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1
Interactions of iloprost and sodium nitroprusside on vascular smooth muscle and platelet aggregation.依洛前列素与硝普钠对血管平滑肌及血小板聚集的相互作用。
Br J Pharmacol. 1989 Dec;98(4):1275-80. doi: 10.1111/j.1476-5381.1989.tb12674.x.
2
Interaction of antiplatelet drugs in vitro: aspirin, iloprost, and the nitric oxide donors SIN-1 and sodium nitroprusside.抗血小板药物在体外的相互作用:阿司匹林、伊洛前列素以及一氧化氮供体SIN-1和硝普钠。
Cardiovasc Drugs Ther. 1995 Aug;9(4):619-29. doi: 10.1007/BF00878095.
3
Functional and ligand binding studies suggest heterogeneity of platelet prostacyclin receptors.功能和配体结合研究表明血小板前列环素受体存在异质性。
Br J Pharmacol. 1989 Jul;97(3):657-68. doi: 10.1111/j.1476-5381.1989.tb12001.x.
4
The relaxing activity of iloprost and prostaglandin E2 in the isolated various smooth muscle strips of the rabbit.依洛前列素和前列腺素E2对兔离体不同平滑肌条的舒张活性。
Pharmacology. 1985;31(2):61-6. doi: 10.1159/000138099.
5
Nitric oxide and prostacyclin modulate the alterations in cardiac action potential duration mediated by platelets during ischaemia.一氧化氮和前列环素可调节缺血期间血小板介导的心脏动作电位时程改变。
Cardiovasc Res. 1995 Nov;30(5):788-98.
6
Selective anti-platelet aggregation synergism between a prostacyclin-mimetic, RS93427 and the nitrodilators sodium nitroprusside and glyceryl trinitrate.前列环素类似物RS93427与硝普钠和硝酸甘油等血管扩张剂之间的选择性抗血小板聚集协同作用。
Br J Pharmacol. 1989 Dec;98(4):1296-302. doi: 10.1111/j.1476-5381.1989.tb12677.x.
7
Different roles of endothelium-derived substances on inhibiting platelet aggregation in whole blood.内皮衍生物质在全血中抑制血小板聚集的不同作用。
Gen Pharmacol. 1997 May;28(5):671-3. doi: 10.1016/s0306-3623(96)00368-0.
8
Control of human and animal platelet aggregation by a new prostacyclin analog.
Adv Prostaglandin Thromboxane Leukot Res. 1985;13:363-9.
9
Prostacyclin bioassays using inhibition of platelet aggregation and relaxation of rabbit coeliac artery.使用抑制血小板聚集和兔腹腔动脉舒张的前列环素生物测定法。
J Pharmacol Methods. 1984 Mar;11(1):53-60. doi: 10.1016/0160-5402(84)90052-4.
10
Interaction between NO donors and iloprost in human vascular smooth muscle, platelets, and leukocytes.
J Cardiovasc Pharmacol. 1989;14 Suppl 11:S124-8.

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Functional and molecular characterization of endothelium-dependent and endothelium-independent relaxant pathways in uterine artery of non-pregnant buffaloes.非孕期水牛子宫动脉内皮依赖性和非内皮依赖性舒张途径的功能和分子特征。
Naunyn Schmiedebergs Arch Pharmacol. 2020 Feb;393(2):225-241. doi: 10.1007/s00210-019-01726-y. Epub 2019 Sep 7.
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Eicosanoids, prostacyclin and cyclooxygenase in the cardiovascular system.心血管系统中的类二十烷酸、前列环素和环氧化酶。
Br J Pharmacol. 2019 Apr;176(8):1038-1050. doi: 10.1111/bph.14167. Epub 2018 Apr 14.
3
The anti-aggregating effect of BAY 41-2272, a stimulator of soluble guanylyl cyclase, requires the presence of nitric oxide.BAY 41-2272(一种可溶性鸟苷酸环化酶的刺激剂)的抗聚集作用需要一氧化氮的存在。
Br J Pharmacol. 2010 Nov;161(5):1044-58. doi: 10.1111/j.1476-5381.2010.00943.x.
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The PPAR-Platelet Connection: Modulators of Inflammation and Potential Cardiovascular Effects.PPAR 与血小板的关联:炎症调节剂及潜在心血管效应。
PPAR Res. 2008;2008:328172. doi: 10.1155/2008/328172.
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Interaction of antiplatelet drugs in vitro: aspirin, iloprost, and the nitric oxide donors SIN-1 and sodium nitroprusside.抗血小板药物在体外的相互作用:阿司匹林、伊洛前列素以及一氧化氮供体SIN-1和硝普钠。
Cardiovasc Drugs Ther. 1995 Aug;9(4):619-29. doi: 10.1007/BF00878095.
6
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.
7
Sodium nitroprusside modulates the fibrinolytic system in the rabbit.硝普钠对家兔纤溶系统有调节作用。
Br J Pharmacol. 1990 Nov;101(3):527-30. doi: 10.1111/j.1476-5381.1990.tb14115.x.
8
Effects of zaprinast and rolipram on platelet aggregation and arrhythmias following myocardial ischaemia and reperfusion in anaesthetized rabbits.扎普司特和咯利普兰对麻醉兔心肌缺血再灌注后血小板聚集和心律失常的影响。
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9
The effect of endothelium-derived nitric oxide on ex vivo whole blood platelet aggregation in man.
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10
Effect of prostaglandin E2 and 3-morpholinosydnonimine (SIN-1) on arachidonic acid metabolism in fMLP-stimulated rat neutrophils and on thrombin-induced human platelet aggregation.前列腺素E2和3-吗啉代亚磺酰亚胺(SIN-1)对fMLP刺激的大鼠中性粒细胞中花生四烯酸代谢及凝血酶诱导的人血小板聚集的影响。
Agents Actions. 1992 May;36(1-2):77-82. doi: 10.1007/BF01991232.

