节点文献
木香倍半萜的体外抗炎活性及构效关系研究
In vitro Anti-inflammatory Effects and SAR Studies of Sesquiterpene from Aucklandia lappa Decne.
【Author】 Feng Zhao, Hui Xu, Ming-Hao Zhang, Ke Liu Department of Medicinal Chemistry, School of Pharmacy, Yantai University, Yantai 264005
【机构】 烟台大学药学院天然药物化学教研室;
【摘要】 目的:考察木香倍半萜对LPS诱导的小鼠巨噬细胞释放NO的抑制活性,并探讨其构效关系。方法;采用LPS诱导小鼠巨噬细胞RAW 264.7释放NO,用Griess法测定木香提取物及木香倍半萜对LPS诱导的小鼠巨噬细胞释放NO的抑制率,用MTT法评价细胞毒性。结果:木香石油醚层和乙酸乙酯层提取物对活化的小鼠巨噬细胞释放NO具有明显的抑制作用,IC50分别为 0.10μg/ml和0.86 μg/ml。木香倍半萜对小鼠巨噬细胞释放NO的抑制活性和化学结构之间存在一定的构效关系规律,内酯环及环外双键对于木香倍半萜的NO释放抑制活性具有重要的意义。
【Abstract】 Objective: To evaluate the inhibitory activities of sesquiterpenes from Aucklandia lappa on LPS-induced NO release of mouse macrophage, and study the relationship between the chemical structures and the inhibitory activities. Methods: Determine the quantity of NO by Griess assay and calculate the inhibitory rate of NO release in mouse macrophage RAW 264.7. Evaluate the cytotoxicity by MTT method. Results: The petrol, EtOAc soluble fraction of Aucklandia lappa significantly inhibited NO release induced by LPS, IC50 values are 0.10 μg/ml and 0.86 μg/ml, respectively. Some revelation between the chemical structures and the NO release inhibitory activities were found, the lactone group is seemed to be very important for the NO release inhibitory activity.
【Key words】 Aucklandia lappa Decne.; sesquiterpene; LPS; NO; anti-inflammatory activity; SAR.;
- 【会议录名称】 创新药物及新品种研究、开发学术研讨会论文集
- 【会议名称】创新药物及新品种研究、开发学术研讨会
- 【会议时间】2006-08
- 【会议地点】中国山东烟台
- 【分类号】R284;R285
- 【主办单位】中国药学会抗生素专业委员会、烟台大学药学院、中国新药杂志、中国处方药杂志