded in differentiation medium which treated with 5-aza and 5 & 25mM glucose concentrations. In next step, total RNA was extracted and cDNA synthesis was carried out. Finally, quantitative polymerase chain reaction (Q-PCR) was done to determine level of cardiac-specific markers during differentiation process including Connexin43, α-cardiac actin, TroponinT and TroponinI.
Results: Level of cardiac-specific markers during differentiation of mesenchymal stem cells to cardiomyocyte including Connexin43, α-cardiac actin, TroponinT and TroponinI in 5 and 25 mM of glucose concentration was diferent, but this diference was not significant.
Conclusion: Our results showed that two concentrations of glucose (5, 25mM) have no remarkable effect on the expression of cardiac markers during differentiation of bone marrow mesenchymal stem cells to cardiomyocyte.