黄芪提取物对大鼠全脑缺血再灌注损伤后NFκBp65、ICAM-1和TNF-α表达的影响  

Effects of astragalus extract on NFκBp65,ICAM-1 and TNF-α expression after global cerebral ischemia and reperfusion in rats

作　　者：吴国翠[1] 李静[1] 李卫平[1] 尹艳艳[1] 李维祖[1] 朱芬芳[1] 公惠玲[1] 明亮[1] 吴强[2] 

机构地区：[1]安徽医科大学药理学教研室,合肥230032 [2]安徽医科大学病理学教研室,合肥230032

出　　处：《安徽医科大学学报》2008年第4期406-410,共5页Acta Universitatis Medicinalis Anhui

基　　金：安徽省十五科技重点专项(编号:01803016);安徽省自然科学基金项目(编号:00144414);安徽省教育厅高校省学术带头人后备人选科学研究资助项目(编号:2005HBZ18)

摘　　要：目的探讨黄芪提取物(EA)对大鼠全脑缺血再灌注损伤的保护机制。方法用四动脉阻断法,制备大鼠全脑缺血再灌注模型;采用Western blot检测大鼠全脑缺血再灌注6h后脑皮层组织NFκBp65和IκBα的表达;采用免疫组化(SP法)检测大鼠全脑缺血再灌注24h后脑皮层组织ICAM-1、TNF-α的表达。结果与假手术组相比,模型组大鼠全脑缺血再灌注后脑皮层组织核蛋白NFκBp65(107.1±24.18vs313.09±23.35,P<0.05)表达明显增多,而胞浆蛋白NFκBp65(221.72±19.44vs125.82±25.07,P<0.05)、IκBα(382.98±55.21vs184.37±20.40,P<0.05)表达明显减少;EA可升高大鼠全脑缺血再灌注后脑皮层组织胞浆蛋白NFκBp65、IκBα表达、降低核蛋白NFκBp65表达;同时可降低脑皮层组织ICAM-1、TNF-α的表达。结论EA的脑保护机制可能与抑制大鼠全脑缺血再灌注后NFκBp65活化及降低脑皮质中ICAM-1、TNF-α的表达有关。Objective To explore the mechanisms of neuro-protection effects of astragalus extract （EA） in global cerebral ischemia and reperfusion （I/R） rats. Methods Rats were pretreated ig EA for 5 d and then subjected to global cerebral I/R by four-vessel occlusion method. Expressions of NFκBp65, IκBα in cortex tissue of I/R rats were evaluated with Western blot, and the expressions of ICAM-1 and TNF-α of the cortex tissue were examined by immunohistochemical technical in I/R rats. Results EA increased the expressions of neucleoprotein NFκBp65 （ 107. 1 ±24. 18 vs 313.09 ±23.35,P 〈0. 05） and decreased the expression of plasmosin NFκBp65 （221.72 ± 19. 44 vs 125.82 ± 25.07,P 〈 0. 05 ）, IκBα （382.98 ± 55.21 vs 184. 37 ± 20. 40, P 〈 0. 05 ）. Compared with control group,ICAM-1 and TNF-α expressions during I/R of the group treated with EA were significantly decreased. Conclusion EA has protective effects on cerebral injury through inhibiting the activation of NFκB and decreasing the cortex expressions of ICAM-1 and TNF-α after I/R injury.

关 键 词：黄芪△/药理学 脑缺血 再灌注损伤 肿瘤坏死因子Α 

分 类 号：R282.71[医药卫生—中药学] R322.81[医药卫生—中医学]