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机构地区:[1]辽宁医学院附属第一医院老年医学科,锦州121001
出 处:《军医进修学院学报》2012年第11期1160-1163,共4页Academic Journal of Pla Postgraduate Medical School
摘 要:目的研究不同剂量辛伐他汀对氧化型低密度脂蛋白(ox-LDL)诱导的THP-1巨噬细胞胆固醇外流及ATP结合盒受体A1(ABCA1)、CD36表达的影响。方法建立ox-LDL诱导泡沫细胞模型,THP-1巨噬细胞体外培养,用辛伐他汀进行干预,用[3H]标记胆固醇,液体闪烁计数法检测胆固醇外流量,油红O染色观察细胞泡沫化程度,Western Blot、RT-PCR检测细胞内ABCA1及CD36蛋白和mRNA表达。结果辛伐他汀组较ox-LDL诱导组胆固醇外流明显增加,ABCA1受体蛋白及mRNA表达明显增加(P<0.05),同时CD36受体蛋白及mRNA表达明显下调(P<0.05)呈剂量依赖性。结论辛伐他汀可促进ox-LDL诱导的泡沫细胞胆固醇外流,抑制巨噬细胞泡沫化,该作用可能与辛伐他汀上调ABCA1及抑制CD36表达有关。Objective To study the effect of different simvastatin doses on cholesterol efflux induced by oxidized low density lipoprotein(ox-LDL) and expression of ABCA1 and CD36 in THP-1 macrophages.Methods A model of ox-LDL-induced foam cells was established.THP-1 macrophages were cultured in vitro,treated with simavastatin,and labeled with [3H].Cholesterol efflux was measured by liquid scintillation.Formation of foam cells was observed with oil red O staining.Expressions of ABCA1 and CD36 protein and mRNA were detected by Western blot and RT-PCR,respectively.Results The cholesterol efflux volume and the expression level of ABCA1 protein and mRNA were significantly higher while the expression level of CD36 protein and mRNA was significantly lower in simvastatin treatment group than in ox-LDL induction group(P0.05).Conclusion Simvastatin can promote ox-LDL-induced cholesterol efflux from foam cells and inhibit formation of foam macrophages by up-regulating ABCA1 expression and down-regulating CD36 expression.
关 键 词:辛伐他汀 氧化低密度脂蛋白 胆固醇外流 ABCA1 CD36
分 类 号:R543.1[医药卫生—心血管疾病]
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