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1
Human blood platelet behaviour after inhibition of thromboxane synthetase.血栓素合成酶抑制后人类血小板的行为
Br J Clin Pharmacol. 1983;15 Suppl 1(Suppl 1):31S-37S. doi: 10.1111/j.1365-2125.1983.tb02104.x.
2
Effects of dazoxiben and low-dose aspirin on platelet behaviour in man.达唑氧苯和小剂量阿司匹林对人体血小板行为的影响。
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3
Effects of a thromboxane synthetase inhibitor and a cAMP phosphodiesterase inhibitor, singly and in combination, on platelet behaviour.血栓素合成酶抑制剂和环磷酸腺苷磷酸二酯酶抑制剂单独及联合应用对血小板行为的影响。
Thromb Haemost. 1986 Jun 30;55(3):305-8.
4
Lag-phase of arachidonic acid-induced secretion in responders and non-responders to the thromboxane-synthetase inhibitors: involvement of cyclic-AMP.对血栓素合成酶抑制剂有反应者和无反应者中花生四烯酸诱导分泌的延迟期:环磷酸腺苷的作用。
Thromb Res. 1984 Jul 1;35(1):91-7. doi: 10.1016/0049-3848(84)90316-5.
5
Thromboxane synthetase inhibitors differentially antagonize thromboxane receptors in vascular smooth muscle.血栓素合成酶抑制剂对血管平滑肌中的血栓素受体具有不同的拮抗作用。
Naunyn Schmiedebergs Arch Pharmacol. 1981 Dec;318(2):130-4. doi: 10.1007/BF00508837.
6
Effects of thromboxane synthetase inhibition on arachidonate metabolism and platelet behaviour.血栓素合成酶抑制对花生四烯酸代谢及血小板行为的影响。
Br J Clin Pharmacol. 1983;15 Suppl 1(Suppl 1):23S-29S. doi: 10.1111/j.1365-2125.1983.tb02103.x.
7
Pharmacologic inhibition of thromboxane synthetase and platelet aggregation: modulatory role of cyclooxygenase products.血栓素合成酶的药理抑制作用与血小板聚集:环氧化酶产物的调节作用
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8
Thromboxane synthase inhibition potentiates washed platelet activation by endogenous and exogenous arachidonic acid.血栓素合酶抑制作用可增强内源性和外源性花生四烯酸对洗涤血小板的激活作用。
Biochem Pharmacol. 1985 Apr 15;34(8):1151-6. doi: 10.1016/0006-2952(85)90488-5.
9
Effects of heparin on platelet aggregation and release and thromboxane A2 production.肝素对血小板聚集、释放及血栓素A2生成的影响。
Am J Pathol. 1981 Aug;104(2):132-41.
10
Effects of a selective inhibitor of thromboxane synthetase on human blood platelet behaviour.血栓素合成酶选择性抑制剂对人血小板行为的影响。
Thromb Res. 1980 Oct 15;20(2):219-30. doi: 10.1016/0049-3848(80)90387-4.

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Nat Rev Cardiol. 2009 May;6(5):365-73. doi: 10.1038/nrcardio.2009.13. Epub 2009 Apr 14.
2
Inhibition of platelet aggregation by transdermal glyceryl trinitrate.经皮硝酸甘油对血小板聚集的抑制作用。
Br Heart J. 1994 Dec;72(6):575-9. doi: 10.1136/hrt.72.6.575.

