摘要
目的:研究川芎嗪对花生四烯酸(160μmol/L)诱导的血管内皮细胞损伤和凋亡的保护作用及其机制。方法:MTT法检测细胞存活率,比色法测LDH释放率和细胞MDA含量Hoechst33258荧光染色观察细胞核形态变化并测定凋亡率,琼脂糖凝胶电泳检测DNA降解。结果:川芎嗪(0.25～1.00mmol/L)能浓度依赖性抑制花生四烯酸引起的细胞存活率下降(t=2.52～3.14,P<0.05),并降低细胞LDH释放率和MDA含量(t=3.27～5.88和t=4.64～7.41,P<0.05)。花生四烯酸处理24h后的细胞呈现典型的凋亡核固缩表现,凝胶电泳显示DNA凋亡梯带。川芎嗪(0.25～1.00mmol/L)能降低其凋亡率。结论:川芎嗪对花生四烯酸引起的内皮细胞损伤和凋亡具有保护作用其机制可能与其抗脂质过氧化作用有关。
AIM:To study the protective effects and mechanism of Ligustrazine against damage and apoptosis in human umbilical vascular endothelial cells(HUVECs) induced by 160 μmol/L arachidonic acid(AA). METHODS:The survival rate of cells was detected by MTT,the release rate of lactate dehydrogenase(LDH) and malondialdehyde(MDA)content in endothelial cells(EC) are measured by colorimetric assay.Hoechst 33258 fluorescence staining was used to observe morphological changes of nucleus and determine apoptotic ratio.Agarose gel electrophoresis was used to detect DNA fragmentation. RESULTS:MP(0.25-1.0 mmol/L) prevented the inhibitory effect of viability induced by AA(t=2.52-3.14,P< 0.05).TMP(0.25-1.0 mmol/L) partly prevented the increase in the release rate of LDH and MDA contents induced by AA(t=3.27-5.88,t=4.64-7.41,P< 0.05).Cells treated with 160 μmol/L AA showed typical morphological changes of apoptosis.A 'DNA ladder'was also observed.TMP(0.25-1.0 mmol/L) partly decreased the ratio of apoptotic cells.
出处
《中国临床康复》
CSCD
2003年第30期4066-4067,共2页
Chinese Journal of Clinical Rehabilitation
基金
湖北省教委资助项目(99A060)~~
关键词
川芎嗪
花生四烯酸
血管内皮细胞
细胞凋亡
保护作用
脂质过氧化
TMP can protect AA induced apoptosis in EC and the mechanism of its action may be related to anti lipid peroxidation.
