兔体内前列环素（PGI2）的肝脏代谢：一种强效新型血小板聚集抑制剂的形成。 - Suppr

Suppr

超能文献

Hepatic metabolism of prostacyclin (PGI2) in the rabbit: formation of a potent novel inhibitor of platelet aggregation.

作者信息

Wong P Y, Malik K U, Desiderio D M, McGiff J C, Sun F F

出版信息

Biochem Biophys Res Commun. 1980 Mar 28;93(2):486-94. doi: 10.1016/0006-291x(80)91103-1.

DOI:10.1016/0006-291x(80)91103-1

PMID:6992772

Abstract

摘要

相似文献

Hepatic metabolism of prostacyclin (PGI2) in the rabbit: formation of a potent novel inhibitor of platelet aggregation.兔体内前列环素（PGI2）的肝脏代谢：一种强效新型血小板聚集抑制剂的形成。

Biochem Biophys Res Commun. 1980 Mar 28;93(2):486-94. doi: 10.1016/0006-291x(80)91103-1.

6-keto PGE1: a possible metabolite of prostacyclin having platelet antiaggregatory effects.6-酮前列环素E1：一种可能具有血小板抗聚集作用的前列环素代谢产物。

Hypertension. 1980 Jul-Aug;2(4):524-8. doi: 10.1161/01.hyp.2.4.524.

Metabolism of prostacyclin: formation of an active metabolite in the liver.前列环素的代谢：肝脏中活性代谢产物的形成。

Fed Proc. 1981 May 15;40(7):2001-4.

Heparin-mediated neutralization of platelet antiaggregatory activity of prostacyclin (PGI2): studies on mechanism.肝素对前列环素（PGI2）血小板抗聚集活性的中和作用：作用机制研究

Am J Hematol. 1985 Oct;20(2):97-105. doi: 10.1002/ajh.2830200202.

Prostacyclin is the major prostaglandin released from the isolated perfused rabbit and rat heart.前列环素是从离体灌注的兔和大鼠心脏释放的主要前列腺素。

Nature. 1977 Jul 14;268(5616):160-3. doi: 10.1038/268160a0.

Metabolism of prostacyclin in the rabbit kidney.前列环素在兔肾中的代谢

J Biol Chem. 1979 Jan 10;254(1):12-4.

Prostacyclin (PGI2) activity in rat kidney-stimulated by angiotensin II.前列环素（PGI2）在大鼠肾脏中的活性受血管紧张素II刺激。

Exp Mol Pathol. 1979 Apr;30(2):242-54. doi: 10.1016/0014-4800(79)90057-1.

Anti-aggregatory effect of prostacyclin (PGI2) in vivo.前列环素（PGI2）在体内的抗聚集作用。

Br J Pharmacol. 1979 May;66(1):10-2. doi: 10.1111/j.1476-5381.1979.tb16090.x.

Reduced platelet aggregation by pentoxifylline stimulated prostacyclin release.己酮可可碱刺激前列环素释放，从而降低血小板聚集。

Vasa. 1981;10(3):249-52.

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.

引用本文的文献

Profiling of arachidonic acid metabolites in rabbit platelets by radio gas chromatography.用放射性气相色谱法分析兔血小板中花生四烯酸代谢物

Lipids. 1993 Apr;28(4):361-4. doi: 10.1007/BF02536324.

Stimulation of renin release by 6-oxo-prostaglandin E1 and prostacyclin.6-氧代前列腺素E1和前列环素对肾素释放的刺激作用。

Br J Pharmacol. 1982 Jan;75(1):137-44. doi: 10.1111/j.1476-5381.1982.tb08766.x.

Enhanced prostacyclin production by dipyridamole in man.双嘧达莫在人体内增强前列环素的生成。

Eur J Clin Pharmacol. 1981;21(1):9-15. doi: 10.1007/BF00609581.

Cigarette smoke inhalation specifically inhibits depressor responses to prostacyclin in the rat.吸入香烟烟雾会特异性抑制大鼠体内对前列环素的降压反应。

Br J Pharmacol. 1981 May;73(1):3-5. doi: 10.1111/j.1476-5381.1981.tb16762.x.

Renal prostaglandins.肾前列腺素

Klin Wochenschr. 1982 Sep 15;60(18):1155-64. doi: 10.1007/BF01715845.

6-Keto-prostaglandin E1-stimulated bone resorption in organ culture.6-酮-前列腺素E1刺激器官培养中的骨吸收。

Calcif Tissue Int. 1984 Jul;36(4):380-3. doi: 10.1007/BF02405349.

Prostacyclin modulates cholesteryl ester hydrolytic activity by its effect on cyclic adenosine monophosphate in rabbit aortic smooth muscle cells.前列环素通过对兔主动脉平滑肌细胞中环磷酸腺苷的作用来调节胆固醇酯水解活性。

J Clin Invest. 1982 Sep;70(3):479-88. doi: 10.1172/jci110639.

Identification of 6-oxo-prostaglandin E1 as a naturally occurring prostanoid generated by rat lung.鉴定6-氧代前列腺素E1为大鼠肺产生的一种天然存在的类前列腺素。

Br J Pharmacol. 1986 Feb;87(2):327-35. doi: 10.1111/j.1476-5381.1986.tb10821.x.

Single-blind study of epoprostenol and 6-keto-prostaglandin E1 in man: effects of platelet aggregation and plasma renin.依前列醇和6-酮-前列腺素E1在人体中的单盲研究：对血小板聚集和血浆肾素的影响

Br J Clin Pharmacol. 1985 Dec;20(6):681-3. doi: 10.1111/j.1365-2125.1985.tb05128.x.

Metabolic interactions between eicosanoids in blood and vascular cells.血液和血管细胞中类二十烷酸之间的代谢相互作用。

Biochem J. 1989 Jan 15;257(2):313-20. doi: 10.1042/bj2570313.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验