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前列环素(PGI2)对兔静脉注射血小板活化因子(PAF)所致中性粒细胞减少的抑制作用。

Inhibitory effect of prostacyclin (PGI2) on neutropenia induced by intravenous injection of platelet-activating-factor (PAF) in the rabbit.

作者信息

Camussi G, Tetta C, Bussolino F

出版信息

Prostaglandins. 1983 Mar;25(3):343-51. doi: 10.1016/0090-6980(83)90037-0.

Abstract

Intravenous injection into rabbits of 1-O-octadecyl-2-acetyl-sn-glyceryl-3-phosphorylcholine (synthetic Platelet-Activating Factor (PAF)) or PAF derived from rabbit basophils caused acute thrombocytopenia and neutropenia which was consequent to the formation of intravascular polymorphonuclear neutrophil (PMN) aggregates and to their sequestration in the microvasculature, primarily of the lung. Infusion of prostacyclin (PGI2; 10 ng/Kg/min to 50 ng/Kg/min) inhibited in a dose-dependent manner PAF-induced thrombocytopenia and neutropenia as well as the sequestration of PMN in the pulmonary capillary network.

摘要

给兔子静脉注射1-O-十八烷基-2-乙酰基-sn-甘油-3-磷酸胆碱(合成血小板活化因子(PAF))或源自兔嗜碱性粒细胞的PAF,会导致急性血小板减少和中性粒细胞减少,这是由于血管内多形核中性粒细胞(PMN)聚集体的形成及其在主要是肺部的微血管系统中的滞留所致。输注前列环素(PGI2;10 ng/Kg/分钟至50 ng/Kg/分钟)以剂量依赖性方式抑制PAF诱导的血小板减少和中性粒细胞减少以及PMN在肺毛细血管网络中的滞留。

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