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Gastrodia and Uncaria (tianma gouteng) water extract exerts antioxidative and antiapoptotic effects against cerebral ischemia in vitro and in vivo

机译:天麻和钩藤提取物在体外和体内对脑缺血具有抗氧化和抗凋亡作用

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Background Gastrodia and Uncaria decoction (tianma gouteng yin) is commonly used in Chinese medicine to treat cerebral ischemia. The aim of this study was to investigate the neuroprotective effects of a water extract (GUW) of Gastrodia elata (tianma; GE) and Uncaria rhynchophylla (gouteng; UR) against ischemic insult using oxygen-glucose-deprived neuronal differentiated PC12 cells and rats subjected to middle cerebral artery occlusion (MCAO). Methods GUW was prepared by boiling raw GE and UR in water, followed by the lyophilization of the resulting extract. Neuronal differentiated PC12 cells were subjected to oxygen-glucose deprivation with or without GUW. The neuroprotective effects of GUW were compared with those of the corresponding GE and UR extracts to tease apart the effects of the different herbs. The synergistic effect of GE and UR in GUW was measured using a modified version of Burgi’s formulae. The neuroprotective mechanisms via Nrf2 and anti-apoptotic pathways were investigated using real time PCR and enzyme activity assays. The neuroprotective effects of GUW were studied in vivo using a rat MCAO model. Neurofunctional outcome and brain infarct volume we assessed. H&E staining, cresyl violet staining and immunohistochemistry were performed to assess the histological outcome. Results The results of lactate dehydrogenase assay showed that GUW protected cells in a concentration-dependent manner ( P Conclusion GUW modulated the antioxidant system and antiapoptotic genes in oxygen-glucose deprived neuronal differentiated PC12 cells and MCAO sprague–dawley rats.
机译:背景天麻和钩藤汤(天麻钩藤饮)常用于中药治疗脑缺血。这项研究的目的是研究天麻,天麻和钩藤Uncaria rhynchophylla(gouteng; UR)的水提取物(GUW)对缺氧-葡萄糖剥夺的神经元分化的PC12细胞和大鼠的缺血损伤的神经保护作用。到大脑中动脉闭塞(MCAO)。方法GUW的制备方法是将GE和UR原料在水中煮沸,然后将所得提取物冻干。在有或没有GUW的情况下,对神经元分化的PC12细胞进行氧葡萄糖剥夺。将GUW的神经保护作用与相应的GE和UR提取物的神经保护作用进行了比较,以阐明不同草药的作用。 GE和UR在GUW中的协同作用是使用Burgi公式的改进版本进行测量的。使用实时PCR和酶活性测定法研究了通过Nrf2和抗凋亡途径的神经保护机制。使用大鼠MCAO模型在体内研究了GUW的神经保护作用。我们评估了神经功能结局和脑梗死体积。进行H&E染色,甲酚紫染色和免疫组织化学以评估组织学结果。结果乳酸脱氢酶测定结果表明,GUW以浓度依赖的方式保护细胞(P结论GUW调节了缺氧-葡萄糖剥夺的神经元分化的PC12细胞和MCAO鼠-道来大鼠的抗氧化系统和抗凋亡基因。

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