摘要
用钙敏感的荧光指示剂Fura-2/Am定量分析大黄素对小鼠腹腔巨噬细胞内(Ca2+)i的影响。结果显示:在巨噬细胞悬液中相继加入不同剂量的CaCl2后,(Ca2+)i明显增高(P<0.01)。巨噬细胞用适当剂量大黄素予处理10min,使用上述不同剂量的CaCl2后,(Ca2+)i水平明显增高,该实验进一步提示;大黄素可促进细胞内Ca2+释放,也可促进细胞外Ca2+内流。而且大黄素对[Ca2+]i的作用呈剂量依赖性。
Effect of Emodin (EMD) on free intracellular Ca2+([Ca2+]i) in peritoneal macrophages of mice was measured with Ca2+ sensitive fluorescent indicator Furi-2/A m quantitatively.Results showed that in the resting, [Ca2+]i level in the peritoneal macrophages was 198.56±44.82nmol/L (n=11) in Ca2+ free Hank's solution. After adding 0.75, 1.75 and 2.75 mmol/L CaCl2 to macrophages suspension sequentially, the free[Ca2+] levels were obviously higher as compared with that of the resting level (P<0.01). When the macrophages were pretreated with adequate doses of EMD for 10 min, in the resting or using the above doses of CaCl2,the[Ca2+] was significantly increased as compared with the contrcl groups (P<0.01).The present investigition indicated that EMD can not only promote the release of intracelular Ca2+ but also the influx of extracellular Ca2+. Furthermore the effect of FMD on [C2+]i is dose dependent.
出处
《中草药》
CAS
CSCD
北大核心
1995年第4期199-200,共2页
Chinese Traditional and Herbal Drugs
基金
国家自然科学基金