目的:探讨麝香、冰片对脑缺血-再灌注损伤大鼠急性期及恢复早期的保护作用及机制。方法:将180只大鼠随机分为假手术组,模型组,麝香高、低剂量组(50、25 mg/kg),冰片高、低剂量组(50、25 mg/kg),醒脑静10m L/kg组。各组大鼠灌胃给药4 d,线栓法复制脑缺血-再灌注模型,观察麝香、冰片对脑缺血-再灌注炎性损伤急性期及恢复早期神经功能缺损评分、脑组织匀浆环氧酶(COX-2)和5脂氧酶(5-LOX)活性变化及海马组织Cys LT2蛋白及mRNA表达的影响。结果:麝香、冰片能显著提高脑缺血-再灌注损伤大鼠神经功能缺损评分,改善其脑组织病理形态,降低脑内COX-2和5-LOX的活性,抑制脑海马组织Cys LT2蛋白表达。结论:麝香、冰片能对抗大鼠脑缺血-再灌注急性期炎性损伤,其机制可能与抑制脑内COX-2与5-LOX的活性有关。
Objective: To investigate the mechanism of Musk and Borneol on cerebral ischemia and reperfusion injury at different time points of acute phase in rats. Methods: 180 rats were divided into seven groups including sham,ischemia-reperfusion after 24 h and72 h model group,Musk 50 and 25 mg / kg groups,Borneol 50 and 25 mg / kg groups,and Xingnaojing 10 m L / kg group. Ischemia-reperfusion model was made after administration of each drug. The neurologic impairment scores at different time points after ischemia and reperfusion was evaluated,activities of cyclooxygenase( COX-2) and 5-lipoxygenase( 5-LOX) in brain tissue were determined,and the expression of Cys LT2 protein and mRNA in hippocampus were explored. Results: Musk and Borneol significantly improved the neurologic impairment scores of ischemia-reperfusion injury rats,improved the pathological morphology of rats brain tissue,reduced the activities of COX-2 and 5-LOX in brain homogenates,and inhibited the expression of Cys LT2 protein in hippocampus. Conclusion: Musk and Borneol have protective effect on inflammatory injury of acute injury in ischemia-reperfusion injury rats,the mechanism is related to inhibition the activity of COX-2 and 5-LOX in brain.