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首页> 外文期刊>Pharmacology: International Journal of Experimental and Clinical Pharmacology >Berberine Induces CYP2J2 Expression in Human U251 Glioma Cells via Regulation of Peroxisome Proliferator-Activated Receptor Alpha
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Berberine Induces CYP2J2 Expression in Human U251 Glioma Cells via Regulation of Peroxisome Proliferator-Activated Receptor Alpha

机译:Berberine通过调节过氧化物体增殖物激活的受体α在人U251胶质瘤细胞中诱导CYP2J2表达

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摘要

Background: Berberine is a promising natural drug that has a potential therapeutic effect on neurodegenerative diseases. Objectives: Using U251 cells in vitro, we investigated whether berberine exerts its neuroprotective effect via regulation of CYP2J2. Method: After pretreatment with increasing concentrations (1, 3, and 10 mu mol/L) of berberine for 0.5 h, U251 cells were stimulated with 1 mu g/mL of lipopolysaccharide (LPS). Cell viability was measured 24 h later using a CCK8 kit. mRNA and protein levels of CYP2J2 and peroxisome proliferator-activated receptor alpha (PPAR alpha) were measured by quantitative real-time-polymerase chain reaction and western blotting, respectively, after 24 h of exposure to 1, 3, or 10 mu mol/L berberine. Fluorescence immunocytochemistry was also used to evaluate PPAR alpha protein expression after treatment of U251 cells with 10-mu mol/L berberine for 24 h. Transient transfection (cotransfection with the plasmid of PPAR alpha- and RXR alpha -containing) followed by luciferase and chromatin immunoprecipitation assays was used to elucidate the molecular mechanism underlying the observed effects. Results: Compared to the control, LPS-induced U251 cell death was attenuated by berberine in a dose-dependent manner. After 24 h, cell viability was found to be 52.3% (p mol/L berberine treatment, respectively. At these concentrations, berberine increased the CYP2J2 mRNA levels by 1.31-fold (p mRNA levels 1.17-fold (p protein level was also significantly upregulated in U251 cells by berberine (concentrations in 1, 3, and 10 mu mol/L) in a dose-dependent manner, compared with the respective control groups. Further investigation indicated that berberine enhances the heterodimerization of PPAR alpha and RXR alpha, which together bind to the CYP2J2 promoter to induce the expression of CYP2J2 in U251 cells. Conclusion: Upon exposure of U251 cells to berberine, CYP2J2 expression is induced as a result of PPAR alpha stimulation, resulting in a neuroprotective effect.
机译:背景:小檗碱是一种有希望的天然药物,对神经变性疾病具有潜在的治疗作用。目的:在体外使用U251细胞,我们研究了小檗碱是否通过CYP2J2的调节施加其神经保护作用。方法:用浓度的浓度(1,3和10μmmol/l)进行0.5小时进行预处理后,用1μg/ ml脂多糖(LPS)刺激U251细胞。使用CCK8试剂盒以后测量细胞活力。通过定量的实时 - 聚合酶链反应和蛋白质印迹分别通过定量实时 - 聚合酶链反应和蛋白质印迹,在24小时内暴露于1,3或10μmol/ l后测量CYP2J2和过氧化物体增殖剂活化受体α(PPARα)的mRNA和蛋白质水平。小檗碱。荧光免疫细胞化学也用于评估PPARα蛋白表达后用10-mo mol / l小檗24小时处理U251细胞。瞬时转染(具有PPARα-和RXRα-阳离子质粒的COTRANSFETITE),然后用荧光素酶和染色质免疫沉淀测定法来阐明观察到的效果的分子机制。结果:与对照相比,LPS诱导的U251细胞死亡以剂量依赖性方式衰减。 24小时后,发现细胞活力分别为52.3%(P mol / l Berberine治疗。在这些浓度下,Berberine将Cyp2J2 mRNA水平增加1.31倍(P mRNA水平1.17倍(P蛋白质水平也显着显着与各种对照组相比,通过依赖于依赖性方式在U251细胞中上调结合CYP2J2启动子以诱导CYP2J2在U251细胞中的表达。结论:在暴露U251细胞到小檗碱后,由于PPARα刺激而诱导CYP2J2表达,导致神经保护作用。

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