Oelz O, Oelz R, Knapp H R, Sweetman B J, Oates J A
Prostaglandins. 1977 Feb;13(2):225-34. doi: 10.1016/0090-6980(77)90004-1.
Formation of prostaglandin D2 (PGD2) during the aggregation of platelets was determined, employing a specific bioassay. PGD2 was synthesized in human platelet rich plasma (PRP) in response to thrombin, collagen and epinephrine. Indomethacin pretreatment abolished the biosynthesis of PGD2. When thrombin treated PRP was incubated for different periods of time and denatured in the presence of SnCl2 to prevent the formation of PGD2 from endoperoxides during the extraction procedure, PGD2 formation was noted within the first minute of incubation and reached a peak level after 4 minutes. PGD2 from thrombin stimulated PRP was conclusively identified by gas chromatography-mass spectrometry. The formation of PGD2 during platelet aggregation could represent a mechanism of feedback inhibition of aggregation.
采用特定生物测定法测定血小板聚集过程中前列腺素D2(PGD2)的形成。PGD2在富含人血小板的血浆(PRP)中响应凝血酶、胶原蛋白和肾上腺素而合成。吲哚美辛预处理可消除PGD2的生物合成。当凝血酶处理的PRP在不同时间段孵育,并在SnCl2存在下变性以防止在提取过程中由内过氧化物形成PGD2时,在孵育的第一分钟内就注意到PGD2的形成,并在4分钟后达到峰值水平。通过气相色谱-质谱法最终鉴定了来自凝血酶刺激的PRP的PGD2。血小板聚集过程中PGD2的形成可能代表一种聚集反馈抑制机制。