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血栓素A2/前列腺素H2激动剂[3H]U46619与洗涤后的人血小板的结合。

Binding of a thromboxane A2/prostaglandin H2 agonist [3H]U46619 to washed human platelets.

作者信息

Liel N, Mais D E, Halushka P V

机构信息

Department of Cell and Molecular Pharmacology and Therapeutics, Medical University of South Carolina, Charleston 29425.

出版信息

Prostaglandins. 1987 Jun;33(6):789-97. doi: 10.1016/0090-6980(87)90107-9.

Abstract

The binding characteristics of [3H]U46619 to washed human platelets were studied. [3H]U46619 binding to washed human platelets was saturable and displaceable. Kinetic studies yielded a Kd of 11 +/- 4 nM (n = 4). Scatchard analysis of equilibrium binding studies revealed one class of high affinity binding sites with a Kd of 20 +/- 7 nM and a Bmax of 9.1 +/- 2.3 fmole/10(7) platelets (550 +/- 141 binding sites per platelet) (n = 4). A number of compounds that act as either agonists or antagonists of the TXA2/PGH2 receptor were tested for their ability to inhibit the binding of [3H]U46619 to washed human platelets. The Kds of the agonists and antagonists were similar to their potencies to induce or inhibit platelet aggregation. These data provide some evidence that [3H]U46619 binds to the putative human platelet TXA2/PGH2 receptor.

摘要

研究了[3H]U46619与洗涤过的人血小板的结合特性。[3H]U46619与洗涤过的人血小板的结合是可饱和且可置换的。动力学研究得出的解离常数(Kd)为11±4 nM(n = 4)。平衡结合研究的Scatchard分析显示存在一类高亲和力结合位点,其Kd为20±7 nM,最大结合容量(Bmax)为9.1±2.3飞摩尔/10^7个血小板(每个血小板有550±141个结合位点)(n = 4)。测试了多种作为血栓素A2/前列腺素H2(TXA2/PGH2)受体激动剂或拮抗剂的化合物抑制[3H]U46619与洗涤过的人血小板结合的能力。激动剂和拮抗剂的Kd与其诱导或抑制血小板聚集的效力相似。这些数据提供了一些证据,表明[3H]U46619与假定的人血小板TXA2/PGH2受体结合。

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