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7-氧代前列环素在犬体内诱导出出现较晚且持久的抗缺血和抗心律失常作用。

7-oxo-PGI2 induced late appearing and long lasting antiischaemic and antiarrhythmic action in dogs.

作者信息

Végh A, Udvary E, Szekeres L, Szilvássy Z

机构信息

Department of Pharmacology, Szent-Györgyi Albert University Medical School, Szeged, Hungary.

出版信息

Biomed Biochim Acta. 1988;47(10-11):S31-4.

PMID:3073767
Abstract

In our earlier experiments administration of the stable PGI2 analogue: 7-oxo-PGI2-ephedrine salt to dogs resulted in a late-appearing and long-lasting protection from coronary ligation induced ischaemia as well as from postocclusion and reperfusion arrhythmias. Objective of the present study was to evaluate the extent and duration of antiischaemic and antiarrhythmic action induced by a single dose 50 ug/kg i.m. 7-oxo-PGI2 in dogs subjected to myocardial ischaemia evoked by left anterior descending coronary artery (LAD) ligation at different intervals (2, 6, 24, 48, 72 hours and 2 weeks) after treatment. After anaesthesia and thoracotomy the electrophysiological parameters - sinus cycle length (SCL), corrected sinus node recovery time (CSNRT), atrial and ventricular functional refractory period (AFRP, VFRP), and atrio-ventricular effective refractory period (A-V ERP) - were determined by means of computer controlled programmed electrical stimulation. Then the animals were subjected to LAD occlusion for 25 minutes and subsequent reperfusion. 7-oxo-PGI2 pretreatment considerably protected against myocardial ischaemia i.e. there was significant reduction in ST-segment elevation, the number of extrasystoles (ES) and the incidence of ventricular fibrillation (VF). The antiischaemic action started 2 or 6 hours after the drug administration, however, the maximal protection - indicated by the diminution of ischaemic epicardial ST-segment elevation - as well as the most striking reduction in postocclusion and reperfusion arrhythmias could be observed 48 hours after the single dose of 7-oxo-PGI2 and in case of two weeks treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在我们早期的实验中,给犬类施用稳定的前列环素(PGI2)类似物:7-氧代-PGI2-麻黄碱盐,可产生延迟出现且持久的保护作用,预防冠状动脉结扎诱导的缺血以及闭塞后和再灌注心律失常。本研究的目的是评估在不同时间间隔(2、6、24、48、72小时和2周)接受治疗后,单次肌肉注射50μg/kg的7-氧代-PGI2对犬类心肌缺血所诱导的抗缺血和抗心律失常作用的程度及持续时间。麻醉和开胸后,通过计算机控制的程控电刺激测定电生理参数——窦性周期长度(SCL)、校正窦房结恢复时间(CSNRT)、心房和心室功能不应期(AFRP、VFRP)以及房室有效不应期(A-V ERP)。然后使动物左前降支冠状动脉(LAD)闭塞25分钟,随后进行再灌注。7-氧代-PGI2预处理对心肌缺血有显著的保护作用,即ST段抬高、早搏(ES)数量和室颤(VF)发生率均显著降低。抗缺血作用在给药后2或6小时开始,然而,单次注射7-氧代-PGI2 48小时后以及治疗两周后,可观察到最大程度的保护作用(以缺血性心外膜ST段抬高的减轻为指标)以及闭塞后和再灌注心律失常的最显著减少。(摘要截断于250字)

相似文献

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7-oxo-PGI2 induced late appearing and long lasting antiischaemic and antiarrhythmic action in dogs.7-氧代前列环素在犬体内诱导出出现较晚且持久的抗缺血和抗心律失常作用。
Biomed Biochim Acta. 1988;47(10-11):S31-4.
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Delayed protection by 7-oxo-PGI2 against cardiac transmembrane ion shifts and early morphological changes due to ischemia and reperfusion.7-氧代前列环素对缺血再灌注引起的心脏跨膜离子转运变化及早期形态学改变的延迟性保护作用。
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7-oxo-PgI2 induced late appearing and long-lasting electrophysiological changes in the heart in situ of the rabbit, guinea-pig, dog and cat.7-氧代前列环素I2在兔、豚鼠、狗和猫的原位心脏中诱导出出现较晚且持久的电生理变化。
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