Jackson C, Ball J, Peel J, Lawry J, Greaves M, Preston F E
Department of Haematology, Royal Hallamshire Hospital, Sheffield, UK.
Thromb Haemost. 1989 Apr 25;61(2):266-9.
We have examined the in vitro effects of DN 9693 (piperidinylimidazo-quinazolinone) on various aspects of platelet reactivity. Our results are consistent with its known function as a phosphodiesterase inhibitor in that it increased platelet cyclic AMP, particularly in conjunction with an adenylate cyclase stimulator, and exerted a profound inhibitory effect on platelet aggregation responses to a variety of agonists. DN 9693 also inhibited ristocetin-induced platelet agglutination (RIPA). We therefore examined its effect on ristocetin co-factor assays and on the binding of a monoclonal antibody (McAb) to platelet membrane glycoprotein Ib (GPIb). The drug inhibited the binding of the monoclonal antibody in a dose-dependent manner. This suggests an effect of the drug on the platelet surface membrane with reduced expression of GPIb. Our results indicate that in addition to its anticipated inhibitory effect on platelet aggregation, DN 9693 may also inhibit platelet adhesion.
我们研究了DN 9693(哌啶基咪唑喹唑啉酮)对血小板反应性各个方面的体外作用。我们的结果与其作为磷酸二酯酶抑制剂的已知功能一致,即它增加了血小板环磷酸腺苷(cAMP),特别是与腺苷酸环化酶刺激剂联合使用时,并对血小板对多种激动剂的聚集反应产生了深远的抑制作用。DN 9693还抑制了瑞斯托霉素诱导的血小板凝集(RIPA)。因此,我们研究了其对瑞斯托霉素辅因子测定以及单克隆抗体(McAb)与血小板膜糖蛋白Ib(GPIb)结合的影响。该药物以剂量依赖性方式抑制单克隆抗体的结合。这表明该药物对血小板表面膜有影响,导致GPIb表达减少。我们的结果表明,除了对血小板聚集的预期抑制作用外,DN 9693还可能抑制血小板黏附。