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Background and Objective: Lead threaten living creature’s life as air pollutant and causes several diseases such as degenerative disease of nervous system. This research was conducted to determine the effect of Curcumin on BDNF changes and oxidative/antioxidative process in rat’s hippocampus which exposed to Lead acetate.

Materials and Methods: In this experimental study, 40 male Wistar rats were randomly assigned to four groups of ten: Base, Sham(control), lead and Curcumin+Lead. lead and Curcumin+Lead groups received 20 mg/kg lead acetate and Curcumin+Lead group also received 30 mg/kg Curcumin, peritoneally for 8 weeks (3 days in weeks). MDA (oxidative stress biomarker) and TAC (total antioxidative capacity) levels were measured by TBARS and FRAP methods, respectively, and hippocampus BDNF level was measured by ELISA method in rat hippocampus region. Data was analyzed by one-way ANOVA test and Tukey at P<0.05 level.

Results: Injection of lead acetate significantly increased MDA, non-significantly decreased hippocampus BDNF and significantly decreased TAC levels in the Lead group compared with control groups. On the other hand, curcumin administration led to non significantly decreased MDA, nonsignificantly increased BDNF and significantly increased TAC levels compared with other groups (P<0.05).

Conclusion: This study showed that Curcumin adminstration in long term lead acetate-treated male Wistar Rats did not increased BDNF of hippocampus, but it prevent the reduction of BNDF due to lead-intoxification.

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Background and Objective: Neurotrophic factors are diffusible polypeptides that have critical roles in survival, proliferation and differentiation of stem cells. This study was done to assess the role of neurotrophic factors (CNTF‎, BDNF, ‎GDN‎F, ‎NT-‎3‎) expression and proliferation rate of neural stem cells (NSCs) in coculture with mesenchymal stem cells (MSCs). Materials and Methods: In this experimental study, NSCs and MSCs were isolated from adult Wistar rat. Initially, NSCs was harvested from temporal lobe after mechanical digestion by a sterile flamed Pasteur pipette and enzymatic digestion with trypsin and Dnase. The cell suspension was cultivated in a flask with DMEM/F12 medium supplemented with 10% FBS 100U/ml Penicillin and 100 mg/ml Streptomycin. To obtain MSCs, bone marrow of femur and tibia bones were flashed out and cultured. MSCs and NSCs‎ cocultured by transwell ‎system in DMEM/F12 medium supplemented with 10% FBS 100U/ml Penicillin and 100 mg/ml Streptomycin. Haemocytometer, immunocytochemistry and RT-PCR methods were performed to identify and evaluate cell proliferation, purity levels and neurotrophic factors expression. Results: There ‎is‎ no differences in NTFs profile of ‎neurotrophic‎ factors expression between ‎coculture ‎group‎ ‎and‎ control ‎NSCs, but interactions between MSCs and NSCs significantly promoted NSCs proliferation (P<0.05). Conclusion: This study showed that coculture of NSCs with MSCs might be prfered in cell-therapy than‎ NSCs.‎