TY - JOUR ID - 13098 TI - The mechanism of neuroprotective effect of Viola odorata against serum/glucose deprivation-induced PC12 cell death JO - Avicenna Journal of Phytomedicine JA - AJP LA - en SN - 2228-7930 AU - Tayarani Najjaran, Zahra AU - Yazdian, Rezvan AU - Amini, Elaheh AU - Salek_Abdollahi, Farzaneh AU - Arasteh, Fatemeh AU - Emami, Ahmad AD - Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran. AD - Molecular and Cell Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran. AD - Department of Cellular and Molecular Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran. AD - Department of Biology, Faculty of Sciences, Mashhad Branch, Islamic Azad University, Mashhad, Iran. AD - Department of Pharmaceutical Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran AD - Department of Traditional Pharmacy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran. Y1 - 2019 PY - 2019 VL - 9 IS - 6 SP - 491 EP - 498 KW - Viola odorata KW - Violaceae KW - PC12 cells KW - ROS KW - SGD DO - 10.22038/ajp.2019.13098 N2 - Objective: Oxidative stress is associated with the pathogenesis of brain ischemia and other neurodegenerative disorders. Previous researches have shown the antioxidant activity of Viola odorata L. In this project, we studied neuro-protective and reactive oxygen species (ROS) scavenging activities of methanol  (MeOH) extract and other fractions isolated from V. odorata in PC12 cell line in serum/glucose deprivation  (SGD) condition. Materials and Methods: The PC12 neuronal cells were pretreated for 6 hr with MeOH extract and fractions of V. odorata (1 to 25 μg/ml) followed by 24 hr incubation under SGD condition. Cell viability was measured by Alamar Blue® assay. The level of ROS was calculated using DCFH-DA. Also, Bax/Bcl-2 protein ratio was analyzed by western blot assay. Results: SGD condition significantly decreased cells viability (p<0.001). Pretreatment with EtOAc (12.5 and 25 µg/ml), BuOH (12, 25, 50 µg/ml) and CH2Cl2 (1.5 µg/ml) fractions of V. odorata reduced SGD-induced cytotoxicity. MeOH extract could not increase the viability significantly. All four semi polar fractions (EtOAc, BuOH, CH2Cl2 and MeOH) decreased SGD-induced ROS production and changed Bax/Bcl-2 ratio. Conclusion: V. odorata showed promising effects against SGD condition; further mechanistic and clinical studies are warranted before application of V. odorata as a neuro-protective agent. UR - https://ajp.mums.ac.ir/article_13098.html L1 - https://ajp.mums.ac.ir/article_13098_346b239ac3095c7c0c1a1b1ff586095f.pdf ER -