首页> 外文期刊>European review for medical and pharmacological sciences. >The bone marrow mononuclear cells reduce the oxidative stress of cerebral infarction through PI3K/AKT/NRF2 signaling pathway
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The bone marrow mononuclear cells reduce the oxidative stress of cerebral infarction through PI3K/AKT/NRF2 signaling pathway

机译:骨髓单个核细胞通过PI3K / AKT / NRF2信号通路降低脑梗死的氧化应激

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OBJECTIVE: To evaluate the mechanism of bone marrow mononuclear cells (BMMNCs) in reducing the oxidative stress after cerebral infarction through PI3K/AKT/NRF2 signaling pathway. MATERIALS AND METHODS: 96 healthy SD rats, which were 6-8-week old, weighting about 250-280 g, were selected for the study. The middle cerebral artery occlusion model (MCAO) was established in SD rats using the suture method. The rats were randomly divided into sham operation group, model group, BMMNCs group and PI3K inhibitor group. 24 rats in each group were selected. 200 μl phosphate-buffered saline (PBS) solution was injected into the caudal vein of the rats in the model group, 200 μl PBS solution containing 5×106 BMMNCs that obtained by gradient centrifugation was injected into the rats in the BMMNCs group, meanwhile, in the PI3K inhibitor group, LY294002 (10 mmol/L/kg) was injected into the lateral ventricle of the brain. After the 3d, 7d and 14d, the modified neurological severity scores (mNSS) were used to evaluate the neurological function. The volume of cerebral infarction was assessed by TTC staining, the VEGF, BDNF, TNF-α, IL-1β, malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) levels were detected by ELISA. RESULTS: The mNSS and the volume of cerebral infarction of the model group were significantly higher than those of the sham operation group (p<0.05), while the mNSS and the volume of cerebral infarction of the BMMNCs group were lower than those of the model group, higher than those of the sham operation group (p<0.05). The VEGF, BDNF, TNF-α, IL-1β, MDA, SOD and GSH-Px levels of the model group were significantly higher than those of the sham operation group (p<0.05). CONCLUSIONS: BMMNCs can reduce the oxidative stress, apoptosis, and inflammatory reaction through PI3K/AKT/NRF2 signaling pathway, thus promoting the secretion of nerve and vascular cytokines, improving the neurological function and reducing the infarct scope.
机译:目的:探讨骨髓单个核细胞(BMMNCs)通过PI3K / AKT / NRF2信号通路降低脑梗死后氧化应激的机制。材料与方法:选择96只6-8周大的健康SD大鼠,体重约250-280 g。采用缝合法在SD大鼠中建立大脑中动脉闭塞模型(MCAO)。将大鼠随机分为假手术组,模型组,BMMNCs组和PI3K抑制剂组。每组选择24只大鼠。将200μl磷酸盐缓冲盐水(PBS)溶液注入模型组的大鼠尾静脉中,将200μl含有5×106 BMMNCs的PBS溶液通过梯度离心法注入BMMNCs组的大鼠中,同时,在PI3K抑制剂组中,将LY294002(10 mmol / L / kg)注入脑侧脑室。 3d,7d和14d后,使用改良的神经系统严重程度评分(mNSS)评估神经功能。通过TTC染色评估脑梗死的体积,通过ELISA检测VEGF,BDNF,TNF-α,IL-1β,丙二醛(MDA),超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)水平。结果:模型组的mNSS和脑梗死体积均显着高于假手术组(p <0.05),而BMMNCs组的mNSS和脑梗死体积均低于模型组。与假手术组比较,差异有统计学意义(p <0.05)。模型组的VEGF,BDNF,TNF-α,IL-1β,MDA,SOD和GSH-Px水平显着高于假手术组(p <0.05)。结论:BMMNCs可以通过PI3K / AKT / NRF2信号通路减少氧化应激,凋亡和炎症反应,从而促进神经和血管细胞因子的分泌,改善神经功能并缩小梗塞范围。

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