Radomski M W, Palmer R M, Read N G, Moncada S
Wellcome Research Laboratories, Kent, U.K.
Thromb Res. 1988 May 15;50(4):537-46. doi: 10.1016/0049-3848(88)90202-2.
Nitric oxide (NO) was compared with prostacyclin as an inhibitor of the activation of human platelets during isolation, washing and storage. The use of NO throughout the procedure prevented the activation of platelets. The morphology and behaviour of NO-washed platelets was similar to that of prostacyclin-washed platelets when stored at 4 degrees C for up to 24 h. Prolonged storage resulted in deterioration of the platelets which occurred earlier in the NO-washed than in the prostacyclin-washed platelets. The protective effect of NO was potentiated by the selective cGMP phosphodiesterase inhibitor M & B 22948, suggesting that it is mediated by the activation of guanylate cyclase.
在人血小板的分离、洗涤和储存过程中,将一氧化氮(NO)与前列环素作为血小板激活抑制剂进行了比较。在整个过程中使用NO可防止血小板激活。当在4℃下储存长达24小时时,经NO洗涤的血小板的形态和行为与经前列环素洗涤的血小板相似。长时间储存会导致血小板恶化,经NO洗涤的血小板比经前列环素洗涤的血小板更早出现这种情况。选择性cGMP磷酸二酯酶抑制剂M&B 22948可增强NO的保护作用,这表明其作用是由鸟苷酸环化酶的激活介导的。