娄海燕, 魏欣冰, 张斌, 孙霞, 张岫美. 羟乙葛根素对大鼠脑缺血再灌注损伤后TNF-α表达及NF-κB活性的影响J. 药学学报, 2007, 42(7): 710-715.
引用本文: 娄海燕, 魏欣冰, 张斌, 孙霞, 张岫美. 羟乙葛根素对大鼠脑缺血再灌注损伤后TNF-α表达及NF-κB活性的影响J. 药学学报, 2007, 42(7): 710-715.
LOU Hai-yan, WEI Xin-bing, ZHANG Bin, SUN Xia, ZHANG Xiu-mei. Hydroxyethylpuerarin attenuates focal cerebral ischemia-reperfusion injury in rats by decreasing TNF-α expression and NF-κB activityJ. Acta Pharmaceutica Sinica, 2007, 42(7): 710-715.
Citation: LOU Hai-yan, WEI Xin-bing, ZHANG Bin, SUN Xia, ZHANG Xiu-mei. Hydroxyethylpuerarin attenuates focal cerebral ischemia-reperfusion injury in rats by decreasing TNF-α expression and NF-κB activityJ. Acta Pharmaceutica Sinica, 2007, 42(7): 710-715.

羟乙葛根素对大鼠脑缺血再灌注损伤后TNF-α表达及NF-κB活性的影响

Hydroxyethylpuerarin attenuates focal cerebral ischemia-reperfusion injury in rats by decreasing TNF-α expression and NF-κB activity

  • 摘要: 观察羟乙葛根素对大鼠局灶性脑缺血再灌注损伤后TNF-α表达及NF-κB活性的影响。采用大鼠大脑中动脉内栓线阻断法(MCAO)建立大鼠脑缺血再灌注损伤模型,分别于缺血前30 min及再灌注即刻由尾静脉注射羟乙葛根素(10,20及40 mg·kg-1),缺血2 h再灌注24 h后取缺血侧脑组织,HE染色观察大鼠脑组织病理学变化并计数海马CA1区存活神经元数目,放射免疫分析测定脑组织匀浆中TNF-α含量,逆转录聚合酶链式反应(RT-PCR)测定脑组织中TNF-α mRNA表达情况,凝胶电泳迁移率实验(EMSA)观察NF-κB DNA结合活性改变,Western blotting检测观察IκBα蛋白表达情况。羟乙葛根素可明显改善大鼠海马CA1区损伤程度,升高锥体存活神经元数目,减少TNF-α蛋白及mRNA表达,抑制NF-κB DNA结合活性。羟乙葛根素可减轻大鼠脑缺血再灌注损伤后炎症反应,这可能是其发挥脑保护作用的机制之一。

     

    Abstract: This study is to investigate the effect of hydroxyethylpuerarin on the expression of tumor necrosis factor-alpha (TNF-α) and activity of nuclear factor kappa B (NF-κB) after middle cerebral artery occlusion (MCAO) in rats. Rats were subjected to cerebral ischemia-reperfusion injury induced by MCAO. Hydroxyethylpuerarin (10, 20, 40 mg·kg-1, iv) was administered just 30 min before occlusion and immediately after reperfusion. After a 24 h reperfusion following 2 h of MCAO, the number of viable neurons in hippocampal CA1 region was counted by hematoxylin and eosin (HE) staining. TNF-α protein and its mRNA expression were examined with radioimmunoassay (RIA) and reverse transcriptase-polymerase chain reaction (RT-PCR) respectively. NF-κB activity was observed by electrophoretic mobility shift assay (EMSA), and inhibition of NF-κB α (IκBα) protein expression was evaluated by Western blotting analysis. Animals treated with hydroxyethylpuerarin had a significant increase in neuronal survival in comparison with vehicle-treated group. Hydroxyethylpuerarin significantly reduced the protein and mRNA expression of TNF-α following 2 h of ischemia with 24 h of reperfusion. NF-κB DNA binding activity and the degradation of IκBα in the cytoplasm also decreased by hydroxyethylpuerarin treatment. The protective effects of hydroxyethylpuerarin against ischemia-reperfusion injury may be mediated by decreasing the expression of TNF-α and the activity of NF-κB in rats.

     

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