2- br - α -麦角隐亭对氨基甲酸乙酯麻醉大鼠的心血管作用。

Acta physiologica latino americana Pub Date : 1982-01-01
G Pesce, F J Stefano
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引用次数: 0

摘要

本实验旨在研究溴隐亭(2- br - α -麦角隐亭)对正常血压麻醉大鼠的心血管作用。静脉给药溴隐亭(20微克/千克和200微克/千克)对平均血压和心率产生持久且非剂量依赖性的下降。对肾上腺素(一种α肾上腺素能激动剂)的加压反应被溴隐亭以剂量依赖的方式拮抗。当剂量为20微克/千克时溴隐亭表现为竞争性拮抗剂,而当剂量为200微克/千克时,溴隐亭对苯肾上腺素的反应产生不可逾越的阻断。先前给予酚妥拉明(5mg /kg)可防止溴隐亭对α肾上腺素受体的不可逾越的阻断。这一观察结果表明,这两种药物争夺同一受体。结论:阻断外周α -肾上腺素受体可能与溴隐亭对心血管的影响有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiovascular effects of 2-Br-alpha-ergocriptine in urethane anesthetized rats.

Experiments were designed to study the cardiovascular effects of Bromocriptine (2-Br-alpha-ergocriptine) in the normotensive anesthetized rats. The intravenous administration of bromocriptine (20 micrograms/kg and 200 micrograms/kg) produced a long-lasting and not dose-dependent fall in the mean blood pressure and heart rate. The pressor response to phenylephrine, an alpha adrenergic agonist, was antagonized by bromocriptine in a dose-dependent manner. At a dose of 20 micrograms/kg bromocriptine behaved as a competitive antagonist, whereas at the dose of 200 micrograms/kg produced an insurmountable blockade of the response to phenylephrine. Previous administration of phentolamine (5 mg/kg) prevented the insurmountable blockade of alpha adrenoceptors by bromocriptine. This observation suggests that both drugs compete for the same receptor. It is concluded that blockade of peripheral alpha-adrenoceptors may contribute to cardiovascular effects of bromocriptine.

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