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前列腺素I2和E2对大鼠和犬冠状动脉闭塞所致心律失常的作用。

The actions of prostaglandins I2 and E2 on arrhythmias produced by coronary occlusion in the rat and dog.

作者信息

Au T L, Collins G A, Harvie C J, Walker M J

出版信息

Prostaglandins. 1979 Nov;18(5):707-20. doi: 10.1016/0090-6980(79)90091-1.

Abstract

Prostaglandins E2 and I2 were compared with known antiarrhythmics for their actions against arrhythmias produced by occlusion of the left anterior descending coronary artery in the anaesthetised rat while PGI2 was also examined in the dog. PGI2 in the dog suppressed early arrhythmias produced during occlusion but did not influence those produced by occlusion-release or those occurring 24 hours after a permanent occlusion; none of the A,B,C or D series prostaglandins tested markedly reduced 24 hour arrhythmias. In the rat PGE2 was antiarrhythmic against early occlusion arrhythmias (30 minutes occlusion) in a dose related manner (infusions of 1-4 microgram/kg/min) whereas PGI2 infusions potentiated the arrhythmogenic effect of occlusion. PGE2 was as effective an antiarrhythmic as 10mg/kg Org. 6001 which was more effective in this test situtation than dl-propranolol. No obvious mechanisms for the actions of PGE2 or PGI2 were apparent although both agents lowered blood pressure and reduced the size of the occluded zone produced by ligation.

摘要

将前列腺素E2和I2与已知抗心律失常药物进行比较,观察它们对麻醉大鼠左冠状动脉前降支闭塞所致心律失常的作用,同时也在犬身上研究了前列环素(PGI2)。犬体内的PGI2可抑制闭塞期间产生的早期心律失常,但对闭塞解除后产生的心律失常或永久性闭塞24小时后出现的心律失常无影响;所测试的A、B、C或D系列前列腺素均未显著减少24小时心律失常。在大鼠中,前列腺素E2(PGE2)以剂量相关方式(输注1 - 4微克/千克/分钟)对抗早期闭塞性心律失常(闭塞30分钟),而输注PGI2则增强了闭塞的致心律失常作用。PGE2作为抗心律失常药物的效果与10毫克/千克的Org. 6001相当,在该试验情况下,Org. 6001比dl - 普萘洛尔更有效。尽管PGE2和PGI2都能降低血压并减小结扎所致闭塞区的大小,但它们作用的明显机制并不清楚。

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