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An improved method for washing of human platelets with prostacyclin.一种用前列环素洗涤人血小板的改进方法。
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The interaction of sodium nitroprusside with human endothelial cells and platelets: nitroprusside and prostacyclin synergistically inhibit platelet function.硝普钠与人类内皮细胞和血小板的相互作用:硝普钠与前列环素协同抑制血小板功能。
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Endothelium-dependent vasodilator-and nitrovasodilator-induced relaxation may be mediated through cyclic GMP formation and cyclic GMP-dependent protein phosphorylation.内皮依赖性血管舒张剂和硝基血管舒张剂诱导的舒张作用可能通过环鸟苷酸(cGMP)的形成和环鸟苷酸依赖性蛋白磷酸化介导。
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Evidence for the inhibitory role of guanosine 3', 5'-monophosphate in ADP-induced human platelet aggregation in the presence of nitric oxide and related vasodilators.在一氧化氮及相关血管舒张剂存在的情况下,鸟苷3',5'-单磷酸对二磷酸腺苷诱导的人血小板聚集的抑制作用的证据。
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Comparative pharmacology of EDRF and nitric oxide on vascular strips.内皮舒张因子和一氧化氮对血管条的比较药理学
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Nature. 1987;327(6122):524-6. doi: 10.1038/327524a0.
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The anti-aggregating properties of vascular endothelium: interactions between prostacyclin and nitric oxide.血管内皮的抗聚集特性:前列环素与一氧化氮之间的相互作用。
Br J Pharmacol. 1987 Nov;92(3):639-46. doi: 10.1111/j.1476-5381.1987.tb11367.x.

依洛前列素与硝普钠对血管平滑肌及血小板聚集的相互作用。

Interactions of iloprost and sodium nitroprusside on vascular smooth muscle and platelet aggregation.

作者信息

Lidbury P S, Antunes E, de Nucci G, Vane J R

机构信息

William Harvey Research Institute, St Bartholomew's Hospital Medical College, London.

出版信息

Br J Pharmacol. 1989 Dec;98(4):1275-80. doi: 10.1111/j.1476-5381.1989.tb12674.x.

DOI:10.1111/j.1476-5381.1989.tb12674.x
PMID:2482103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1854807/
Abstract
  1. The aim of the study was to assess and quantify any synergism occurring between the stable analogues of prostacyclin (iloprost) and nitric oxide (sodium nitroprusside) with respect to both relaxation of vascular smooth muscle and inhibition of platelet aggregation in the rabbit. 2. Iloprost (0.3-3 ng ml-1) and sodium nitroprusside (0.3-3 ng ml-1) caused dose-dependent relaxation of the rabbit mesenteric and coeliac arteries. 3. Iloprost (0.3-30 ng ml-1) and sodium nitroprusside (0.03-30 micrograms ml-1) caused dose-dependent inhibition of rabbit platelet aggregation induced by adenosine diphosphate or collagen. 4. In combination, iloprost and sodium nitroprusside caused an inhibition of platelet aggregation that was 2-3 fold greater than would be expected by summation, while no such potentiation was observed on vascular smooth muscle. 5. Thus, our results indicate that under physiological conditions the mediators prostacyclin and endothelium-derived relaxing factor (NO) can exert a synergistic action on platelets, but have only an additive effect on vascular smooth muscle.
摘要
  1. 本研究的目的是评估和量化前列环素(依洛前列素)和一氧化氮(硝普钠)的稳定类似物在兔血管平滑肌舒张和血小板聚集抑制方面所产生的协同作用。2. 依洛前列素(0.3 - 3纳克/毫升)和硝普钠(0.3 - 3纳克/毫升)可引起兔肠系膜动脉和腹腔动脉的剂量依赖性舒张。3. 依洛前列素(0.3 - 30纳克/毫升)和硝普钠(0.03 - 30微克/毫升)可引起对二磷酸腺苷或胶原诱导的兔血小板聚集的剂量依赖性抑制。4. 依洛前列素和硝普钠联合使用时,对血小板聚集的抑制作用比预期的相加作用大2至3倍,而在血管平滑肌上未观察到这种增强作用。5. 因此,我们的结果表明,在生理条件下,介质前列环素和内皮源性舒张因子(一氧化氮)对血小板可发挥协同作用,但对血管平滑肌仅具有相加作用。