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前列环素(PGI2)对乌头碱诱发大鼠心律失常的抗心律失常作用。

The antiarrhythmic action of prostacyclin (PGI2) on aconitine induced arrhythmias in rats.

作者信息

Mest H J, Förster W

出版信息

Acta Biol Med Ger. 1978;37(5-6):827-8.

PMID:369259
Abstract

Prostacyclin (PGI2) produces an antiarrhythmic effect on aconitine induced arrhythmias in rats. The ED50 of PGI2 was 0.7 microgram/kg and the maximum antiarrhythmic effect 54 per cent. The equi-effective doses of PGE2 and PGF2alpha were higher (ED50 of PGF2alpha = 1.2 microgram/kg, ED50 of PGE2 = 2.7 microgram/kg). However, PGF2alpha and PGE2 had a maximum antiarrhythmic effect of 80 per cent in this model.

摘要

前列环素(PGI2)对乌头碱诱发的大鼠心律失常具有抗心律失常作用。PGI2的半数有效量(ED50)为0.7微克/千克,最大抗心律失常作用为54%。前列腺素E2(PGE2)和前列腺素F2α(PGF2α)的等效剂量更高(PGF2α的ED50 = 1.2微克/千克,PGE2的ED50 = 2.7微克/千克)。然而,在该模型中,PGF2α和PGE2的最大抗心律失常作用为80%。

相似文献

1
The antiarrhythmic action of prostacyclin (PGI2) on aconitine induced arrhythmias in rats.前列环素(PGI2)对乌头碱诱发大鼠心律失常的抗心律失常作用。
Acta Biol Med Ger. 1978;37(5-6):827-8.
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引用本文的文献

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International Union of Basic and Clinical Pharmacology. CIX. Differences and Similarities between Human and Rodent Prostaglandin E Receptors (EP1-4) and Prostacyclin Receptor (IP): Specific Roles in Pathophysiologic Conditions.国际基础和临床药理学联合会。CIX. 人源和啮齿动物前列腺素 E 受体(EP1-4)和前列环素受体(IP)之间的差异和相似性:在病理生理条件下的特定作用。
Pharmacol Rev. 2020 Oct;72(4):910-968. doi: 10.1124/pr.120.019331.
2
The effects of extracellular potassium, ouabain, and prostaglandins on intracellular potassium activity in sheep cardica Purkinje fibers.细胞外钾、哇巴因和前列腺素对绵羊心脏浦肯野纤维细胞内钾活性的影响。
Pflugers Arch. 1980 Nov;388(2):169-75. doi: 10.1007/BF00584124.
3
Platelet-release reaction in myocardial infarction.
心肌梗死中的血小板释放反应。
Br Med J. 1980 Mar 29;280(6218):939-40. doi: 10.1136/bmj.280.6218.939-d.
4
Prostacyclin and iloprost: equal efficiency in preserving high energy phosphates in the dog heart following coronary artery ligation.前列环素和伊洛前列素:在冠状动脉结扎后对犬心脏高能磷酸盐的保存作用中效率相同。
Basic Res Cardiol. 1987 Nov-Dec;82(6):566-75. doi: 10.1007/BF01907227.