首页> 外文期刊>Jundishapur Journal of Natural Pharmaceutical Products >Synergistic and Defensive Properties of Emblica officinalis, Terminalia chebula, and Terminalia bellerica Extracts Against Serum/Glucose Deprivation-Induced PC12 Cells Death
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Synergistic and Defensive Properties of Emblica officinalis, Terminalia chebula, and Terminalia bellerica Extracts Against Serum/Glucose Deprivation-Induced PC12 Cells Death

机译:余甘子,榄仁,榄仁提取物对血清/葡萄糖剥夺诱导的PC12细胞死亡的协同和防御特性。

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Background: Triphala as a combination of three planta??s fruits including Emblica officinalis Gaertn, Terminalia chebula Retz, and Terminalia bellerica Roxb is valued for its antioxidant properties. It has been routinely used in various medicinal studies. Objective: In this study, the protective effects of E. officinalis, T. chebula, T. bellerica, and Triphala methanolic extracts on cell viability and reactive oxygen species (ROS) generated in PC12 cells were studied under serum/glucose deprivation (SGD) induced cell injury. Synergistic activity of three extracts was also explored. Methods: Cells were seeded overnight and then exposed to SGD condition for 18 h. Next, they were pretreated with different concentrations of the four extracts (3 - 250 ?μg/ml) for 4 h. Cell viability and ROS generation were evaluated by viability assay and flow cytometry, respectively. Synergistic activity of three extracts was analyzed with Compusyn software. Results: SGD could induce cell toxicity after 18 h (P 0.001). Pretreatment with extracts reduced SGD toxicity in PC12 cells. A signi???cant raise in ROS generation was seen following SGD-induced toxicity. Pretreatment with T. chebula reversed the increased ROS production following ischemic insult. Conclusions: These results demonstrated the neuroprotection of these extracts possibly by ROS decrement and synergistic activity of them against SGD-induced toxicity.
机译:背景:Triphala是三种植物的果实的组合,包括Embica officinalis Gaertn,Terminalia chebula Retz和Bellerica bellerica Roxb,其抗氧化性能得到重视。它已被常规用于各种医学研究中。目的:在血清/葡萄糖剥夺(SGD)下,研究了厚朴,厚朴,甜菜和Triphala甲醇提取物对PC12细胞活力和活性氧(ROS)的保护作用。诱导细胞损伤。还探讨了三种提取物的协同活性。方法:将细胞接种过夜,然后暴露于SGD条件下18 h。接下来,将它们用不同浓度的四种提取物(3-250微克/毫升)预处理4小时。通过活力测定和流式细胞术分别评估细胞活力和ROS产生。用Compusyn软件分析三种提取物的协同活性。结果:SGD可在18 h后诱导细胞毒性(P <0.001)。提取物预处理可降低PC12细胞中SGD的毒性。在SGD诱导的毒性之后,观察到ROS产生的显着增加。用T. chebula预处理可逆转缺血性损伤后ROS产生的增加。结论:这些结果证明了这些提取物的神经保护作用可能是由于ROS下降以及它们对SGD诱导的毒性的协同活性所致。

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