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机构地区:[1]湖南省人民医院肾内风湿免疫科,湖南长沙410006 [2]中南大学湘雅二医院风湿免疫科,湖南长沙410000
出 处:《中国药业》2014年第14期12-14,共3页China Pharmaceuticals
摘 要:目的研究三甲氧基二苯乙烯(BTM)对小鼠巨噬细胞经脂多糖(LPS)诱导后产生肿瘤坏死因子-α(TNF-α)及细胞核因子-κB(NF-κB)活化的调控作用。方法培养RAW246.7小鼠巨噬细胞,加入不同浓度的BTM或白藜芦醇,再加入LPS活化细胞,收集细胞上清液用L929细胞结晶紫染色法检测TNF-α的活性,制作细胞爬片用免疫细胞化学法检测巨噬细胞中NF-κB的表达。结果BTM和白藜芦醇本身对L929细胞无细胞毒性;经不同浓度BTM和白藜芦醇处理后巨噬细胞产生TNF-α的水平及表达NF-κB的阳性率呈剂量依赖性减少,BTM抑制巨噬细胞产生TNF-α及表达NF-κB的能力大于白藜芦醇,巨噬细胞产生TNF-α的活性及NF-κB的阳性细胞率均与药物浓度呈负相关,TNF-α的活性和NF-κB的阳性细胞率呈正相关。结论BTM和白藜芦醇在浓度为5~80μmol/L范围内,呈浓度依赖性地通过抑制NF-κB的活化来抑制TNF-α的产生,且BTM抑制巨噬细胞产生TNF-α和NF-κB活化的能力犬于白藜芦醇。Objective To study the regulating effects of 3,5,4'-trimethoxystilbene(BTM) on the TNF-α production and the NF-κB activation in murine macrophages activated by LPS. Methods The murine macrophage cell line RAW264. 7 cells were cultured and different concentrations of BTM or resveratrol were added,then LPS activated cells were added. The cellular supernatant was collected for detecting the TNF-α activity by the L929 cell crystal violet staining and the cell climbing slides were prepared for detecting the NF-κB expression in macrophages by immunocytochcmistry method. Results BTM and resveratrol had no cytotoxicity to L929 cells. After processing by different concentrations of BTM and resveratrol, the TNF-α production level and the positive rate of NF-κB expression in macrophages showed the dosedependent decrease. The ability of BTM for inhibiting the TNF-α production level and NF-κB expressing in macrophages was greater than that of resveratrol. The activity of macrophages for producing TNF-α and the positive cell rate of NF-κB were negatively correlated with the drug concentration, while the TNF-α activity was positively correlated with the positive cell rate of NF-κB. Conclusion BTM and resveratrol in the concentration range of 5- 80 μmol/L inhibit TNF-α production with a concentration dependent manner by inhibiting NF-κB activation. The ability of BTM for inhibiting TNF-α production and the NF-κB activation in macrophages is greater than that of resveratrol.
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