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6-酮-前列腺素E1是一种强效的冠状动脉扩张剂,可刺激犬类的迷走神经反射。

6-Keto-prostaglandin E1 is a potent coronary vasodilator and stimulates a vagal reflex in dogs.

作者信息

Panzenbeck M J, Hintze T H, Kaley G

机构信息

Department of Physiology, New York Medical College, Valhalla.

出版信息

J Pharmacol Exp Ther. 1988 Mar;244(3):814-9.

PMID:3075239
Abstract

These studies were performed to examine the effects of 6-keto-prostaglandin E1 (6-keto-PGE1) on coronary artery blood flow and reflex cardiovascular regulation. In seven chloralose-anesthetized dogs 6-keto-PGE1 and prostacyclin (PGI2) were injected as a bolus into the left circumflex coronary artery in doses of 250 to 4000 ng. Coronary artery blood flow significantly increased and coronary artery resistance decreased in a dose-related manner. There were no significant differences observed between 6-keto-PGE1 and PGI2 in the magnitude of the maximum increase in coronary blood flow or decrease in coronary artery resistance. In six additional anesthetized dogs in which the carotid arteries were ligated in order to minimize baroreflexes, intracoronary injection of 6-keto-PGE1 and PGI2 (in doses of 7, 14 and 23 micrograms) caused systemic hypotension and bradycardia. Bilateral vagotomy attenuated the hypotension and abolished the bradycardia induced by these substances. In five conscious dogs, 6-keto-PGE1 and PGI2 were infused (2, 10 and 20 micrograms/min i.v.) for 10 min. 6-keto-PGE1 and PGI2 caused significant decreases in mean arterial pressure; however PGI2 was significantly more potent in this respect. The tachycardia to the highest doses was compared to that induced by infusion of nitroprusside (500 micrograms/min i.v.). 6-keto-PGE1 and PGI2 caused significantly less baroreflex tachycardia per millimeter of mercury decrease in arterial pressure than did nitroprusside. Thus, in anesthetized dogs, 6-keto-PGE1 and PGI2 are equipotent coronary vasodilators. These PGs also stimulate a vagal reflex which results in hypotension, bradycardia and attenuation of baroreflex-mediated tachycardia.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

进行这些研究是为了检测6-酮-前列腺素E1(6-keto-PGE1)对冠状动脉血流及反射性心血管调节的影响。在7只氯醛糖麻醉的犬中,将6-keto-PGE1和前列环素(PGI2)以250至4000 ng的剂量单次注入左旋冠状动脉。冠状动脉血流显著增加,冠状动脉阻力呈剂量依赖性降低。在冠状动脉血流最大增加幅度或冠状动脉阻力降低幅度方面,6-keto-PGE1和PGI2之间未观察到显著差异。在另外6只麻醉犬中,为尽量减少压力反射,结扎了颈动脉,冠状动脉内注射6-keto-PGE1和PGI2(剂量为7、14和23微克)导致全身低血压和心动过缓。双侧迷走神经切断术减弱了低血压,并消除了这些物质诱导的心动过缓。在5只清醒犬中,以2、10和20微克/分钟静脉输注6-keto-PGE1和PGI2 10分钟。6-keto-PGE1和PGI2导致平均动脉压显著降低;然而在这方面PGI2的作用明显更强。将最高剂量时的心动过速与硝普钠(500微克/分钟静脉输注)诱导的心动过速进行比较。与硝普钠相比,6-keto-PGE1和PGI2每降低一毫米汞柱动脉压所引起的压力反射性心动过速明显更少。因此,在麻醉犬中,6-keto-PGE1和PGI2是等效的冠状动脉血管扩张剂。这些前列腺素还刺激迷走神经反射,导致低血压、心动过缓和压力反射介导的心动过速减弱。(摘要截短于250字)

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