摘要
目的:探讨Ca2+在SJAMP诱导血小板聚集中的作用。方法:以Fura-2为钙荧光探针,应用双波长法测定了SJAMP对血小板胞内游离钙水平的影响。结果:发现SJAMP在100μg/ml时对血小板胞浆游离钙的影响最为显著,可使正常人血小板胞内钙水平从71.30±7.66nmol/L升至93.96±10.24nmol/L(n=10),在胞外存在1mmol/LCa2+时,SJAMP引起胞内游离钙升高幅度更大.可达116.72±10.66nmol/L(n=10)。另一方面,SJAMP对血小板胞内游离钙的影响,与其它诱导剂相比,其升高幅度较小且时限较长,同时如果血小板预先与环氧化酶抑制剂孵育.则SJAMP对血小板胞内钙的升高作用明显受抑。结论:推测SJAMP对血小板胞内钙的影响可能是一花生四烯酸及其代谢物有关的过程。
Using the method of dual-wavelength measurement of platelet (Ca2+)iand Fura-2 as the Ca2+ fluorophore probe, we measured the effect of Acidic Mu-copolysaccharide from Sticopus Japonicus Selenka (SJAMP) on platelet [Ca2-] i.The results showed that the most significant increase in plate1ets [Ca2+)i was seenwhen the concentration of SJAMP was 100 μg/ml and the elevation of normalplatelet [Ca2 +]i was 93. 96±10. 24 nmol/L, (n = 1O). In the presence of extracellular Ca2+ (1 mmol/L),the magnitude of platelets [Ca2+]i could reach 116. 72±10. 66nmol/I, (n=10). On the other hand,the magnitude of increased platelets [Ca2- ]ireaching the highest level was longer when compared with other platelet aggregationagents. In the mean time.if platelets was first incubated with cyclo-oxygenase inhibitor, the rise of (Ca2+]i evoked by SJAMP was inhibited. The results indlcatedthat the mechanism of the rise of [Ca2+]i induced by SJAMP might be dependentupon the generation of prostaglandin endperoxides and/or TXA2
出处
《临床血液学杂志》
CAS
1999年第1期5-7,共3页
Journal of Clinical Hematology
基金
国家自然科学基金!39370322