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首页> 外文期刊>Cell biochemistry and biophysics >2,3,4′,5-Tetrahydroxystilbene-2-O-β-D-glucoside Suppresses Expression of Adhesion Molecules in Aortic Wall of Dietary Atherosclerotic Rats and Promonocytic U937 Cells
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2,3,4′,5-Tetrahydroxystilbene-2-O-β-D-glucoside Suppresses Expression of Adhesion Molecules in Aortic Wall of Dietary Atherosclerotic Rats and Promonocytic U937 Cells

机译:2,3,4',5-四羟基sti-2-O-β-D-葡萄糖苷抑制饮食性动脉粥样硬化大鼠和原代单核U937细胞主动脉壁黏附分子的表达

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We sought to investigate whether TSG suppressed the ICAM-1/VCAM-1 expression in dietary atherosclerotic rats and in Ox-LDL-induced U937 cells. For this purpose, 60 male Sprague-Dawley rats were randomly-and-equally divided into six groups. Atherosclerosis was induced by feeding rats a hyperlipidemic diet. TSG (120, 60 or 30 mg/kg/day) was administered by oral gavage. Simvastatin (2 mg/kg/day) was administered as positive control whereas physiological saline (0.9 % NaCl) served as untreated control. After 12 weeks, rats were euthanized by ethyl carbonate (1,200 mg/kg) and aortic wall samples were collected. Besides, U937 cells were stimulated for 48 h by Ox-LDL (80 μg/mL) with and without TSG (120, 60, 30 μg/L) or simvastatin (100 μg/L). ICAM-1/VCAM-1 mRNA expression was determined by RT-PCR and protein expression was detected by immunohistochemistry and/or western blotting. The data show that ICAM-1/VCAM-1 mRNA/protein expression was significantly enhanced in atherosclerotic aortas compared with normal diet group. Ox-LDL-induced ICAM-1/VCAM-1 mRNA/protein expression in U937 cells. Importantly, TSG significantly inhibited ICAM-1/VCAM-1 expression in atherosclerotic aortas in a dose-dependent manner. TSG-pretreatment also inhibited ICAM-1/VCAM-1 expression in Ox-LDL-induced U937 cells. Therefore, we concluded that TSG suppressed the expression of adhesion (ICAM-1/VCAM-1) molecules both in vivo (in aortic wall of dietary atherosclerotic rats) and in vitro (U937 cells).
机译:我们试图调查TSG是否抑制饮食动脉粥样硬化大鼠和Ox-LDL诱导的U937细胞中ICAM-1 / VCAM-1的表达。为了这个目的,将60只雄性Sprague-Dawley大鼠随机等分分成六组。通过给大鼠喂高脂饮食来诱发动脉粥样硬化。通过口服管饲法给予TSG(120、60或30 mg / kg /天)。辛伐他汀(2 mg / kg /天)作为阳性对照,而生理盐水(0.9%NaCl)作为未处理的对照。 12周后,将大鼠用碳酸乙酯(1200 mg / kg)安乐死,并收集主动脉壁样品。此外,在有或没有TSG(120、60、30μg/ L)或辛伐他汀(100μg/ L)的条件下,Ox-LDL(80μg/ mL)刺激U937细胞48小时。通过RT-PCR确定ICAM-1 / VCAM-1的mRNA表达,并通过免疫组织化学和/或蛋白质印迹法检测蛋白表达。数据显示,与正常饮食组相比,动脉粥样硬化主动脉中ICAM-1 / VCAM-1 mRNA /蛋白质表达显着增强。 Ox-LDL诱导的U937细胞中ICAM-1 / VCAM-1 mRNA /蛋白质表达。重要的是,TSG以剂量依赖的方式显着抑制动脉粥样硬化主动脉中ICAM-1 / VCAM-1的表达。 TSG预处理还抑制了Ox-LDL诱导的U937细胞中ICAM-1 / VCAM-1的表达。因此,我们得出的结论是,TSG在体内(在饮食动脉粥样硬化大鼠的主动脉壁中)和体外(U937细胞)都抑制了粘附分子(ICAM-1 / VCAM-1)的表达。

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