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拜阿司匹林对小鼠主动脉核转录因子-κB与基质金属蛋白酶-9表达的调控
引用本文:刘汉华,晏凯利,黄芳,陈娟.拜阿司匹林对小鼠主动脉核转录因子-κB与基质金属蛋白酶-9表达的调控[J].心血管康复医学杂志,2008,17(5):482-484.
作者姓名:刘汉华  晏凯利  黄芳  陈娟
作者单位:湖北省新华医院心内科,湖北,武汉,430015
摘    要:目的:观察拜阿司匹林对小鼠主动脉核转录因子-κB(NF--κB)与基质金属蛋白酶-9(MMP-9)表达的调控作用。方法:40只13周龄小鼠分为拜阿司匹林组(给高脂饲料。拜阿司匹林6mg/kg灌胃),氟伐他汀组(给高脂饲料,氟伐他汀3mg/kg灌胃),模型组(给高脂饲料,生理盐水1ml灌胃),正常对照组(给予普通饲料·生理盐水1ml灌胃),每组10只,17周后,取主动脉,以免疫组化法观察其NF—κB和MMP-9表达的程度。结果:较之对照组模型组,小鼠主动脉粥样斑块的NF--κB与MMP-9表达明显增加,拜阿司匹林组和氟伐他汀组均显著降低其表达(P均〈0.01),拜阿司匹林组和氟伐他汀组间其表达水平无显著差异(P〉0.05)。结论:拜阿司匹林可以降低NF-κB与MMP-9的表达.从而抑制血管内炎症反应和基质纤维蛋白的降解,起到治疗动脉粥样硬化的作用。

关 键 词:阿司匹林  转录因子  基质金属蛋白酶

Effect of β-Aspirin on matrix metalloproteinase-9 and nuclear factor kBp65 expression in aortic artery of atherosclerostic mouse
LIU Han-hua,YAN Kai-li,HUANG Fang,CHEN Juan.Effect of β-Aspirin on matrix metalloproteinase-9 and nuclear factor kBp65 expression in aortic artery of atherosclerostic mouse[J].Chinese Journal of Cardiovascular Rehabilitation Medicine,2008,17(5):482-484.
Authors:LIU Han-hua  YAN Kai-li  HUANG Fang  CHEN Juan
Institution:(Department of Cardiology, Xinhua Hospital of Hubei Province, Wuhan, Hubei, 430015, China)
Abstract:ObjectiveS. To study the effects ofβ--aspirin on expression of matrix metalloproteinase--9 (MMP--9) and nuclear factor κB (NF--κB). Methods.. Forty mouse with the age of thirteen weeks were averagely divided into normal control group, model group, β--aspirin group, fluvastatin group. The mouse of model group, β--aspirin group, fluvastatin group were received the high lipid diet, and the normal control group received the normal diet. In the same time, the β--aspirin group was treated with aspirin intragastric administration 6 mg/kg; the fluvastatin group with fluvastatin intragastric administration 3 mg/kg. Seventeen-week after treatment, expression of MMP--9 and NF--κB in aorta was detected by immunohistochemistry. Results: Compared with normal control group, the expression of MMP --9 and NF--κB significantly increased (P〈0.01) in model group. In β--aspirin group and fluvastatin group the expression of MMP--9 and NF--κB significantly decreased compared with those of model group (P〈0.01). The expression of MMP--9 and NF-κB was no difference between β--aspirin group and the fluvastatin group (P〉0.05) Conclusion. β-- aspirin can inhibits the expression of MMP-- 9 and NF-- κB, so may increases the stability of plaques;
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