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醒脑开窍针法对脑缺血再灌注后细胞间黏附分子-1和P-选择素表达调节的实验研究 被引量:3

Effect of Xingnao Kaiqiao Acupuncture on Expression of ICAM-1 and P-selectin after Cerebral Ischemia and Reperfusion in Rat
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摘要 [目的]探讨醒脑开窍针刺法治疗抗脑缺血再灌注炎性损伤的机制。[方法]采用大脑中动脉线栓法制备大脑中动脉栓塞(MCAO)缺血再灌注模型,运用原位杂交和免疫组织化学技术动态观察脑缺血1h,再灌注3、6、12、24、48h大鼠大脑缺血侧皮层、纹状体细胞间黏附分子-1(ICAM-1)、P-选择素(P-selectin)mRNA、蛋白表达和电针的调节作用。[结果]脑缺血区的毛细血管内皮细胞表达ICAM-1和P-selectinmRNA发生于脑缺血/再灌注后3h,ICAM-1mRNA在脑缺血/再灌注12h达到高峰(组内比较,P<0.01);P-selectinmRNA高峰出现在脑缺血/再灌注6~12h(组内比较,P<0.01)。脑缺血区毛细血管ICAM-1和P-selectin蛋白表达发生于脑缺血/再灌注后3h,高峰均出现于脑缺血再灌注24h(模型组与假手术组比较P<0.01),并持续至脑缺血再灌注后48h;醒脑开窍针刺法可显著降低缺血区ICAM-1和P-selectinmRNA和蛋白表达(治疗组与模型组比较P<0.01)。[结论]早期醒脑开窍针刺法治疗可能通过下调脑缺血区黏附分子ICAM-1和P-selectin的mRNA和蛋白表达而防治脑缺血再灌注炎性损伤。 [Objective] To explore the mechanism of Xiangnao kaiqiao(represhment and Inducing resuscitation) acupuncture against cerebral ischemia and reperfusion injury. [Methods] The cerebral ischemia and reperfusion injury was established by lineembolism of cerebral middle artery. The expression of ICAM-1 and P-selectin mRNA and protein in ischemic cerebral cortex and corpus striatum in rat was observed after 1 h of cerebral ischemia and 3,6,12,24 and 48 h of reperfusion by in situ hybridizatioin and immunohistochemistry. [Results] The mRNA expression of ICAM-1 and P-selectin was found at the capillary endothelial cells in the postischemia cerebral cortex 3 h after reperfusion and peaked at 12 h and 6-12 h respectively(P〈0.01) and increased continually during 48 reperfusion. Both expressions of mRNA and protein of ICAM and P-selectin in ischemia cerebral cortex were down-regulated considerably by Xiangnao Kaiqiao acupuncture(P〈0.01). [Conclusion] The Xingnao Kaiqiao acupuncture method may prevent and cure the cerebral ischemia and reperfusion injury by down-regulating the expression of mRNA and protein of ICAM -1 and P-selectin in ischemia cerebral cortex.
出处 《天津中医药》 CAS 2005年第6期462-466,共5页 Tianjin Journal of Traditional Chinese Medicine
关键词 醒脑开窍针法 脑缺血再灌注 细胞问黏附分子-1 P-选择素 Xingnao Kaiqiao acupuncture cerebral ischemia and reperfusion ICAM-1 P-selectin
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