Terashita Z, Tsushima S, Yoshioka Y, Nomura H, Inada Y, Nishikawa K
Life Sci. 1983 Apr 25;32(17):1975-82. doi: 10.1016/0024-3205(83)90049-8.
CV-3988, rac-3-(N-n-octadecylcarbamoyloxy)-2-methoxypropyl 2-thiazolioethyl phosphate was shown to be a specific inhibitor of platelet activating factor (PAF). This compound in concentrations of 3 x 10(-6) to 3 x 10(-5)M inhibited aggregation of rabbit platelets induced by PAF (3 x 10(-8)M), while it had no effect on the aggregation induced by arachidonic acid, ADP, collagen or A-23187. CV-3988 alone even at a concentration of 10(-3)M had no effect on platelet aggregation. The inhibitory action of CV-3988 on the PAF-induced aggregation was independent of the formation of micelles. The PAF (0.1 to 1.0 micrograms/kg, i.v.)-induced hypotension in anesthetized rats was also inhibited dose-dependently by the i.v. administration of CV-3988 (1 and 10 mg/kg), while the hypotensive actions induced by the i.v. administration of acetylcholine (1 micrograms/kg), arachidonic acid (1 mg/kg), bradykinin (10 micrograms/kg), isoproterenol (1 microgram/kg) and histamine (100 micrograms/kg) were not altered by CV-3988 (10 mg/kg, i.v.). All these findings indicate that CV-3988 specifically inhibits the action of PAF in vitro and in vivo. This is the first report of a PAF antagonist which can specifically inhibit the PAF-induced hypotension as well as the PAF-induced platelet aggregation.
CV - 3988,即消旋 - 3 -(N - 正十八烷基氨甲酰氧基)- 2 - 甲氧基丙基2 - 噻唑啉乙基磷酸酯,被证明是血小板活化因子(PAF)的特异性抑制剂。该化合物浓度在3×10⁻⁶至3×10⁻⁵M时,可抑制PAF(3×10⁻⁸M)诱导的兔血小板聚集,而对花生四烯酸、ADP、胶原或A - 23187诱导的聚集无影响。即使在浓度为10⁻³M时,单独的CV - 3988对血小板聚集也无作用。CV - 3988对PAF诱导的聚集的抑制作用与胶束形成无关。静脉注射PAF(0.1至1.0微克/千克)诱导的麻醉大鼠低血压,也可被静脉注射CV - 3988(1和10毫克/千克)剂量依赖性抑制,而静脉注射乙酰胆碱(1微克/千克)、花生四烯酸(1毫克/千克)、缓激肽(10微克/千克)、异丙肾上腺素(1微克/千克)和组胺(100微克/千克)诱导的低血压不受CV - 3988(10毫克/千克,静脉注射)影响。所有这些发现表明,CV - 3988在体外和体内均特异性抑制PAF的作用。这是关于一种PAF拮抗剂的首次报道,该拮抗剂可特异性抑制PAF诱导的低血压以及PAF诱导的血小板聚集。