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1-O-十六烷基/十八烷基-2-乙酰基-sn-甘油-3-磷酸胆碱(血小板活化因子)对兔血小板磷脂酶的激活作用及血栓素的合成

Activation of rabbit platelet phospholipase and thromboxane synthesis by 1-O-hexadecyl/octadecyl-2-acetyl-sn-glyceryl-3-phosphorylcholine (platelet activating factor).

作者信息

Shaw J O, Klusick S J, Hanahan D J

出版信息

Biochim Biophys Acta. 1981 Jan 26;663(1):222-9. doi: 10.1016/0005-2760(81)90208-3.

Abstract

1-O-Hexadecyl/octadecyl-2-acetyl-sn-glyceryl-3-phosphorylcholine (AGEPC), structurally identical with platelet activating factor, is a potent stimulus for rabbit platelet aggregation and serotonin secretion. AGEPC at concentrations between 10(-10) and 10(-8) M induced stimulation of rabbit platelet synthesis of thromboxane B2. The dose vs. response curve for platelet thromboxane B2 synthesis was displaced slightly towards higher stimulus concentrations compared to [3H]serotonin secretion, with half-maximal concentrations of 2.5 . 10(-9) and 8 . 10(-10) M, respectively. Rates of thromboxane B2 synthesis and secretion were similar with a t 1/2 max of 4.0-4.5 s for both processes. AGEPC induced a decrease in platelet [14C]arachidonic acid in both phosphatidylinositol and phosphatidylcholine, although [14C]arachidonic acid turnover in phosphatidylcholine was not observed below 1 . 10(-8) M AGEPC. Concomitantly, this decrease in phospholipid [14C]arachidonic acid was associated with a marked increase of radiolabel in platelet diacylglycerol and phosphatidic acid 15 s after AGEPC addition, suggesting the possibility of a phospholipase C-diacylglycerol lipase mechanism of fatty acid cleavage. As observed previously with secretion and aggregation, removal of the 2-acetyl group from AGEPC abrogated all capacity of this molecule to stimulate platelet phospholipase. This study indicates that AGEPC (or platelet activating factor) activation of rabbit platelet phospholipase occurs in a time-course and concentration range similar to that required for [3H]serotonin secretion.

摘要

1-十六烷基/十八烷基-2-乙酰基-sn-甘油-3-磷酸胆碱(AGEPC),其结构与血小板活化因子相同,是兔血小板聚集和5-羟色胺分泌的有效刺激物。浓度在10^(-10)至10^(-8) M之间的AGEPC可诱导兔血小板血栓素B2合成增加。与[3H]5-羟色胺分泌相比,血小板血栓素B2合成的剂量-反应曲线向更高刺激浓度方向略有偏移,半最大浓度分别为2.5×10^(-9) M和8×10^(-10) M。血栓素B2的合成和分泌速率相似,两个过程的t 1/2 max均为4.0 - 4.5秒。AGEPC可使磷脂酰肌醇和磷脂酰胆碱中的血小板[14C]花生四烯酸减少,尽管在低于1×10^(-8) M AGEPC时未观察到磷脂酰胆碱中[14C]花生四烯酸的周转。同时,添加AGEPC 15秒后,磷脂[14C]花生四烯酸的这种减少与血小板二酰基甘油和磷脂酸中放射性标记的显著增加相关,提示脂肪酸裂解可能存在磷脂酶C - 二酰基甘油脂肪酶机制。如先前在分泌和聚集实验中所观察到的,从AGEPC上去除2-乙酰基消除了该分子刺激血小板磷脂酶的所有能力。本研究表明,AGEPC(或血小板活化因子)对兔血小板磷脂酶的激活发生的时间进程和浓度范围与[3H]5-羟色胺分泌所需的相似。

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