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作 者:杨帆[1] 白祥军[1] 刘开俊[1] 杨业金[2] 曾叶[2]
机构地区:[1]华中科技大学同济医学院附属同济医院创伤外科,武汉430030 [2]华中科技大学同济医学院生化与分子生物学系,武汉430030
出 处:《医药导报》2010年第1期9-12,共4页Herald of Medicine
基 金:国家自然科学基金资助项目(基金编号:30070899)
摘 要:目的观察雷公藤内酯醇(TP)对内毒素(LPS)激活小鼠腹腔巨噬细胞(MΦ)分泌促炎递质一氧化氮(NO)和白细胞介素-6(IL-6)的影响。方法分离纯化MΦ,用LPS激活,与不同浓度TP进行培养,以Griess试剂检测培养上清液中的NO含量;以ELISA法检测培养上清液中的IL-6的浓度。结果TP在浓度0.01~10.00μg·mL-1范围内,时间4~24h范围内,对MΦ产生NO具有显著抑制作用(P<0.01),且呈剂量和时间依赖关系;TP在浓度0.001~10.000μg·mL-1范围内,时间12h,对MΦ产生IL-6具有显著抑制作用(P<0.01),呈剂量依赖关系。结论TP可以抑制被LPS激活的MΦ活性,具有高效低毒的抗炎作用。Objective To study the effect of triptolide (TP) on NO and IL-6 of peritoneal elicited macrophage (MФ) activated by lipopolysaccharide(LPS) in mice. Methods The peritoneal elicited macrophage were separated, purified and activated by LPS in mice,then cultured in vitro with a series concentration of TP. The activity of NO and level of IL-6 in cellular supernatants were determined by Griess reagent and ELISA, respectively. Results The activity of NO in MФ was significantly inhibited (P 〈 0.01) by TP(0.01 - 10.00μg·mL^-1) during 4 -24 h in a time and dosage dependent manner;The level of IL-6 was obviously decreased(P 〈 0.01 ) by TP(0. 001 - 10. 000 μg·mL^-1 ) in 12 h in a dose-dependent way. Conclusion TP could inhibit the NO activity and IL-6 level in macrophage activated by LPS, and it has strong anti-inflammatory effects with low toxicity.
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