Volume 25, Issue 112 (7-2017)                   J Adv Med Biomed Res 2017, 25(112): 72-85 | Back to browse issues page

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Gholinejad M, Abdanipour A R, Taromchi A H, Jafari Anar Kooli I, Nikfar A. Evaluation of Neuroprotective Effect of Adenosine on Neural Stem Cells exposed to Oxidative Stress Condition with H2O2. J Adv Med Biomed Res 2017; 25 (112) :72-85
URL: http://journal.zums.ac.ir/article-1-4606-en.html
1- Dept. of Medical Biotechnology and Nanotechnology, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran
2- Dept. of Anatomy, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran
3- Dept. of Genetics and Molecular Medicine, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran
Abstract:   (150134 Views)

Background and Objective: Excessive production of free radicals during oxidative stress can cause serious damage to important biomolecules and activate programmed cell death pathways in the body. In the nervous system, neuronal cell death leads to many progressive neurodegenerative disorders. The aim of this study was to evaluate the effects of adenosine on the inhibition of apoptosis in oxidative damage induced by hydrogen peroxide in bone marrow derived neural stem cells (BMSCs-dNSCs).

Materials and Methods: BMSCs-dNSCs were pretreated with different doses of adenosine for 48 hours and then exposed to 125μM H2O2 for 30 minutes. Using MTT and TUNEL assay, we evaluated the effects of adenosine on cell survival and apoptosis in pretreated BMSCs-dNSCs in comparison to control groups.

Results: The results showed that the apoptosis rate in the 6 µM adenosine pretreated BMSCs-dNSCs was significantly decreased compared to the control group in the condition of oxidative stress (P<0.05).  

Conclusion: Our findings suggest that adenosine protects NSCs against oxidative stress induced cell death, therefore it may be used to promote the survival rate of NSCs and could be a candidate for the treatment of oxidative stress mediated neurological diseases.

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Type of Study: Clinical Trials |
Received: 2017/06/17 | Accepted: 2017/06/17 | Published: 2017/06/17

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