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作 者:卢振华[1] 马业新[1] 冯达应[1] 柯辉[1]
机构地区:[1]华中科技大学同济医学院附属同济医院心内科,湖北省武汉市430030
出 处:《中国动脉硬化杂志》2008年第11期881-884,共4页Chinese Journal of Arteriosclerosis
摘 要:目的观察西洛他唑对兔动脉粥样硬化斑块组织的影响,进一步探讨西洛他唑抗动脉粥样硬化作用及其可能机制。方法将30只新西兰雄性白兔随机分为正常对照组、高脂饮食组和西洛他唑组。酶法检测血脂,免疫沉淀法测定血清C反应蛋白水平,免疫组织化学检测基质金属蛋白酶9和核因子κB的表达,病理形态学分析各组主动脉内膜厚度和斑块面积,逆转录聚合酶链反应检测血管组织单核细胞趋化蛋白1mRNA的表达。结果实验第12周末,西洛他唑组总胆固醇、甘油三酯和低密度脂蛋白胆固醇水平低于高脂饮食组,但高于正常对照组(P均<0.01);西洛他唑组主动脉内膜厚度和斑块面积低于高脂饮食组,但大于正常对照组(P均<0.01);西洛他唑组核因子κB、单核细胞趋化蛋白1和基质金属蛋白酶9的表达弱于高脂饮食组,但强于正常对照组(P均<0.01)。结论西洛他唑有抗动脉粥样硬化作用,其作用机制可能与下调核因子κB、单核细胞趋化蛋白1及基质金属蛋白酶9的表达有关。Aim To observe the effects of Cilostazol on rabbit atherosclerotic plaque and try to illustrate the anti- atherosclerotic mechanism of Cilostazol. Methods Thirty New Zealand male rabbits were randomly divided into normal control group ( n = 10), high-cholesterol group ( n = 10 ) and Cilostazol group ( n = 10 ). The levels of serum total cholesterol (TC), triglyceride (TG) and low density lipoprotein cholesterol (LDLC) were detected by Enzymatic assay,and the level of C-reactive protein (CRP) were detected by immuno-preeipitation; the aortic intimal thickness and plaque area of aorta were measured by pathomorphology; the expression of nuclear factor-KB (NF-KB) and matrix metalloproteinase-9 ( MMP-9 ) was detected with immunohistochemical method, and the expression of monocyte chemoattractant protein-1 ( MCP-1 ) was detected by RT-PCR. Results At the end of 12 weeks, the levels of TC, TG and LDLC in the Cilostazol group were significantly lower than that of high-cholesterol group ( P〈0.01 ), but higher than that of control group ( P〈 0.01 ) ; the aortic plaque area and intimal thickness in the Cilostazol group were significantly lower than that in the high- cholesterol group ( P 〈 0.01 ), but higher than that in the control group ( P 〈 0.01 ) ; the NF-κB, MCP-1 and MMP-9 expression of Cilostazol group were sigffificantly lower than that of high-cholesterol group ( P〈0.01 ) , but higher than that of control group ( P 〈 0.01 ). Conclusion Cilostazol has obvious anti-atherosclerotic effects; reducing the expression of NF-κB, MCP-1 and MMP-9 may be the anti-atherosclerotic mechanism of Cilostazol.
关 键 词:内科学 动脉粥样硬化 西洛他唑 单核细胞趋化蛋白.1 基质金属蛋白酶9
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