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机构地区:[1]湖南省肿瘤医院重症医学科,湖南长沙410006 [2]湖南省人民医院肾内科,湖南长沙410005 [3]中南大学湘雅二医院心内科,湖南长沙410011
出 处:《医学临床研究》2013年第9期1677-1680,1684,共5页Journal of Clinical Research
摘 要:【目的】观察烟酸对巨噬细胞胆固醇流出的影响并探讨其机制。【方法】对巨噬细胞(raw264.7细胞株)给予不同浓度的烟酸(0~5.0mM)干预24h后,收集细胞,反转录聚合酶链反应测定巨噬细胞三磷酸腺苷结合盒转运体G1(ABCGl),肝X受体a(LxRa)和过氧化物酶增殖物激活受体γ(PPARγ)mRNA表达及Westernblot印迹检测ABCGl和LXRa蛋白表达,采用液体闪烁计数器检测细胞内胆固醇流出。【结果】烟酸呈剂量依赖性增加巨噬细胞ABCGl121RNA及蛋白的表达,并促进其介导的胆固醇流出。LXRa和PPART在巨噬细胞有较高水平的表达,与空白组比较,LXRa,PPART表达在5.0mM浓度的烟酸干预时明显升高。【结论】烟酸可促进巨噬细胞ABCGl介导的胆固醇流出通路,这种作用可能与烟酸上调PPARy和LXRa表达有关。这可为解释烟酸升高高密度脂蛋白胆固醇的机制提供有用的线索。[Objective] To observe the effect of niacin on cholesterol efflux in macrophages, and to explore the possible mechanism. [Methods] Macrophage 264.7 ceils were incubated in the medium containing various concentration of niacin (0-5.0mM) for 24h. Reverse transcription polymerase chain reaction(RT-PCR) was used to determine the expression of adenosine triphosphate-binding cassette transporter G1 (ABCG1), liver X- receptor a(LXRa) and peroxisome proliferator-activated reeeptor-γ(PPARγ), and Western blot was used to detect the protein expression of ABCG1 and LXRa in macrophages. Liquid scintillation counter was used to de- tect cholesterol efflux. [Results]Niacin dose-dependently increased the mRNA and protein expression of AB CG1 and promoted ABCGl-mediated cholesterol efflux in Raw264, 7 ceils. The expression of LXRa and PPARy in Raw264.7 cells was high. Compared with control group, the expression of LXRa and PPAR)' inter- vened by niacin 5.0mM increased obviously. [Conclusion] Niacin can promote cholesterol efflux pathway me- diated by ABCG1, which may be associated with the up-regulation of LXRa and PPAR7 expression. It can provide the clue to explain the mechanisms of high density lipoprotein cholesterol raised by niacin.
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