本文引用的文献

1
Effects of a selective inhibitor of thromboxane synthetase on human blood platelet behaviour.血栓素合成酶选择性抑制剂对人血小板行为的影响。
Thromb Res. 1980 Oct 15;20(2):219-30. doi: 10.1016/0049-3848(80)90387-4.
2
3-(1-imidazolylmethyl) indoles: potent and selective inhibitors of human blood platelet thromboxane synthetase.3-(1-咪唑基甲基)吲哚:人血小板血栓素合成酶的强效选择性抑制剂。
Agents Actions. 1981 May;11(3):274-80. doi: 10.1007/BF01967626.
3
Inhibition of platelet thromboxane synthesis by 7-(1-imidazolyl) heptanoic acid: dissociation from inhibition of aggregation.7-(1-咪唑基)庚酸对血小板血栓烷合成的抑制作用:与聚集抑制作用的解离
Thromb Res. 1981 Nov 15;24(4):307-17. doi: 10.1016/0049-3848(81)90004-9.
4
Prolongation of rat tail bleeding time caused by oral doses of a thromboxane synthetase inhibitor which have little effect on platelet aggregation.口服剂量的血栓素合成酶抑制剂可延长大鼠尾部出血时间,而该抑制剂对血小板聚集几乎没有影响。
Thromb Haemost. 1982 Feb 26;47(1):46-9.
5
Thromboxane synthetase inhibition as antithrombotic strategy.抑制血栓素合成酶作为抗血栓形成策略。
Lancet. 1981 May 16;1(8229):1073-5. doi: 10.1016/s0140-6736(81)92241-8.
6
Inhibition of thromboxane synthetase does not necessarily prevent platelet aggregation.抑制血栓素合成酶不一定能防止血小板聚集。
Lancet. 1981 May 9;1(8228):1057-8. doi: 10.1016/s0140-6736(81)92224-8.
7
The effect of salicylates on the hemostatic properties of platelets in man.水杨酸盐对人体血小板止血特性的影响。
J Clin Invest. 1968 Sep;47(9):2169-80. doi: 10.1172/JCI105903.
8
Inhibition of adenosine diphosphate-induced secondary aggregation and other platelet functions by acetylsalicylic acid ingestion.摄入乙酰水杨酸对二磷酸腺苷诱导的继发性聚集及其他血小板功能的抑制作用。
Proc Soc Exp Biol Med. 1968 Feb;127(2):547-51. doi: 10.3181/00379727-127-32737.
9
A comparison of an effect of different anti-inflammatory drugs on human platelets.不同抗炎药物对人体血小板作用的比较。
J Clin Pathol. 1970 Sep;23(6):522-5. doi: 10.1136/jcp.23.6.522.
10
Isolation and structure of two prostaglandin endoperoxides that cause platelet aggregation.两种引起血小板聚集的前列腺素内过氧化物的分离与结构
Proc Natl Acad Sci U S A. 1974 Feb;71(2):345-9. doi: 10.1073/pnas.71.2.345.

血栓素合成酶抑制后人类血小板的行为

Human blood platelet behaviour after inhibition of thromboxane synthetase.

作者信息

Heptinstall S, Fox S C

出版信息

Br J Clin Pharmacol. 1983;15 Suppl 1(Suppl 1):31S-37S. doi: 10.1111/j.1365-2125.1983.tb02104.x.

DOI:10.1111/j.1365-2125.1983.tb02104.x
PMID:6401998
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1427694/
Abstract

1 We have determined the extent to which sodium arachidonate (NaAA) induces a release reaction in platelet-rich plasma (PRP) from different individuals and have studied the ability of the thromboxane synthetase inhibitor UK 34787 to modify this release. We have also determined the extent of the platelet release reaction induced in PRP from different individuals by preparations of platelet-derived thromboxane A2 (TXA2). 2 The release of [14C]-serotonin induced by NaAA is more extensive in PRP from some individuals than from others. 3 There is a direct relation between the extent of the release reaction induced in different PRPs by NaAA and TXA2. 4 UK 34787 prevents the NaAA-induced release reaction in PRP from some individuals ("responders") but not in PRP from others ("non-responders"). 5 The mean extent of the NaAA-induced release reaction for the "non-responders" was significantly higher than that for the "responders" even in the absence of UK 34787, but there was some overlap between the individual results. 6 Platelets from "responders" and "non-responders" did not differ in the amount of malondialdehyde (MDA) produced or in the effectiveness with which UK 34787 inhibited MDA production. 7 Platelet-derived TXA2 from "responders" and "non-responders" did not have markedly different effects when tested in a single preparation of PRP.

摘要
  1. 我们已经确定了花生四烯酸钠(NaAA)在不同个体的富血小板血浆(PRP)中诱导释放反应的程度,并研究了血栓素合成酶抑制剂UK 34787改变这种释放的能力。我们还确定了血小板衍生的血栓素A2(TXA2)制剂在不同个体的PRP中诱导的血小板释放反应的程度。2. NaAA诱导的[14C] - 血清素释放在一些个体的PRP中比在其他个体中更广泛。3. NaAA和TXA2在不同PRP中诱导的释放反应程度之间存在直接关系。4. UK 34787可防止NaAA诱导的一些个体(“反应者”)的PRP中的释放反应,但不能防止其他个体(“无反应者”)的PRP中的释放反应。5. 即使在没有UK 34787的情况下,“无反应者”的NaAA诱导的释放反应的平均程度也显著高于“反应者”,但个体结果之间存在一些重叠。6. “反应者”和“无反应者”的血小板在产生的丙二醛(MDA)量或UK 34787抑制MDA产生的有效性方面没有差异。7. 在单一的PRP制剂中进行测试时,“反应者”和“无反应者”的血小板衍生的TXA2没有明显不同的作用。