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作 者:张颖[1] 张燕堂[2] 郑文[3] 岳雯[4] 晏子超 王家富[4] 商战平[4]
机构地区:[1]泰山医学院放射学院,泰安271016 [2]泰山医学院校医院,泰安271016 [3]山东省交通医院检验科,济南250031 [4]泰山医学院病理生理学教研室,泰安271016
出 处:《中药药理与临床》2012年第6期32-35,共4页Pharmacology and Clinics of Chinese Materia Medica
基 金:泰山医学院青年基金资助项目(No.2010ZRQN046);泰安市科技局资助项目(No.20123062)
摘 要:目的:探讨二苯乙烯苷(TSG)对血管内皮细胞在溶血性磷脂酰胆碱(LPC)诱导下的保护作用及其机制。方法:体外培养人脐静脉血管内皮细胞(HUVECs),将TSG以10.0;1.0;0.1mol/L预先作用于HUVECs 1小时后,继续培养,再给予10mg/L的LPC作用于HUVECs共同孵育24小时,检测细胞的存活率、MDA、NO和ROS的变化。结果:以10mg/L浓度LPC的模型组与对照组比较结果显示,观测到细胞培养上清液中MDA含量显著性增加,而细胞培养上清液中NO含量明显降低,细胞的活性氧水平有所增加,细胞的存活率降低。实验组与模型组比较发现,以0.1μmol/L作为起效剂量,在0.1~10.0μmol/L浓度的范围内有效,并具有一定的浓度依赖关系。随着药物有效浓度的增加,细胞培养上清液中MDA含量显著性降低,NO含量显著性升高,细胞的活性氧水平则降低和细胞的存活率却显著性升高。结论:二苯乙烯苷能够通过抑制活性氧水平,增加NO的生成,增加细胞的存活,从而对LPC损伤的血管内皮细胞发挥保护作用。To observe the protection of 2,3,4, 5-tetrahydroxystilbene- 2-O-J3-D glueoside (TSG) agaist Lysophosphatidylehdine (LPC)- induced vascular endothelial cell injury and the effect of TSG on Malefic Dialdehyde ( MDA), NO, and apoptosis. Methods: The third and fourth generation of human umbilical vein endothelial cells (HUVECs), which were cultured in vitro and propagated, were used in the experi- ment. The cells were randomly divided into three groups: the control group; the modal group (TSG) ; the experimental group (TSG + LPC). The blank group was not adminidtered with any reagent. To establish Group TSG, LPC was administered to HUVECs on the basis of 10mg/L and in- cubated with the cells for 24h to induce endothelial cell injury; To establish Group TSG + LPC, TSG was administered to HUVECs on the basis of 10.0, 1.0, 0. 1 p. mol / L lh before LPC was administered on the basis of 10mg/L and then the cells were incubated for 24h. Nexfly, the cell viability, ADMA, NO, and apeptosis rate were detected separately. Results: Compared with that of the control group, the cell culture su- pernatant of Group TSG + LPC had significantly increased MDA and ROA while notably decreased NO and increased apoptosis as well as re- duced cell viability. Then compared with the Lt~ injury group, Group TSG + LPC had significantly decreased MDA and ROS while notably in- creased NO and decreased apoptosis as well as remarkably elevated cell viability in the cell culture supernatant. Conclusion: Stilbene glyco- sides may protect LPC-injured vascular endothelial cells by inhibiting the expression of ADMA, enhancing NO production and meanwhile inhibi- ting apoptosis and increasing ceLl survival rate.
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