张国红, 吕平, 王永利. 双苯氟嗪对大鼠局灶性脑缺血再灌注后E-选择素、P-选择素和细胞间黏附分子-1表达的影响J. 药学学报, 2005, 40(12): 1091-1095.
引用本文: 张国红, 吕平, 王永利. 双苯氟嗪对大鼠局灶性脑缺血再灌注后E-选择素、P-选择素和细胞间黏附分子-1表达的影响J. 药学学报, 2005, 40(12): 1091-1095.
ZHANG Guo-hong, Lü Ping, WANG Yong-li. Effects of dipfluzine on expressions of E-selectin, P-selectin, and ICAM-1 in brain ischemia-reperfusion ratsJ. Acta Pharmaceutica Sinica, 2005, 40(12): 1091-1095.
Citation: ZHANG Guo-hong, Lü Ping, WANG Yong-li. Effects of dipfluzine on expressions of E-selectin, P-selectin, and ICAM-1 in brain ischemia-reperfusion ratsJ. Acta Pharmaceutica Sinica, 2005, 40(12): 1091-1095.

双苯氟嗪对大鼠局灶性脑缺血再灌注后E-选择素、P-选择素和细胞间黏附分子-1表达的影响

Effects of dipfluzine on expressions of E-selectin, P-selectin, and ICAM-1 in brain ischemia-reperfusion rats

  • 摘要: 目的研究双苯氟嗪对大鼠脑缺血再灌注后E-选择素(E-selectin)、P-选择素(P-selectin)和细胞间黏附分子-1(ICAM-1)表达及中性粒细胞浸润的影响。方法采用Zea-Longa线栓法建立大鼠局灶性脑缺血再灌注模型。采用HE染色、免疫组化、流式细胞术以及生化的方法,观察双苯氟嗪对大鼠缺血再灌注后脑组织形态学、P-选择素、E-选择素和ICAM-1表达以及髓过氧化酶(MPO)活性的影响。结果双苯氟嗪可改善缺血再灌注后脑损伤的形态学表现;降低P-选择素、E-选择素和ICAM-1的表达以及MPO的活性。结论双苯氟嗪减轻缺血再灌注后炎症反应,对缺血再灌注性脑损伤具有保护作用。

     

    Abstract: AimTo evaluate the effects of dipfluzine on the expressions of E-selectin, P-selectin, and ICAM-1 and the infiltration of polymorphonuclear leukocytes in brain ischemia-reperfusion rats. MethodsThe model of focal cerebral ischemia was established with the Zea-Longa occluding suture. Dipfluzine (0.25, 0.5 and 1 mg·kg-1), flunarizine 0.5 mg·kg-1 and solvent were injected separately into lingual vein at 30 min after ischemia. The occluding suture was slowly taken away to cause reperfusion at 1 h after ischemia. Rats were decapitated under anesthesia at 24 h after ischemia-reperfusion and brains were immediately removed to do the following procedures. Effects of dipfluzine on morphology of the brain tissue were observed through hematoxylin-eosin (HE) staining. By immunohistochemistry and flow cytometry technique and biochemical method, effects of dipfluzine on P-selectin, E-selectin, ICAM-1 and myeloperoxidase (MPO) were observed. ResultsDipfluzine could relieve pathological damages in the brain tissue after ischemia-reperfusion, and reduce the expressions of E-selectin, P-selectin and ICAM-1 and activities of MPO in dose-dependent manner. ConclusionDipfluzine depresses the expressions of P-selectin, E-selectin,and ICAM-1, which are correlated with their effects on the activities of MPO, suggesting that dipfluzine has anti-inflammation effect in certain extent and could protect brain tissue from ischemia-reperfusion injury.

     

/

返回文章
返回