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关于半合成血小板激活因子对人血小板刺激作用的研究。

Studies on the stimulation of human blood platelets by semi-synthetic platelet-activating factor.

作者信息

Ostermann G, Till U, Thielmann K

出版信息

Thromb Res. 1983 Apr 15;30(2):127-36. doi: 10.1016/0049-3848(83)90235-9.

Abstract

"Saturated" and "unsaturated" platelet-activating factor (PAF) obtained from ratfish liver oil were proved to exert potent stimulation on human blood platelets. Using 0.025 to 1.0 mumol/1 PAF a dose-dependent platelet aggregation in platelet-rich plasma was observed. During PAF-induced irreversible aggregation a 9 to 40% release of platelet bound serotonin occurred. The specific effect of PAF, however, seems to be limited to induce reversible aggregation since second wave of aggregation and serotonin release were suppressed by a combination of acetylsalicylic acid and an ADP scavenging system. Incubation of PAF for 30 min in plasma resulted in a 90% loss of its platelet aggregating power. Subthreshold concentrations of PAF enhanced the platelet aggregation triggered by suboptimal concentrations of ADP, epinephrine, or collagen. Vice versa non-aggregating concentrations of ADP, epinephrine, collagen, Ca-ionophore A 23,187, or arachidonic acid amplified PAF-induced platelet aggregation. The synergistic effect of PAF and other stimuli of blood platelet activation can be partly interpreted as a stimulating effect of PAF on the metabolization of arachidonic acid.

摘要

从银鲛鱼肝油中提取的“饱和”和“不饱和”血小板活化因子(PAF)被证明对人血小板有强烈刺激作用。使用0.025至1.0μmol/1的PAF,在富含血小板的血浆中观察到剂量依赖性血小板聚集。在PAF诱导的不可逆聚集中,血小板结合的血清素释放了9%至40%。然而,PAF的特定作用似乎仅限于诱导可逆聚集,因为乙酰水杨酸和ADP清除系统的组合抑制了第二波聚集和血清素释放。PAF在血浆中孵育30分钟导致其血小板聚集能力丧失90%。亚阈值浓度的PAF增强了由次优浓度的ADP、肾上腺素或胶原蛋白引发的血小板聚集。反之,非聚集浓度的ADP、肾上腺素、胶原蛋白、钙离子载体A 23187或花生四烯酸会放大PAF诱导的血小板聚集。PAF与其他血小板活化刺激物的协同作用部分可解释为PAF对花生四烯酸代谢的刺激作用。

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