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作 者:尹艳艳[1] 李卫平[1] 王绍斌[1] 何婷[1] 明亮[1]
机构地区:[1]安徽医科大学药理学教研室,安徽合肥230032
出 处:《中国药理学通报》2005年第12期1486-1489,共4页Chinese Pharmacological Bulletin
基 金:安徽省"十五"科技重点专项课题资助项目(No01803016);安徽省自然科学基金资助项目(No00144414)
摘 要:目的研究黄芪提取物(EA)对局灶性脑缺血再灌注损伤的保护作用机制。方法采用线栓法大鼠局灶性脑缺血再灌注损伤模型,以免疫组化法观察EA对缺血再灌注后大鼠脑组织中TNFα表达的影响、以放免法观察对IL1β水平的影响、以TUNEL法观察对脑组织细胞凋亡的影响。结果与模型组比较,EA(20、40、80mg·kg-1,ig)能减少TNFα的表达、降低IL1β水平和减少细胞凋亡数。结论EA对大鼠局灶性脑缺血再灌注后脑组织中TNFα及IL1β的升高和神经元的凋亡有明显的抑制作用。Aim To study the mechanisms of protective effects of extract of astragalus against focal cerebral ischemia/reperfusion injury in rats. Methods Focal cerebral ischemia was induced by intraluminal thread occlusion of middle cerebral artery. Immunohistochemistry was used to determine expression of TNF-α, IL-1β was measured by radioimmunity, and the apoptosis was observed by TUNEL. Results EA (20,40,80 mg ·kg^-1, ig ) could decrease the expression of TNF-α and the level of IL-1β and reduce cell apoptosis. Conclusion EA has inhibitory action on the increase in the expression of TNF-α, the level of IL-1β and the apoptosis of neurons induced by focal cerebral ischemia/ reperfusion.
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