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骨髓单核细胞通过 PI3K/AKT/NRF2 信号通路减轻脑梗死的氧化应激。

The bone marrow mononuclear cells reduce the oxidative stress of cerebral infarction through PI3K/AKT/NRF2 signaling pathway.

机构信息

Department of Neurology, The fifth Affiliated Hospital of Zhengzhou University, Zhengzhou City, Henan Province, P.R. China.

出版信息

Eur Rev Med Pharmacol Sci. 2017 Dec;21(24):5729-5735. doi: 10.26355/eurrev_201712_14019.

Abstract

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.

摘要

目的

通过 PI3K/AKT/NRF2 信号通路评估骨髓单核细胞(BMMNCs)减少脑梗死后氧化应激的机制。

材料和方法

选择 96 只 6-8 周龄、体重约 250-280g 的健康 SD 大鼠进行研究。采用缝线法建立 SD 大鼠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 24 只大鼠。模型组大鼠尾静脉注射 200μl 磷酸盐缓冲液(PBS)溶液,BMMNCs 组大鼠尾静脉注射经梯度离心获得的 200μl PBS 溶液,同时,PI3K 抑制剂组大鼠脑室内注射 LY294002(10mmol/L/kg)。3d、7d、14d 后,采用改良神经功能缺损评分(mNSS)评估神经功能,TTC 染色评估脑梗死体积,ELISA 法检测 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 mNSS 和脑梗死体积明显高于假手术组(p<0.05),BMMNCs 组 mNSS 和脑梗死体积低于模型组,高于假手术组(p<0.05)。模型组 VEGF、BDNF、TNF-α、IL-1β、MDA、SOD 和 GSH-Px 水平明显高于假手术组(p<0.05)。

结论

BMMNCs 可通过 PI3K/AKT/NRF2 信号通路减轻氧化应激、细胞凋亡和炎症反应,促进神经和血管细胞因子的分泌,改善神经功能,减少梗死范围。

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